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<?xml-stylesheet type="text/xsl" media="screen" href="/~d/styles/rss2full.xsl"?><?xml-stylesheet type="text/css" media="screen" href="http://feeds.rsc.org/~d/styles/itemcontent.css"?><rss xmlns:a10="http://www.w3.org/2005/Atom" xmlns:feedburner="http://rssnamespace.org/feedburner/ext/1.0" version="2.0"><channel><title>RSC - Polym. Chem. latest articles</title><link>http://pubs.rsc.org/en/Journals/Journal/PY</link><description>RSC - Polym. Chem. latest articles</description><copyright>Copyright (c)  The Royal Society of Chemistry</copyright><lastBuildDate>Tue, 21 May 2013 13:16:09 Z</lastBuildDate><category>RSC - Polym. Chem. latest articles</category><image><url>http://pubs.rsc.org/content/NewImages/rsc_publishing_logo.gif</url><title>RSC - Polym. Chem. latest articles</title><link>http://pubs.rsc.org/en/Journals/Journal/PY</link></image><atom10:link xmlns:atom10="http://www.w3.org/2005/Atom" rel="self" type="application/rss+xml" href="http://feeds.rsc.org/rss/PY" /><feedburner:info uri="rss/py" /><atom10:link xmlns:atom10="http://www.w3.org/2005/Atom" rel="hub" href="http://pubsubhubbub.appspot.com/" /><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00573A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00573A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/cTqos5dUKKE/C3PY00573A</link><title>Post-modification of poly(glycidyl methacrylate)s with alkyl amine and isothiocyanate for effective pDNA delivery</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00573A, Paper&lt;/div&gt;&lt;div&gt;Cui Li, Ying-Wei Yang, Zhixiang Liang, Guolin Wu, Hui Gao&lt;br/&gt;Thiourea has been shown to interact actively with phosphate groups of DNA. To this end, linear and five-arm poly(glycidyl methacrylate)s (PGMA)s are post-modified with 1,2-ethanediamine (E), 1,4-butanediamine (B) and diethylenetriamine...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/cTqos5dUKKE" height="1" width="1"/&gt;</description><a10:updated>2013-05-21T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Cui Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ying-Wei Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhixiang Liang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guolin Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hui Gao</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00573A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00512G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00512G</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/rVmyigKCDwU/C3PY00512G</link><title>Investigating interactions between cationic particle and polyelectrolyte brushes with the Total Internal Reflection Microscopy (TIRM)</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00512G, Paper&lt;/div&gt;&lt;div&gt;To Ngai, Xiaoling Wei, Xiangjun Gong&lt;br/&gt;The manufacturing of switchable surfaces can be achieved when polymer chains are adsorbed or grafted densely on the solid surfaces. These so-called "smart" surfaces have been often used to control...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/rVmyigKCDwU" height="1" width="1"/&gt;</description><a10:updated>2013-05-21T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">To Ngai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoling Wei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiangjun Gong</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00512G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00459G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00459G</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/1018WeEddhA/C3PY00459G</link><title>Healing of carbon fibre-epoxy composites using thermoplastic additives</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00459G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00459G, Paper&lt;/div&gt;&lt;div&gt;K. Pingkarawat, T. Bhat, D. A. Craze, C. H. Wang, R. J. Varley, A. P. Mouritz&lt;br/&gt;The healing efficiency and healing mechanisms of selected insoluble thermoplastics blended into an epoxy resin and its respective carbon fibre-epoxy matrix composite is investigated.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/1018WeEddhA" height="1" width="1"/&gt;</description><a10:updated>2013-05-08T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">K. Pingkarawat</creator><creator xmlns="http://purl.org/dc/elements/1.1/">T. Bhat</creator><creator xmlns="http://purl.org/dc/elements/1.1/">D. A. Craze</creator><creator xmlns="http://purl.org/dc/elements/1.1/">C. H. Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">R. J. Varley</creator><creator xmlns="http://purl.org/dc/elements/1.1/">A. P. Mouritz</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00459G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00401E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00401E</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/iYhkuB6UhJI/C3PY00401E</link><title>Organocatalyzed controlled ROP of [small beta]-lactones towards poly(hydroxyalkanoate)s: from [small beta]-butyrolactone to benzyl [small beta]-malolactone polymers</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00401E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00401E, Paper&lt;/div&gt;&lt;div&gt;Cedric G. Jaffredo, Jean-Francois Carpentier, Sophie M. Guillaume&lt;br/&gt;[small beta]-Lactone (co)polymers. Basic organocatalysts of the guanidine (TBD), amidine (DBU) and phosphazene (BEMP) type effectively polymerize benzyl [small beta]-malolactone (MLABe) in a controlled process. Well-defined poly(3-benzyloxybutyrate)s (PMLABes) are thus formed with &lt;em&gt;M&lt;/em&gt;&lt;small&gt;&lt;sub&gt;n,NMR&lt;/sub&gt;&lt;/small&gt; up to 80 500 g mol&lt;small&gt;&lt;sup&gt;-1&lt;/sup&gt;&lt;/small&gt;. Mechanistic insights are also provided.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/iYhkuB6UhJI" height="1" width="1"/&gt;</description><a10:updated>2013-04-24T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Cedric G. Jaffredo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jean-Francois Carpentier</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sophie M. Guillaume</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00401E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00451A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00451A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/pa6lUREx1uo/C3PY00451A</link><title>Synthesis and gas permeation properties of novel spirobisindane-based polyimides of intrinsic microporosity</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00451A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00451A, Paper&lt;/div&gt;&lt;div&gt;Yulia Rogan, Ludmila Starannikova, Victoria Ryzhikh, Yuri Yampolskii, Paola Bernardo, Fabio Bazzarelli, Johannes Carolus Jansen, Neil B. McKeown&lt;br/&gt;Polyimides of intrinsic microporosity were prepared using a novel spirocyclic bisanhydride and proved highly gas permeable.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/pa6lUREx1uo" height="1" width="1"/&gt;</description><a10:updated>2013-05-17T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yulia Rogan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ludmila Starannikova</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Victoria Ryzhikh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuri Yampolskii</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Paola Bernardo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fabio Bazzarelli</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Johannes Carolus Jansen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Neil B. McKeown</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00451A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00567D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00567D</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/EoZRYW4aqwo/C3PY00567D</link><title>Stereo- and Regioselective Cyclopolymerization of Chiral 1,7-Octadiynes</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00567D, Paper&lt;/div&gt;&lt;div&gt;Joerg Unold, Dongren Wang, Wolfgang Frey, Michael Buchmeiser&lt;br/&gt;A series of diastereomeric 4,5-diethoxycarbonyl-1,7-octadiynes were synthesized from which the pure diastereomers were obtained by selective Soxhlet extraction in CHCl3. The concept of "small alkoxides" was used with varying size...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/EoZRYW4aqwo" height="1" width="1"/&gt;</description><a10:updated>2013-05-17T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Joerg Unold</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dongren Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wolfgang Frey</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michael Buchmeiser</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00567D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00404J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00404J</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/8JlrMjB_V0o/C3PY00404J</link><title>Poly([gamma]-benzyl-L-glutamate) decorated with cyanoferrate complex: synthesis, characterization and electrochemical properties</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00404J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00404J, Paper&lt;/div&gt;&lt;div&gt;Guodong Liang, Qihua Wu, Wangping Qin, Suping Bao, Fangming Zhu, Qin Wu&lt;br/&gt;New 4-armed star poly([gamma]-benzyl-&lt;small&gt;L&lt;/small&gt;-glutamate) decorated with cyanoferrate complex (PBLG-Fe) was successfully synthesized by ring-opening polymerization of [gamma]-benzyl-&lt;small&gt;L&lt;/small&gt;-glutamate, followed by a post-functionalization procedure.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/8JlrMjB_V0o" height="1" width="1"/&gt;</description><a10:updated>2013-04-19T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Guodong Liang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qihua Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wangping Qin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Suping Bao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fangming Zhu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qin Wu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00404J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00425B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00425B</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/DI4dAdJt-WY/C3PY00425B</link><title>Cationic glyco-nanogels for epidermal growth factor receptor (EGFR) specific siRNA delivery in ovarian cancer cells</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00425B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00425B, Paper&lt;/div&gt;&lt;div&gt;Marya Ahmed, Phanphen Wattanaarsakit, Ravin Narain&lt;br/&gt;Gene knockdown efficacies and cell viabilities of glyconanogels-siRNA complexes are evaluated in Hela cells at varying w/w ratios. The siRNA loaded cationic glyconanogels show effective gene knockdown efficacies in the presence and absence of serum proteins.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/DI4dAdJt-WY" height="1" width="1"/&gt;</description><a10:updated>2013-04-19T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Marya Ahmed</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Phanphen Wattanaarsakit</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ravin Narain</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00425B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00275F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00275F</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/yq8NUW1N_rI/C3PY00275F</link><title>Effects of poly(vinyl pivalate)-based stabiliser architecture on CO2-solubility and stabilising ability in dispersion polymerisation of N-vinyl pyrrolidone</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00275F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00275F, Paper&lt;/div&gt;&lt;div&gt;Natasha A. Birkin, Oliver J. Wildig, Steven M. Howdle&lt;br/&gt;We investigate the solubility and activity of PVPi-based hydrocarbon stabilisers in supercritical CO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; to compare and contrast the effect of chain length, end groups and architecture (statistical &lt;em&gt;vs.&lt;/em&gt; block copolymer) for dispersion polymerisations of &lt;em&gt;N&lt;/em&gt;-vinyl pyrrolidone.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/yq8NUW1N_rI" height="1" width="1"/&gt;</description><a10:updated>2013-05-16T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Natasha A. Birkin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Oliver J. Wildig</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Steven M. Howdle</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00275F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00534H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00534H</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/s7Z8SJ4meyE/C3PY00534H</link><title>Which Side-Reactions Compromise Nitroxide Mediated Polymerization?</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00534H, Paper&lt;/div&gt;&lt;div&gt;Ganna Gryn'ova, Ching Yeh Lin, Michelle L Coote&lt;br/&gt;The mechanism of the nitroxide mediated polymerization (NMP) is well understood, however less is known about the side-reactions that interfere and in certain cases severely compromise it. Experimental studies inevitably...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/s7Z8SJ4meyE" height="1" width="1"/&gt;</description><a10:updated>2013-05-16T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ganna Gryn'ova</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ching Yeh Lin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michelle L Coote</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00534H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00505D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00505D</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/l_yMSlalK8M/C3PY00505D</link><title>Facile synthesis of poly(3-hexylthiophene)-block-poly(ethylene oxide) copolymers via Steglich esterification</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00505D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00505D, Communication&lt;/div&gt;&lt;div&gt;Harikrishna Erothu, Arun A. Sohdi, Anitha C. Kumar, Andrew J. Sutherland, Christine Dagron-Lartigau, Ahmed Allal, Roger C. Hiorns, Paul D. Topham&lt;br/&gt;Poly(ethylene oxide) has been attached to poly(3-hexylthiophene) using metal-free coupling to produce pure diblock copolymers, highly relevant for use in organic electronic devices.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/l_yMSlalK8M" height="1" width="1"/&gt;</description><a10:updated>2013-05-13T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Harikrishna Erothu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Arun A. Sohdi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anitha C. Kumar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrew J. Sutherland</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christine Dagron-Lartigau</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ahmed Allal</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Roger C. Hiorns</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Paul D. Topham</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00505D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00409K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00409K</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/uMZOxG1zKh0/C3PY00409K</link><title>Synthesis of end-functionalized phosphate and phosphonate-polypeptides by ring-opening polymerization of their corresponding N-carboxyanhydride</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00409K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00409K, Communication&lt;/div&gt;&lt;div&gt;Soumen Das, Mrityunjoy Kar, Sayam Sen Gupta&lt;br/&gt;Phosphopolypeptides provide an interesting biomimetic analog for phosphorylated proteins that are involved in biomineralization.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/uMZOxG1zKh0" height="1" width="1"/&gt;</description><a10:updated>2013-05-07T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Soumen Das</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mrityunjoy Kar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sayam Sen Gupta</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00409K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00377A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00377A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/2lyMmtPDX5Q/C3PY00377A</link><title>Synthesis of high refractive index and low-birefringence acrylate polymers with a tetraphenylethane skeleton in the side chain</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00377A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00377A, Paper&lt;/div&gt;&lt;div&gt;Yusuke Tojo, Yuki Arakwa, Junji Watanabe, Gen-ichi Konishi&lt;br/&gt;We report new acrylate polymers possessing a tetraphenylethane skeleton in the side chain that exhibit a high refractive index and low-birefringence.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/2lyMmtPDX5Q" height="1" width="1"/&gt;</description><a10:updated>2013-04-26T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yusuke Tojo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuki Arakwa</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Junji Watanabe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gen-ichi Konishi</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00377A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00437F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00437F</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/VSOcWjKtHkI/C3PY00437F</link><title>Unsaturated poly(phosphoester)s via ring-opening metathesis polymerization</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00437F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00437F, Paper&lt;/div&gt;&lt;div&gt;Tobias Steinbach, Evandro M. Alexandrino, Frederik R. Wurm&lt;br/&gt;The first report on ring-opening metathesis polymerization to unsaturated poly(phosphoester)s is presented. Novel seven-membered phosphates were synthesized and polymerization and copolymerization with cyclooctene were established to produce potentially biodegradable poly(phosphoester)s.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/VSOcWjKtHkI" height="1" width="1"/&gt;</description><a10:updated>2013-04-24T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Tobias Steinbach</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Evandro M. Alexandrino</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Frederik R. Wurm</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00437F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00548H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00548H</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/lxXzibCvlE0/C3PY00548H</link><title>Protected N-Heterocyclic Carbenes as Latent Pre-Catalysts for the Polymerization of ε-Caprolactone</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00548H, Paper&lt;/div&gt;&lt;div&gt;Stefan Naumann, Friedrich Schmidt, Wolfgang Frey, Michael Buchmeiser&lt;br/&gt;Various protected N-heterocyclic carbenes (NHCs) were synthesized and used as latent pre-catalysts in the solvent-free polymerization of ε-caprolactone (ε-CL) in the presence of benzylic alcohol (Bn-OH). The range of investigated...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/lxXzibCvlE0" height="1" width="1"/&gt;</description><a10:updated>2013-05-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Stefan Naumann</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Friedrich Schmidt</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wolfgang Frey</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michael Buchmeiser</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00548H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00501A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00501A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/2Bye3XkMEEg/C3PY00501A</link><title>Effect of Furan [small pi]-bridge on Polymer Coplanarity and Performance in Organic Field Effect Transistors</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00501A, Paper&lt;/div&gt;&lt;div&gt;Jianyu Yuan, Yaping Zang, Huilong Dong, Guojun Liu, Chongan Di, Youyong Li, Wanli Ma&lt;br/&gt;An existing donor-acceptor polymer was modified by introducing a furan [small pi]-bridge to its backbone, aiming to extend the [small pi]-conjugation and achieve higher performance in organic field effect transistors (OFETs). The...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/2Bye3XkMEEg" height="1" width="1"/&gt;</description><a10:updated>2013-05-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jianyu Yuan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yaping Zang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huilong Dong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guojun Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chongan Di</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Youyong Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wanli Ma</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00501A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00496A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00496A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/6z8TZlvgPxg/C3PY00496A</link><title>pH-responsive poly(4-hydroxybenzoyl methacrylates) - design and engineering of intelligent drug delivery nanovectors</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00496A, Paper&lt;/div&gt;&lt;div&gt;Francesca Mastrotto, Stefano Salmaso, Yi Lin Lee, Cameron Alexander, Paolo Caliceti, Giuseppe Mantovani&lt;br/&gt;This is an Accepted Manuscript, which has been through the RSC Publishing peer review process and has been accepted for publication. Accepted manuscripts are published online shortly after acceptance. This version of the article will be replaced by the fully edited, formatted and proof read Advance Article as soon as this is available.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/6z8TZlvgPxg" height="1" width="1"/&gt;</description><a10:updated>2013-05-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Francesca Mastrotto</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stefano Salmaso</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yi Lin Lee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cameron Alexander</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Paolo Caliceti</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Giuseppe Mantovani</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00496A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00553D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00553D</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/k65ZvNyEYT4/C3PY00553D</link><title>A new insight of Biginelli reaction: the dawn of multicomponent click chemistry?</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00553D, Paper&lt;/div&gt;&lt;div&gt;Chongyu Zhu, Bin Yang, Yuan Zhao, Changkui Fu, Lei Tao, Yen Wei&lt;br/&gt;Looking at 'old' reactions from new perspectives sometimes brings new breakthroughs in current hot research areas. The successful multicomponent reactions (MCRs) in organic chemistry are therefore reinvestigated, and we are...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/k65ZvNyEYT4" height="1" width="1"/&gt;</description><a10:updated>2013-05-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Chongyu Zhu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bin Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuan Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Changkui Fu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lei Tao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yen Wei</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00553D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00474K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00474K</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/-Yr6PA3cano/C3PY00474K</link><title>Synthesis of [small alpha]-Helix-Containing PPEGMEA-g-PBLG Well-Defined Amphiphilic Graft Copolymer by Sequential SET-LRP and ROP</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00474K, Paper&lt;/div&gt;&lt;div&gt;Sujuan Zhai, Xuemei Song, Chun Feng, Xiuyu Jiang, Yongjun Li, Guolin Lu, Xiaoyu Huang&lt;br/&gt;A series of well-defined polypeptide-based amphiphilic graft copolymers containing hydrophilic poly(poly(ethylene glycol) methyl ether acrylate) (PPEGMEA) backbone and hydrophobic poly([gamma]-benzyl-L-glutamate) (PBLG) side chains was synthesized by successive single electron transfer-living...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/-Yr6PA3cano" height="1" width="1"/&gt;</description><a10:updated>2013-05-14T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sujuan Zhai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xuemei Song</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chun Feng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiuyu Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yongjun Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guolin Lu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoyu Huang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00474K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00478C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00478C</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/44HeUNTOa8c/C3PY00478C</link><title>Tunable thermo-, pH- and light-responsive copolymer micelles</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00478C, Communication&lt;/div&gt;&lt;div&gt;Weizhong Yuan, Wen Guo, Hui Zou, Jie Ren&lt;br/&gt;Novel amphiphilic block copolymer containing N,N-dimethylaminoethyl and azopyridine groups has been synthesized and self-assembled into micelles with triple tunable responses to temperature, pH and light from shell to core of...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/44HeUNTOa8c" height="1" width="1"/&gt;</description><a10:updated>2013-05-14T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Weizhong Yuan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wen Guo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hui Zou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jie Ren</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00478C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00319A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00319A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/wI2vJE_8Gzc/C3PY00319A</link><title>Revisiting the long-chain branch formation mechanism in metallocene catalyzed polyethylenes</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00319A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00319A, Paper&lt;/div&gt;&lt;div&gt;Vahid Karimkhani, Faramarz Afshar-Taromi, Saeed Pourmahdian, Florian J. Stadler&lt;br/&gt;The effect of polymerization parameters on several long-chain branched (LCB) ethylene homopolymers and ethylene/[small alpha]-olefin copolymers was investigated with respect to their degree of long-chain branching. It is concluded that auto-copolymerisation mechanism and potentially [sigma]-bond metathesis are the responsible mechanisms for LCB-formation.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/wI2vJE_8Gzc" height="1" width="1"/&gt;</description><a10:updated>2013-04-22T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Vahid Karimkhani</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Faramarz Afshar-Taromi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Saeed Pourmahdian</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Florian J. Stadler</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00319A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00433C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00433C</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/_UnL6GncwNE/C3PY00433C</link><title>Conjugated poly(azomethine)s via simple one-step polycondensation chemistry: synthesis, thermal and optoelectronic properties</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00433C, Paper&lt;/div&gt;&lt;div&gt;Michiel Petrus, Ricardo Bouwer, Ugo Lafont, Krishna Murthy, Rene Kist, Marcus Bohm, Yoann Olivier, Tom J Savenije, Laurens Siebbeles, N C Greenham, Theo J. Dingemans&lt;br/&gt;Three conjugated triphenylamine-based poly(azomethine)s were prepared via well-known polycondensation chemistry using cheap and readily available starting materials and the results were contrasted with rrP3HT. Three functionalized diaminetriphenylamines (TPA(X), X= -H,...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/_UnL6GncwNE" height="1" width="1"/&gt;</description><a10:updated>2013-05-13T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Michiel Petrus</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ricardo Bouwer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ugo Lafont</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Krishna Murthy</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rene Kist</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Marcus Bohm</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yoann Olivier</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tom J Savenije</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Laurens Siebbeles</creator><creator xmlns="http://purl.org/dc/elements/1.1/">N C Greenham</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Theo J. Dingemans</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00433C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00500C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00500C</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/Z66yPFCRHOk/C3PY00500C</link><title>Linkage and Acceptor Effect on Diverse Memory Behavior of Triphenylamine-Based Aromatic Polymers</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00500C, Paper&lt;/div&gt;&lt;div&gt;Guey-Sheng Liou, Chih-Jung Chen, Yi-Cheng Hu&lt;br/&gt;New functional triphenylamine-based (TPA-based) aromatic polyether OXPE and polyester 6FPET were synthesized and used for memory device application. To get more insight into the relationship between linkage group and memory...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/Z66yPFCRHOk" height="1" width="1"/&gt;</description><a10:updated>2013-05-13T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Guey-Sheng Liou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chih-Jung Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yi-Cheng Hu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00500C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00321C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00321C</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/EbuPE7SfddI/C3PY00321C</link><title>Single chain polymer nanoparticles via sequential ATRP and oxidative polymerization</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00321C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00321C, Paper&lt;/div&gt;&lt;div&gt;Philip T. Dirlam, Hyo Ju Kim, Kyle J. Arrington, Woo Jin Chung, Rabindra Sahoo, Lawrence J. Hill, Philip J. Costanzo, Patrick Theato, Kookheon Char, Jeffrey Pyun&lt;br/&gt;The use of a novel 3,4-propylenedioxythiophene styrenic monomer is reported to prepare single chain polymeric nanoparticles with conjugated electroactive inclusions.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/EbuPE7SfddI" height="1" width="1"/&gt;</description><a10:updated>2013-05-07T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Philip T. Dirlam</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hyo Ju Kim</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kyle J. Arrington</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Woo Jin Chung</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rabindra Sahoo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lawrence J. Hill</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Philip J. Costanzo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Patrick Theato</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kookheon Char</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jeffrey Pyun</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00321C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00362K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00362K</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/6TXosaujSwc/C3PY00362K</link><title>Comparing solution and melt-state association of hydrogen bonds in supramolecular polymers</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00362K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00362K, Paper&lt;/div&gt;&lt;div&gt;Florian Herbst, Wolfgang H. Binder&lt;br/&gt;Mono- and bifunctional poly(&lt;em&gt;n&lt;/em&gt;-butyl acrylate)s (PnBAs) bearing different hydrogen bonding motifs (thymine (THY) or 2,6-diaminotriazine (DAT)) were prepared by a combination of atom transfer radical polymerization (ATRP) and azide/alkyne "click"-reaction to investigate the association of hydrogen bonding motifs in solution (toluene-d&lt;small&gt;&lt;sub&gt;8&lt;/sub&gt;&lt;/small&gt;) and in the melt state.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/6TXosaujSwc" height="1" width="1"/&gt;</description><a10:updated>2013-04-19T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Florian Herbst</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wolfgang H. Binder</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00362K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00250K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00250K</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/J4GEQAacqfE/C3PY00250K</link><title>Polypyrrole-silver composites prepared by the reduction of silver ions with polypyrrole nanotubes</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00250K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00250K, Paper&lt;/div&gt;&lt;div&gt;Jitka Skodova, Dusan Kopecky, Martin Vrnata, Martin Varga, Jan Prokes, Miroslav Cieslar, Patrycja Bober, Jaroslav Stejskal&lt;br/&gt;The synthesis and characterization of nanocomposites containing polypyrrole and silver particles &lt;em&gt;via&lt;/em&gt; reaction of the previously synthesized polymer with an aqueous solution of silver nitrate.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/J4GEQAacqfE" height="1" width="1"/&gt;</description><a10:updated>2013-04-05T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jitka Skodova</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dusan Kopecky</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Martin Vrnata</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Martin Varga</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jan Prokes</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Miroslav Cieslar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Patrycja Bober</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jaroslav Stejskal</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00250K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00396E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00396E</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/cbSP_L60AJc/C3PY00396E</link><title>Dithioketopyrrolopyrrole (DTPP)-based conjugated polymers prepared upon thionation with Lawesson's reagent</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00396E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00396E, Paper&lt;/div&gt;&lt;div&gt;Irina Welterlich, Bernd Tieke&lt;br/&gt;A one-step thionation approach is presented which converts DPP-polymers into DTPP-polymers, which exhibit red-shifted absorption and lower bandgap.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/cbSP_L60AJc" height="1" width="1"/&gt;</description><a10:updated>2013-05-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Irina Welterlich</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bernd Tieke</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00396E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00359K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00359K</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/OHCr34SPsC0/C3PY00359K</link><title>Thiourea-Functionalized Poly(phenyleneethynylene): Fluorescent Chemosensors for Anions and Cations</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00359K, Paper&lt;/div&gt;&lt;div&gt;Xue Yong, Wen Wan, Mingjian Su, Wenwei You, Xinwei Lu, Yichen Yan, Jinqing Qu, Ruiyuan Liu&lt;br/&gt;A novel poly(phenyleneethynylene)-containing thiourea groups [poly(1)] was synthesized. The anion sensing ability of poly(1) was assessed using tetra-n-butylammonium (TBA) salts of a series of anions in DMF. The addition of...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/OHCr34SPsC0" height="1" width="1"/&gt;</description><a10:updated>2013-05-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xue Yong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wen Wan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mingjian Su</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wenwei You</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xinwei Lu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yichen Yan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jinqing Qu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ruiyuan Liu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00359K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00443K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00443K</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/w0O_Rix2ilA/C3PY00443K</link><title>Efficient method to synthesize vinyl ethers (VEs) that bear various halogenated or functional groups and their radical copolymerization with chlorotrifluoroethylene (CTFE) to yield functional poly(VE-alt-CTFE) alternated copolymers</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00443K, Paper&lt;/div&gt;&lt;div&gt;Ali Alaaeddine, Guillaume Couture, Bruno Ameduri&lt;br/&gt;An air-stable palladium catalyst formed in situ from commercially available components efficiently catalyzed the transetherification between ethyl vinyl ether and various alcohols to lead to the corresponding original vinyl ethers...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/w0O_Rix2ilA" height="1" width="1"/&gt;</description><a10:updated>2013-05-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ali Alaaeddine</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guillaume Couture</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bruno Ameduri</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00443K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00350G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00350G</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/cEBTIWUGooA/C3PY00350G</link><title>Fluorescence turn-on detection of DNA based on the aggregation-induced emission of conjugated poly(pyridinium salt)s</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00350G, Paper&lt;/div&gt;&lt;div&gt;Yan Lu, Jingfen Sun, Lei Wang, Dandan Cheng, Yujiao Sun, Xianshun Zeng&lt;br/&gt;This is an Accepted Manuscript, which has been through the RSC Publishing peer review process and has been accepted for publication. Accepted manuscripts are published online shortly after acceptance. This version of the article will be replaced by the fully edited, formatted and proof read Advance Article as soon as this is available.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/cEBTIWUGooA" height="1" width="1"/&gt;</description><a10:updated>2013-05-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yan Lu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jingfen Sun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lei Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dandan Cheng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yujiao Sun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xianshun Zeng</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00350G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00511A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00511A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/g5Z62cRETAE/C3PY00511A</link><title>Electrografting onto ITO substrates of poly(thiophene)-based micelles decorated by acrylate groups</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00511A, Paper&lt;/div&gt;&lt;div&gt;Farid Ouhib, Simon Desbief, Roberto Lazzaroni, Sorin Melinte, Augustin Dutu, Christine Jerome, Christophe Detrembleur&lt;br/&gt;We report on a simple process for the chemisorption of poly(thiophene)-based block copolymers onto ITO substrates. Two poly(thiophene) block copolymers functionalized by acrylates on the second block are prepared by...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/g5Z62cRETAE" height="1" width="1"/&gt;</description><a10:updated>2013-05-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Farid Ouhib</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Simon Desbief</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Roberto Lazzaroni</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sorin Melinte</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Augustin Dutu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christine Jerome</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christophe Detrembleur</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00511A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00460K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00460K</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/dgqfY01-6jI/C3PY00460K</link><title>Self-Assembly of Amphiphilic Random Co-poly(ionic liquid)s: the Effect of Anions, Molecular Weight, and Molecular Weight Distribution</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00460K, Paper&lt;/div&gt;&lt;div&gt;Jiangna Guo, Yinxia Zhou, Lihua Qiu, Chao Yuan, Feng Yan&lt;br/&gt;Self-assembly behavior of amphiphilic random co-poly(ionic liquid)s in aqueous solution was investigated in this work. An imidazolium-type homopolymer, poly(1-(4-vinylbenzyl)-3-methyl imidazolium chloride) (denoted as PIL-[Cl]), was synthesized via reversible addition fragmentation...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/dgqfY01-6jI" height="1" width="1"/&gt;</description><a10:updated>2013-05-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jiangna Guo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yinxia Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lihua Qiu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chao Yuan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Feng Yan</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00460K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00423F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00423F</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/4WJMUKbqGkw/C3PY00423F</link><title>Enhanced thermal stability of organic solar cells by using photolinkable end-capped polythiophenes</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00423F, Paper&lt;/div&gt;&lt;div&gt;Sokha Khiev, Lionel Derue, Getachew Ayenew, Hussein Medlej, Ross Brown, Laurent Rubatat, Roger C Hiorns, Guillaume Wantz, Christine Dagron-Lartigau&lt;br/&gt;The use of poly(3-hexylthiophene) (P3HT) end-capped with anthracene (P3HT-A) in a blend with [6,6]-phenyl C61 butyric acid methyl ester (PCBM) is demonstrated to physically stabilize bulk-heterojunction photovoltaic solar cells. Bulk...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/4WJMUKbqGkw" height="1" width="1"/&gt;</description><a10:updated>2013-05-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sokha Khiev</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lionel Derue</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Getachew Ayenew</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hussein Medlej</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ross Brown</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Laurent Rubatat</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Roger C Hiorns</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guillaume Wantz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christine Dagron-Lartigau</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00423F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00397C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00397C</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/FdlC1wlnhCM/C3PY00397C</link><title>Macromolecular engineering via ring-opening polymerization (2): L-lactide/trimethylene carbonate copolymerization - kinetic and microstructural control via catalytic tuning</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00397C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00397C, Paper&lt;/div&gt;&lt;div&gt;William Guerin, Marion Helou, Martine Slawinski, Jean-Michel Brusson, Sophie M. Guillaume, Jean-Francois Carpentier&lt;br/&gt;Copolymerization of &lt;small&gt;L&lt;/small&gt;-LA and TMC has been achieved with binary systems, associating either a metal-based (pre)catalyst or an organocatalyst with benzyl alcohol.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/FdlC1wlnhCM" height="1" width="1"/&gt;</description><a10:updated>2013-04-19T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">William Guerin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Marion Helou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Martine Slawinski</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jean-Michel Brusson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sophie M. Guillaume</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jean-Francois Carpentier</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00397C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00343D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00343D</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/CtB-G0Sn5bw/C3PY00343D</link><title>Synthesis and applications of unsaturated cyclocarbonates</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00343D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00343D, Review Article&lt;/div&gt;&lt;div&gt;Vincent Besse, Fatou Camara, Coline Voirin, Remi Auvergne, Sylvain Caillol, Bernard Boutevin&lt;br/&gt;Great attention has always been paid to monomers bearing at least two reactive groups, one for copolymerization and one for further reaction, in particular, for cross-linking.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/CtB-G0Sn5bw" height="1" width="1"/&gt;</description><a10:updated>2013-04-19T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Vincent Besse</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fatou Camara</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Coline Voirin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Remi Auvergne</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sylvain Caillol</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bernard Boutevin</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00343D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00426K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00426K</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/UCGsSr_G5Ik/C3PY00426K</link><title>RAFT polymerization of dimethyl(methacryloyloxy)methyl phosphonate and its phosphonic acid derivative: a new opportunity for phosphorus-based materials</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00426K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00426K, Paper&lt;/div&gt;&lt;div&gt;Benjamin Canniccioni, Sophie Monge, Ghislain David, Jean-Jacques Robin&lt;br/&gt;RAFT polymerization of dimethyl(methacryloyloxy)methyl phosphonate (MAPC1) and hydrolyzed MAPC1 was achieved in DMF at 70 [degree]C.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/UCGsSr_G5Ik" height="1" width="1"/&gt;</description><a10:updated>2013-04-19T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Benjamin Canniccioni</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sophie Monge</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ghislain David</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jean-Jacques Robin</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00426K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00309D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00309D</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/lPm6sakshVs/C3PY00309D</link><title>A highly active homogeneous ICAR ATRP of methyl methacrylate using ppm levels of organocopper catalyst</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00309D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00309D, Paper&lt;/div&gt;&lt;div&gt;Ting Guo, Lifen Zhang, Xiangqiang Pan, Xiaohong Li, Zhenping Cheng, Xiulin Zhu&lt;br/&gt;A highly active homogeneous ICAR ATRP of MMA was successfully carried out in bulk, using several ppm concentration of organocopper Cu(SC(S)N(C&lt;small&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;/small&gt;H&lt;small&gt;&lt;sub&gt;9&lt;/sub&gt;&lt;/small&gt;)&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;)&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; or Cu(SeC(Se)N(C&lt;small&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;/small&gt;H&lt;small&gt;&lt;sub&gt;9&lt;/sub&gt;&lt;/small&gt;)&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;)&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; as the catalyst.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/lPm6sakshVs" height="1" width="1"/&gt;</description><a10:updated>2013-04-19T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ting Guo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lifen Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiangqiang Pan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaohong Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhenping Cheng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiulin Zhu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00309D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00172E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00172E</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/Ybpx0Vmh0C0/C3PY00172E</link><title>Molecular design of environmentally benign segmented polyurethane(urea)s: effect of the hard segment component on the molecular aggregation states and biodegradation behavior</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00172E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00172E, Paper&lt;/div&gt;&lt;div&gt;Yoshihiko Oniki, Ken Suzuki, Yuji Higaki, Ryohei Ishige, Noboru Ohta, Atsushi Takahara&lt;br/&gt;We investigated the molecular aggregation states, mechanical properties, and biodegradability of environmentally benign segmented polyurethane(urea)s [SPU(U)s] with an [small alpha]-amino acid lysine-based diisocyanate (LDI).&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/Ybpx0Vmh0C0" height="1" width="1"/&gt;</description><a10:updated>2013-04-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yoshihiko Oniki</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ken Suzuki</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuji Higaki</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ryohei Ishige</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Noboru Ohta</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Atsushi Takahara</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00172E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00375B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00375B</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/oPDqanZrCgU/C3PY00375B</link><title>Synthesis and ring-opening polymerisation of a new alkyne-functionalised glycolide towards biocompatible amphiphilic graft copolymers</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00375B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00375B, Paper&lt;/div&gt;&lt;div&gt;Fanny Coumes, Vincent Darcos, Dominique Domurado, Suming Li, Jean Coudane&lt;br/&gt;New "clickable" polyesters bearing pendant alkyne groups were used to prepare amphiphilic block copolymers based on polyesters.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/oPDqanZrCgU" height="1" width="1"/&gt;</description><a10:updated>2013-04-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Fanny Coumes</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Vincent Darcos</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dominique Domurado</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Suming Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jean Coudane</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00375B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00119A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00119A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/uqxCl-noh-o/C3PY00119A</link><title>Synthesis, characterization and photovoltaic properties of poly(cyclopentadithiophene-alt-isoindigo)</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00119A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00119A, Paper&lt;/div&gt;&lt;div&gt;Chun-Chih Ho, Sheng-Yung Chang, Tzu-Chia Huang, Chien-Ann Chen, Hsueh-Chung Liao, Yang-Fang Chen, Wei-Fang Su&lt;br/&gt;The side chain structure of isoindigo copolymers plays a major role in determining the photovoltaic performance. The branch chain is more effective than the linear chain to have required nanomorphology for high efficiency solar cells.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/uqxCl-noh-o" height="1" width="1"/&gt;</description><a10:updated>2013-04-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Chun-Chih Ho</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sheng-Yung Chang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tzu-Chia Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chien-Ann Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hsueh-Chung Liao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yang-Fang Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wei-Fang Su</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00119A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00299C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00299C</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/2sMsXNbAQUo/C3PY00299C</link><title>Unprecedented scissor effect of macromolecular cross-linkers on the glass transition temperature of poly(N-vinylimidazole), crystallinity suppression of poly(tetrahydrofuran) and molecular mobility by solid state NMR in poly(N-vinylimidazole)-l-poly(tetrahydrofuran) conetworks</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00299C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00299C, Paper&lt;/div&gt;&lt;div&gt;Csaba Fodor, Attila Domjan, Bela Ivan&lt;br/&gt;A scissor effect for glass transition with Fox-Flory relation (&lt;em&gt;T&lt;/em&gt;&lt;small&gt;&lt;sub&gt;g&lt;/sub&gt;&lt;/small&gt; [similar] 1/&lt;em&gt;M&lt;/em&gt;&lt;small&gt;&lt;sub&gt;c&lt;/sub&gt;&lt;/small&gt;) and crystallisation suppression of cross-linker exist in polymer conetworks with immiscible chains.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/2sMsXNbAQUo" height="1" width="1"/&gt;</description><a10:updated>2013-04-03T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Csaba Fodor</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Attila Domjan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bela Ivan</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00299C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00533J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00533J</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/9Ghs_Nz0m4g/C3PY00533J</link><title>Light-Responsive Linear-Dendritic Amphiphiles and Their Nanomedicines for NIR-Triggered Drug Release</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00533J, Paper&lt;/div&gt;&lt;div&gt;Lin Sun, Bangshang Zhu, Yue Su, C Dong&lt;br/&gt;Both ultraviolet (UV) and near-infrared (NIR) light-responsive linear-dendritic amphiphiles PEO-D3DNQ were click conjugated by connecting diazonaphthoquinone (DNQ)-decorated poly(amido amine) dendron D3 (generation 3) and linear poly(ethylene oxide) (PEO) with molecular...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/9Ghs_Nz0m4g" height="1" width="1"/&gt;</description><a10:updated>2013-05-08T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Lin Sun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bangshang Zhu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yue Su</creator><creator xmlns="http://purl.org/dc/elements/1.1/">C Dong</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00533J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00382E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00382E</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/SAcqDc2W2Is/C3PY00382E</link><title>Facile Synthesis of Multi-block Copolymers Containing Poly(ester-amide) Segments with Ordered Side Group Sequence</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00382E, Communication&lt;/div&gt;&lt;div&gt;An Lv, Xin-Xing Deng, Lei Li, Zi-Long Li, Yao-Zong Wang, Fu-Sheng Du, Zichen Li&lt;br/&gt;We report a facile method for the synthesis of multi-block copolymers consisting of poly (ethylene glycol) (PEG) and poly(ester-amide) segments with ordered side group sequence via multicomponent polymerization based on...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/SAcqDc2W2Is" height="1" width="1"/&gt;</description><a10:updated>2013-05-08T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">An Lv</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xin-Xing Deng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lei Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zi-Long Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yao-Zong Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fu-Sheng Du</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zichen Li</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00382E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00427A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00427A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/2zSI45Y-GZI/C3PY00427A</link><title>UV-induced functionalization of poly(divinylbenzene) nanoparticles via efficient [2+2] cycloadditions</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00427A, Paper&lt;/div&gt;&lt;div&gt;Anitha Ethirajan, Linny Baeten, Matthias Conradi, Kayte Ranieri, Bert  Conings , Boyen Hans-Gerd, Thomas Junkers&lt;br/&gt;The efficient functionalization of poly(divinyl)benzene (polyDVB) nanoparticles via Paterno-Buchi type [2+2] photocycloadditions is described. Initially polyDVB nanoparticles with high density of alkene groups on the surface are synthesized via radical...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/2zSI45Y-GZI" height="1" width="1"/&gt;</description><a10:updated>2013-05-08T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Anitha Ethirajan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Linny Baeten</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Matthias Conradi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kayte Ranieri</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bert  Conings </creator><creator xmlns="http://purl.org/dc/elements/1.1/">Boyen Hans-Gerd</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Thomas Junkers</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00427A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00394A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00394A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/veGAKgM6FGc/C3PY00394A</link><title>Control of the chemistry outside the pore in honeycomb patterned films</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00394A, Paper&lt;/div&gt;&lt;div&gt;Alberto S de Leon, Adolfo del Campo, Christine Labrugere, Marta Fernandez-Garcia, Alexandra Munoz-Bonilla, Juan  Rodriguez-Hernandez&lt;br/&gt;We report the selective functionalization of the external surface in honeycomb structured porous films while maintaining the functionality of the pore. For that purpose, we describe the preparation of polymer...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/veGAKgM6FGc" height="1" width="1"/&gt;</description><a10:updated>2013-05-08T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Alberto S de Leon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Adolfo del Campo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christine Labrugere</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Marta Fernandez-Garcia</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alexandra Munoz-Bonilla</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Juan  Rodriguez-Hernandez</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00394A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00390F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00390F</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/RXwST8Y140I/C3PY00390F</link><title>Synthesis of random copolymer based pH-responsive nanoparticles as drug carriers for cancer therapeutics</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00390F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00390F, Paper&lt;/div&gt;&lt;div&gt;Apiradee Honglawan, Houping Ni, Drew Weissman, Shu Yang&lt;br/&gt;Facile and versatile fabrication of pH-responsive nanoparticles (NPs) based on amphiphilic random copolymers as novel drug carriers for chemotherapy.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/RXwST8Y140I" height="1" width="1"/&gt;</description><a10:updated>2013-05-08T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Apiradee Honglawan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Houping Ni</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Drew Weissman</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shu Yang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00390F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00499F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00499F</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/6UhWoksCWKk/C3PY00499F</link><title>Organic Microporous Polymer from Hexaphenylbenzene Based Triptycene Monomer: Synthesis and Its Gas Storage Properties</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00499F, Communication&lt;/div&gt;&lt;div&gt;Chun Zhang, Lian-Hui Peng, Buyi Li, Ying Liu, Peng-Cheng Zhu, Zhen Wang, Deng-Huang Zhan, Bien Tan, Xiang-Liang Yang, Hui-Bi Xu&lt;br/&gt;A novel organic microporous polymer (HTP) has been synthesized from hexaphenylbenzene based triptycene monomer by Ni(0)-catalyzed Ullmann cross-coupling reaction, which displays the BET surface area of 1151 m2 g-1 and...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/6UhWoksCWKk" height="1" width="1"/&gt;</description><a10:updated>2013-05-08T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Chun Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lian-Hui Peng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Buyi Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ying Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Peng-Cheng Zhu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhen Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Deng-Huang Zhan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bien Tan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiang-Liang Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hui-Bi Xu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00499F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00487B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00487B</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/nawtzx14zC4/C3PY00487B</link><title>The reactivity of N-vinylcarbazole in RAFT polymerization: trithiocarbonates deliver optimal control for the synthesis of homopolymers and block copolymers</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00487B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00487B, Paper&lt;/div&gt;&lt;div&gt;Daniel J. Keddie, Carlos Guerrero-Sanchez, Graeme Moad&lt;br/&gt;The use of various RAFT agents including dithiobenzoates, trithiocarbonates, xanthates, and conventional and switchable &lt;em&gt;N&lt;/em&gt;-aryldithiocarbamates in RAFT polymerization of &lt;em&gt;N&lt;/em&gt;-vinylcarbazole has been explored with a view to establishing which is most effective.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/nawtzx14zC4" height="1" width="1"/&gt;</description><a10:updated>2013-04-30T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Daniel J. Keddie</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Carlos Guerrero-Sanchez</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Graeme Moad</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00487B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00365E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00365E</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/JIlqJBty9Ww/C3PY00365E</link><title>Phosphonium ionenes from well-defined step-growth polymerization: thermal and melt rheological properties</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00365E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00365E, Paper&lt;/div&gt;&lt;div&gt;Sean T. Hemp, Musan Zhang, Mana Tamami, Timothy E. Long&lt;br/&gt;A novel family of phosphonium ionenes was synthesized using step-growth polymerization, and they displayed excellent thermal and chemical stabilities.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/JIlqJBty9Ww" height="1" width="1"/&gt;</description><a10:updated>2013-04-23T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sean T. Hemp</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Musan Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mana Tamami</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Timothy E. Long</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00365E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00285C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00285C</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/YDoLe0kDGLc/C3PY00285C</link><title>Organoselenium compounds: development of a universal "living" free radical polymerization mediator</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00285C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00285C, Communication&lt;/div&gt;&lt;div&gt;Jindong Zeng, Jian Zhu, Xiangqiang Pan, Zhengbiao Zhang, Nianchen Zhou, Zhenping Cheng, Wei Zhang, Xiulin Zhu&lt;br/&gt;A new versatile mediator for conducting "living" radical polymerization was developed based on diselenocarbonyl compounds.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/YDoLe0kDGLc" height="1" width="1"/&gt;</description><a10:updated>2013-04-19T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jindong Zeng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jian Zhu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiangqiang Pan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhengbiao Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nianchen Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhenping Cheng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wei Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiulin Zhu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00285C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00255A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00255A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/v-p9LPbXglo/C3PY00255A</link><title>Hydrogen bonding assisted reversible-deactivation radical copolymerization of 4-vinylpyridine and styrene: a facile approach for adjusting polymerization behavior, polymer composition, etc.</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00255A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00255A, Paper&lt;/div&gt;&lt;div&gt;Xiaoji Zhou, Wenxiang Wang, Huali Yu, Junfei Zhao, Zhengbiao Zhang, Xiulin Zhu&lt;br/&gt;Reversible-deactivation radical copolymerization of 4-vinylpyridine (4VP) and styrene (St) was performed in a hydrogen bonding donor solvent, 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP).&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/v-p9LPbXglo" height="1" width="1"/&gt;</description><a10:updated>2013-04-08T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoji Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wenxiang Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huali Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Junfei Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhengbiao Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiulin Zhu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00255A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00237C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00237C</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/PURMT5l-4bg/C3PY00237C</link><title>An efficient approach to prepare ether and amide-based self-catalyzed phthalonitrile resins</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00237C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00237C, Paper&lt;/div&gt;&lt;div&gt;Amir Badshah, Michael R. Kessler, Zhou Heng, Javid Hussain Zaidi, Shahid Hameed, Aurangzeb Hasan&lt;br/&gt;Some new auto-catalyzing phthalonitrile monomers were synthesized with ether and amide linkages, which are superior compared to conventional binary non-catalyzed phthalonitrile monomers.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/PURMT5l-4bg" height="1" width="1"/&gt;</description><a10:updated>2013-03-21T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Amir Badshah</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michael R. Kessler</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhou Heng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Javid Hussain Zaidi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shahid Hameed</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Aurangzeb Hasan</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00237C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00489A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00489A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/NCqCAgy_PSE/C3PY00489A</link><title>PEGylation of Fluoridated HAp:Ln3+ Nanorods for Cell Imaging</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00489A, Paper&lt;/div&gt;&lt;div&gt;Xiaoyong Zhang, Junfeng Hui, Bin Yang, Yong Yang, Daidi Fan, Meiying Liu, Lei Tao, Yen Wei&lt;br/&gt;PEGylation is a popular approach for surface functionalization of nanoparticles to achieve improved properties and better performance. Herein, we developed a facile method for surface PEGylation of hydrophobic fluoridated hydroxyapatite...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/NCqCAgy_PSE" height="1" width="1"/&gt;</description><a10:updated>2013-05-07T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoyong Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Junfeng Hui</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bin Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yong Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Daidi Fan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Meiying Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lei Tao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yen Wei</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00489A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00431G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00431G</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/V7R6xU6zeBQ/C3PY00431G</link><title>Determination of copolymerisation characteristics in the N-carboxy anhydride polymerisation of two amino acids</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00431G, Paper&lt;/div&gt;&lt;div&gt;Mischa Zelzer, Andreas Heise&lt;br/&gt;Polypeptides are increasingly used as components for biomedical materials. Based on the variety of functional groups and the inherent biocompatibility presented by natural amino acids, the potential functionality offered by...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/V7R6xU6zeBQ" height="1" width="1"/&gt;</description><a10:updated>2013-05-07T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Mischa Zelzer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andreas Heise</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00431G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00434A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00434A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/85nP2dIpc7c/C3PY00434A</link><title>Dual pH and temperature responsive helical copolymer libraries with pendant chiral leucine moieties</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00434A, Paper&lt;/div&gt;&lt;div&gt;Kamal Bauri, Shashank Pant, Saswati Ghosh Roy, Priyadarsi De&lt;br/&gt;Reversible addition-fragmentation chain transfer (RAFT) polymerization was employed to afford two different chiral copolymer series having opposite chiroptical properties, based on 2-(2-methoxyethoxy)ethyl methacrylate (MEO2MA) and Boc-L/D-leucine methacryloyloxyethyl ester (Boc-L/D-Leu-HEMA) with...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/85nP2dIpc7c" height="1" width="1"/&gt;</description><a10:updated>2013-05-07T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Kamal Bauri</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shashank Pant</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Saswati Ghosh Roy</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Priyadarsi De</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00434A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00406F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00406F</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/pm8aSMksIoA/C3PY00406F</link><title>Novel Oxidation Responsive Mono-Cleavable Amphiphilic Di-block Polymer Micelles Labeled with Single Diselenide</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00406F, Paper&lt;/div&gt;&lt;div&gt;Tongbing Sun, Yong Jin, Rui Qi, Shaojun Peng, Baozhu Fan&lt;br/&gt;A novel diselenide-containing mono-cleavable amphiphilic di-block polymer, noted as MPEG-IPDI-SeSe-IPDI-PPG, composed with one hydrophilic poly(ethylene glycol) monomethylether (MPEG) block and one hydrophobic polypropylene glycol (PPG)block was synthesized via four coupling...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/pm8aSMksIoA" height="1" width="1"/&gt;</description><a10:updated>2013-05-07T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Tongbing Sun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yong Jin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rui Qi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shaojun Peng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Baozhu Fan</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00406F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00372H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00372H</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/RM5jp-aImmo/C3PY00372H</link><title>Push-Pull (Thio)barbituric Acid Derivatives in Dye Photosensitized Radical and Cationic Polymerization Reactions Under 457/473 nm Laser Beams or Blue LEDs.</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00372H, Paper&lt;/div&gt;&lt;div&gt;Jacques Lalevee, Mohamad Tehfe, Jean-Pierre Fouassier, Fabrice Morlet-Savary, Didier Gigmes, Bernadette Graff, Dumur Frederic&lt;br/&gt;A series of new dyes based on (thio)barbituric acid derivatives were synthesized and used as photoinitiators of polymerization upon very soft irradiations (laser diodes at 457 nm and 473 nm;...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/RM5jp-aImmo" height="1" width="1"/&gt;</description><a10:updated>2013-05-07T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jacques Lalevee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mohamad Tehfe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jean-Pierre Fouassier</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fabrice Morlet-Savary</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Didier Gigmes</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bernadette Graff</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dumur Frederic</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00372H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00252G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00252G</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/dxU4GY4MUhE/C3PY00252G</link><title>Acid and reduction dually cleavable amphiphilic comb-like copolymer micelles for controlled drug delivery</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00252G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3398-3410&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00252G, Paper&lt;/div&gt;&lt;div&gt;Wei Shao, Ke Miao, Huanhuan Liu, Chunnuan Ye, Jianzhong Du, Youliang Zhao&lt;br/&gt;Acid and reduction cleavable comb-like poly(PEG-&lt;em&gt;co&lt;/em&gt;-PCL) copolymers were synthesized and efficiently used as smart nanocarriers for stimuli-triggered release of DOX.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/dxU4GY4MUhE" height="1" width="1"/&gt;</description><a10:updated>2013-04-17T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Wei Shao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ke Miao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huanhuan Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chunnuan Ye</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jianzhong Du</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Youliang Zhao</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00252G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00352C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00352C</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/WqzbfIQ19ak/C3PY00352C</link><title>A simple combination of higher-oxidation-state FeX3 and phosphine or amine ligand for living radical polymerization of styrene, methacrylate, and acrylate</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00352C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00352C, Paper&lt;/div&gt;&lt;div&gt;Hiroshi Aoshima, Kotaro Satoh, Tomonari Umemura, Masami Kamigaito&lt;br/&gt;A higher-oxidation-state iron halide, FeX&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt;, induced living radical polymerization in conjunction with a halide initiator without any intentionally added reducing agents.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/WqzbfIQ19ak" height="1" width="1"/&gt;</description><a10:updated>2013-04-11T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hiroshi Aoshima</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kotaro Satoh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tomonari Umemura</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Masami Kamigaito</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00352C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00325F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00325F</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/HU_2aiAVjf4/C3PY00325F</link><title>New n-type polymer semiconductors based on naphthalene diimide and selenophene derivatives for organic field-effect transistors</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00325F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3187-3195&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00325F, Paper&lt;/div&gt;&lt;div&gt;Ye-Jin Hwang, Nishit M. Murari, Samson A. Jenekhe&lt;br/&gt;New alternating copolymers of naphthalene diimide and selenophene derivatives are found to be promising electron-transport materials. The highly crystalline polymers have a maximum electron mobility of 0.24 cm&lt;small&gt;&lt;sup&gt;2&lt;/sup&gt;&lt;/small&gt; V&lt;small&gt;&lt;sup&gt;-1&lt;/sup&gt;&lt;/small&gt; s&lt;small&gt;&lt;sup&gt;-1&lt;/sup&gt;&lt;/small&gt;.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/HU_2aiAVjf4" height="1" width="1"/&gt;</description><a10:updated>2013-04-11T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ye-Jin Hwang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nishit M. Murari</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Samson A. Jenekhe</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00325F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00347G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00347G</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/XgWk1PKlpQY/C3PY00347G</link><title>A controlled and versatile NCA polymerization method for the synthesis of polypeptides</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00347G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3182-3186&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00347G, Communication&lt;/div&gt;&lt;div&gt;Inmaculada Conejos-Sanchez, Aroa Duro-Castano, Alexander Birke, Matthias Barz, Maria J. Vicent&lt;br/&gt;A versatile and simple methodology for the preparation of well-defined polyglutamate nanocarriers is described.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/XgWk1PKlpQY" height="1" width="1"/&gt;</description><a10:updated>2013-04-08T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Inmaculada Conejos-Sanchez</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Aroa Duro-Castano</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alexander Birke</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Matthias Barz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Maria J. Vicent</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00347G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00110E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00110E</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/VsocM5b4iQU/C3PY00110E</link><title>Nucleophilic thiol-Michael chemistry and hyperbranched (co)polymers: synthesis and ring-opening metathesis (co)polymerization of novel difunctional exo-7-oxanorbornenes with in situ inimer formation</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00110E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3300-3311&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00110E, Paper&lt;/div&gt;&lt;div&gt;Meina Liu, Beng Hoon Tan, Robert P. Burford, Andrew B. Lowe&lt;br/&gt;Novel hyperbranched (co)polymers are prepared &lt;em&gt;via&lt;/em&gt; the direct ROMP of novel difunctional &lt;em&gt;exo&lt;/em&gt;-7-oxanorbornenes.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/VsocM5b4iQU" height="1" width="1"/&gt;</description><a10:updated>2013-04-08T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Meina Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Beng Hoon Tan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Robert P. Burford</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrew B. Lowe</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00110E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00217A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00217A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/scB5LTqS5uw/C3PY00217A</link><title>Synthesis and versatile postpolymerization modification of couplable A(BC)mD heterografted comblike block quaterpolymers</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00217A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3272-3281&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00217A, Paper&lt;/div&gt;&lt;div&gt;Xiao Jiang, Wei Shao, Kun Jiang, Meijing Zhang, Huanhuan Liu, Chunnuan Ye, Youliang Zhao&lt;br/&gt;RAFT-synthesized comblike block quaterpolymers were efficiently used as building blocks to generate four types of novel architectures &lt;em&gt;via&lt;/em&gt; postpolymerization modification.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/scB5LTqS5uw" height="1" width="1"/&gt;</description><a10:updated>2013-04-05T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xiao Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wei Shao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kun Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Meijing Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huanhuan Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chunnuan Ye</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Youliang Zhao</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00217A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00315A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00315A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/RA0r2EIvvs4/C3PY00315A</link><title>Synthesis and characterization of fluorinated polyionomers. Part I: polyperfluoro-sulfonylethoxy propylene vinyl ether sulfonimides containing aryl sulfonic acids</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00315A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3370-3383&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00315A, Paper&lt;/div&gt;&lt;div&gt;Anna M. Flach, Frederick E. Johnson, Israel Cabasso&lt;br/&gt;The synthesis and chemistry associated with the preparation of polysulfonimide polyionomers containing aryl sulfonic acids with high charge densities is reported.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/RA0r2EIvvs4" height="1" width="1"/&gt;</description><a10:updated>2013-04-05T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Anna M. Flach</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Frederick E. Johnson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Israel Cabasso</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00315A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00341H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00341H</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/nxpkbLjZolU/C3PY00341H</link><title>Novel isoindigo-based conjugated polymers for solar cells and field effect transistors</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00341H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00341H, Paper&lt;/div&gt;&lt;div&gt;Khalid Mahmood, Zheng-Ping Liu, Cuihong Li, Zhen Lu, Tao Fang, Xiao Liu, Jianjun Zhou, Ting Lei, Jian Pei, Zhishan Bo&lt;br/&gt;Three new isoindigo containing donor-acceptor (D-A) type conjugated polymers were synthesized by palladium catalyzed Suzuki polycondensation and used as donor materials for polymer solar cells (PSCs) and field effect transistors (FETs).&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/nxpkbLjZolU" height="1" width="1"/&gt;</description><a10:updated>2013-04-04T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Khalid Mahmood</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zheng-Ping Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cuihong Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhen Lu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tao Fang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiao Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jianjun Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ting Lei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jian Pei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhishan Bo</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00341H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00338H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00338H</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/pcnu-AMtfLI/C3PY00338H</link><title>Polymerization behaviors and polymer branching structures in ATRP of monovinyl and divinyl monomers</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00338H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3204-3211&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00338H, Paper&lt;/div&gt;&lt;div&gt;Wenyan Huang, Hongjun Yang, Xiaoqiang Xue, Bibiao Jiang, Jianhai Chen, Yang Yang, Hongting Pu, Yun Liu, Dongliang Zhang, Lizhi Kong, Guangqun Zhai&lt;br/&gt;Randomly branched chains formed from coupling-reaction between branched chains after core-formation regardless of charge transfer complex between bismaleimide and styrene.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/pcnu-AMtfLI" height="1" width="1"/&gt;</description><a10:updated>2013-04-03T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Wenyan Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hongjun Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoqiang Xue</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bibiao Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jianhai Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yang Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hongting Pu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yun Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dongliang Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lizhi Kong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guangqun Zhai</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00338H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00249G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00249G</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/qLrg44os_Ko/C3PY00249G</link><title>Folate-conjugated poly(N-(2-hydroxypropyl)methacrylamide-co-methacrylic acid) nanohydrogels with pH/redox dual-stimuli response for controlled drug release</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00249G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00249G, Paper&lt;/div&gt;&lt;div&gt;Yuan-Jia Pan, Dian Li, Sha Jin, Chuan Wei, Ke-Yi Wu, Jia Guo, Chang-Chun Wang&lt;br/&gt;A pH/redox dual-stimuli-responsive targeted drug delivery system was facilely prepared &lt;em&gt;via&lt;/em&gt; a distillation-precipitation polymerization and a subsequent folate modification.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/qLrg44os_Ko" height="1" width="1"/&gt;</description><a10:updated>2013-03-27T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yuan-Jia Pan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dian Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sha Jin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chuan Wei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ke-Yi Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jia Guo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chang-Chun Wang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00249G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00257H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00257H</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/zbrUvMy5TRY/C3PY00257H</link><title>Main-chain second-order nonlinear optical polyaryleneethynylenes containing isolation chromophores: enhanced nonlinear optical properties, improved optical transparency and stability</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00257H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3196-3203&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00257H, Paper&lt;/div&gt;&lt;div&gt;Wenbo Wu, Shaohui Xin, Zhen Xu, Cheng Ye, Jingui Qin, Zhen Li&lt;br/&gt;Isolation chromophores were introduced into main chain NLO polymers, to realize a large NLO coefficient, good optical transparency and stability simultaneously.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/zbrUvMy5TRY" height="1" width="1"/&gt;</description><a10:updated>2013-03-26T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Wenbo Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shaohui Xin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhen Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cheng Ye</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jingui Qin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhen Li</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00257H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00305A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00305A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/kENfGK8O0ww/C3PY00305A</link><title>Rate enhanced nitroxide-mediated miniemulsion polymerization: effect of nitroxide water solubility</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00305A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3256-3264&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00305A, Paper&lt;/div&gt;&lt;div&gt;Yi Guo, Mary E. Tysoe, Per B. Zetterlund&lt;br/&gt;Nitroxide-mediated radical polymerization of styrene in miniemulsion based on &lt;em&gt;in situ&lt;/em&gt; surfactant generation of potassium oleate has been conducted at 130 [degree]C for three nitroxides of vastly different water solubilities; 4-stearoyl-TEMPO, TEMPO and 4-hydroxy-TEMPO.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/kENfGK8O0ww" height="1" width="1"/&gt;</description><a10:updated>2013-03-25T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yi Guo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mary E. Tysoe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Per B. Zetterlund</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00305A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00251A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00251A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/hg2R3ewowMk/C3PY00251A</link><title>Benzotrithiophene and benzodithiophene-based polymers for efficient polymer solar cells with high open-circuit voltage</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00251A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3390-3397&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00251A, Paper&lt;/div&gt;&lt;div&gt;Guobing Zhang, Jianyu Yuan, Peng Li, Jingxuan Ma, Hongbo Lu, Longzhen Qiu, Wanli Ma&lt;br/&gt;Two conjugated polymers with high &lt;em&gt;V&lt;/em&gt;&lt;small&gt;&lt;sub&gt;oc&lt;/sub&gt;&lt;/small&gt; based on benzodithiophene (BDT) and alkyl-benzotrithiophene (&lt;strong&gt;P1&lt;/strong&gt;), or acyl-benzotrithiophene (&lt;strong&gt;P2&lt;/strong&gt;) were designed and synthesized.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/hg2R3ewowMk" height="1" width="1"/&gt;</description><a10:updated>2013-03-22T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Guobing Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jianyu Yuan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Peng Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jingxuan Ma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hongbo Lu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Longzhen Qiu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wanli Ma</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00251A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00289F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00289F</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/Lr4JysE_Ark/C3PY00289F</link><title>SET-LRP of hydrophobic and hydrophilic acrylates in trifluoroethanol</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00289F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3212-3224&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00289F, Paper&lt;/div&gt;&lt;div&gt;Shampa R. Samanta, Martin E. Levere, Virgil Percec&lt;br/&gt;Efficient disproportionation of CuBr-Me&lt;small&gt;&lt;sub&gt;6&lt;/sub&gt;&lt;/small&gt;-TREN in 2,2,2-trifluoroethanol (TFE) to produce "&lt;em&gt;nascent&lt;/em&gt;" Cu(0) and CuBr&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;-Me&lt;small&gt;&lt;sub&gt;6&lt;/sub&gt;&lt;/small&gt;-TREN indicates that this semifluorinated alcohol has the potential to be an excellent solvent for Cu(0) mediated single electron transfer-living radical polymerization (SET-LRP).&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/Lr4JysE_Ark" height="1" width="1"/&gt;</description><a10:updated>2013-03-22T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Shampa R. Samanta</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Martin E. Levere</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Virgil Percec</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00289F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00300K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00300K</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/dr62D1h6-dw/C3PY00300K</link><title>Fully bio-based poly(L-lactide)-b-poly(ricinoleic acid)-b-poly(L-lactide) triblock copolyesters: investigation of solid-state morphology and thermo-mechanical properties</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00300K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3357-3369&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00300K, Paper&lt;/div&gt;&lt;div&gt;Thomas Lebarbe, Emmanuel Ibarboure, Benoit Gadenne, Carine Alfos, Henri Cramail&lt;br/&gt;Fully bio-based poly(&lt;small&gt;L&lt;/small&gt;-lactide)-&lt;em&gt;b&lt;/em&gt;-poly(ricinoleic acid)-&lt;em&gt;b&lt;/em&gt;-poly(&lt;small&gt;L&lt;/small&gt;-lactide) triblock copolymers were synthesized by a combination of AB-type self-condensation of methyl ricinoleate and ring-opening polymerization of &lt;small&gt;L&lt;/small&gt;-lactide.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/dr62D1h6-dw" height="1" width="1"/&gt;</description><a10:updated>2013-03-21T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Thomas Lebarbe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Emmanuel Ibarboure</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Benoit Gadenne</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Carine Alfos</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Henri Cramail</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00300K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00235G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00235G</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/z_9FLkI-7iM/C3PY00235G</link><title>Fluorinated thienyl-quinoxaline-based D-[small pi]-A-type copolymer toward efficient polymer solar cells: synthesis, characterization, and photovoltaic properties</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00235G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3411-3418&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00235G, Paper&lt;/div&gt;&lt;div&gt;Hsieh-Chih Chen, Ying-Hsiao Chen, Chung-Hao Liu, Yen-Hao Hsu, Yun-Chen Chien, Wei-Ti Chuang, Chih-Yang Cheng, Chien-Liang Liu, Shang-Wei Chou, Shih-Huang Tung, Pi-Tai Chou&lt;br/&gt;A tailor-made fluorinated thienyl-quinoxaline-based copolymer for bulk heterojunction photovoltaics was explored.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/z_9FLkI-7iM" height="1" width="1"/&gt;</description><a10:updated>2013-03-20T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hsieh-Chih Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ying-Hsiao Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chung-Hao Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yen-Hao Hsu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yun-Chen Chien</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wei-Ti Chuang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chih-Yang Cheng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chien-Liang Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shang-Wei Chou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shih-Huang Tung</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pi-Tai Chou</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00235G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00168G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00168G</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/4tfj0SI7nIc/C3PY00168G</link><title>Synthesis, photophysical and photovoltaic properties of a new class of two-dimensional conjugated polymers containing donor-acceptor chromophores as pendant groups</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00168G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3333-3344&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00168G, Paper&lt;/div&gt;&lt;div&gt;Yu-Ying Lai, Yen-Ju Cheng, Chiu-Hsiang Chen, Sheng-Wen Cheng, Fong-Yi Cao, Chain-Shu Hsu&lt;br/&gt;A new class of two-dimensional conjugated copolymers with the D&lt;small&gt;&lt;sub&gt;1&lt;/sub&gt;&lt;/small&gt;-A(D&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;) repeating pattern is synthesized. Their photophysical and photovoltaic properties are investigated.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/4tfj0SI7nIc" height="1" width="1"/&gt;</description><a10:updated>2013-03-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yu-Ying Lai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yen-Ju Cheng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chiu-Hsiang Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sheng-Wen Cheng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fong-Yi Cao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chain-Shu Hsu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00168G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00152K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00152K</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/6dOp-FmDVtQ/C3PY00152K</link><title>Synthesis of chitin-graft-polystyrene via atom transfer radical polymerization initiated from a chitin macroinitiator</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00152K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3384-3389&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00152K, Paper&lt;/div&gt;&lt;div&gt;Kazuya Yamamoto, Sho Yoshida, Shozaburo Mine, Jun-ichi Kadokawa&lt;br/&gt;We prepared a chitin macroinitiator in an ionic liquid (AMIMBr), which was used for the synthesis of chitin-&lt;em&gt;graft&lt;/em&gt;-polystyrene by graft polymerization of styrene &lt;em&gt;via&lt;/em&gt; ATRP.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/6dOp-FmDVtQ" height="1" width="1"/&gt;</description><a10:updated>2013-03-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Kazuya Yamamoto</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sho Yoshida</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shozaburo Mine</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jun-ichi Kadokawa</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00152K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00258F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00258F</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/ggceUci9CV4/C3PY00258F</link><title>pH degradable dendron-functionalized poly(2-ethyl-2-oxazoline) prepared by a cascade "double-click" reaction</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00258F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3236-3244&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00258F, Paper&lt;/div&gt;&lt;div&gt;Kristian Kempe, Sebla Onbulak, Ulrich S. Schubert, Amitav Sanyal, Richard Hoogenboom&lt;br/&gt;In this study, we report on the synthesis of a dendron-functionalized poly(2-ethyl-2-oxazoline) in a one-pot cascade reaction approach and its aqueous solution behavior.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/ggceUci9CV4" height="1" width="1"/&gt;</description><a10:updated>2013-03-15T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Kristian Kempe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sebla Onbulak</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ulrich S. Schubert</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Amitav Sanyal</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Richard Hoogenboom</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00258F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00196B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00196B</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/SJpOwRBxAjI/C3PY00196B</link><title>Well-defined graft copolymers of tert-butyldimethylsilyl methacrylate and poly(dimethylsiloxane) macromonomers synthesized by RAFT polymerization</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00196B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3282-3292&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00196B, Paper&lt;/div&gt;&lt;div&gt;Marlene Lejars, Andre Margaillan, Christine Bressy&lt;br/&gt;Well-defined graft copolymers of &lt;em&gt;tert&lt;/em&gt;-butyldimethylsilyl methacrylate and poly(dimethylsiloxane) macromonomers synthesized by RAFT polymerization.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/SJpOwRBxAjI" height="1" width="1"/&gt;</description><a10:updated>2013-03-15T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Marlene Lejars</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andre Margaillan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christine Bressy</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00196B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00144J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00144J</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/FinljRfpcRg/C3PY00144J</link><title>Thermo-responsive "hairy-rod" polypeptides for smart antitumor drug delivery</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00144J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3345-3356&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00144J, Paper&lt;/div&gt;&lt;div&gt;Jianxun Ding, Li Zhao, Di Li, Chunsheng Xiao, Xiuli Zhuang, Xuesi Chen&lt;br/&gt;Thermo-responsive "hairy-rod" polypeptides were efficiently synthesized by the combination of ring-opening polymerization and "click" reaction as smart antitumor drug carriers.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/FinljRfpcRg" height="1" width="1"/&gt;</description><a10:updated>2013-03-14T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jianxun Ding</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Li Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Di Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chunsheng Xiao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiuli Zhuang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xuesi Chen</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00144J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00141E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00141E</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/vPk8h-SVqak/C3PY00141E</link><title>Intracellular pH-sensitive supramolecular amphiphiles based on host-guest recognition between benzimidazole and [small beta]-cyclodextrin as potential drug delivery vehicles</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00141E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3265-3271&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00141E, Paper&lt;/div&gt;&lt;div&gt;Zhe Zhang, Jianxun Ding, Xiaofei Chen, Chunsheng Xiao, Chaoliang He, Xiuli Zhuang, Li Chen, Xuesi Chen&lt;br/&gt;Intracellular pH-sensitive supramolecular block amphiphiles were designed and used for effective intracellular anticancer drug delivery.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/vPk8h-SVqak" height="1" width="1"/&gt;</description><a10:updated>2013-03-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Zhe Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jianxun Ding</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaofei Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chunsheng Xiao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chaoliang He</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiuli Zhuang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Li Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xuesi Chen</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00141E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00216K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00216K</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/L71dmMha3BE/C3PY00216K</link><title>Amphiphilic supramolecular A(B)2A quasi-triblock copolymers</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00216K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3177-3181&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00216K, Communication&lt;/div&gt;&lt;div&gt;Ulrich Mansfeld, Andreas Winter, Martin D. Hager, Grit Festag, Stephanie Hoeppener, Ulrich S. Schubert&lt;br/&gt;A supramolecular triblock copolymer A(B)&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;A was efficiently synthesized incorporating multiple hydrogen bonding at the homojunction (B-B) and heteroleptic metal complexes at the heterojunction (A-B).&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/L71dmMha3BE" height="1" width="1"/&gt;</description><a10:updated>2013-03-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ulrich Mansfeld</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andreas Winter</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Martin D. Hager</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Grit Festag</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stephanie Hoeppener</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ulrich S. Schubert</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00216K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00186E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00186E</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/lXqQHiXiVxY/C3PY00186E</link><title>Facile synthesis of thermal-responsive P(NIPAM-S)/SiO2 hybrid hollow spheres and their controllable release properties for fragrance</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00186E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3293-3299&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00186E, Paper&lt;/div&gt;&lt;div&gt;Jing Hu, Liqin Liu, Yuyao Xie, Limin Wu&lt;br/&gt;Thermal-responsive SiO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; hybrid hollow spheres were synthesized &lt;em&gt;via&lt;/em&gt; a one-step method and used for controllable release of fragrance.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/lXqQHiXiVxY" height="1" width="1"/&gt;</description><a10:updated>2013-03-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jing Hu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Liqin Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuyao Xie</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Limin Wu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00186E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00239J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00239J</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/QlqF5mjWZsU/C3PY00239J</link><title>Hydration capabilities and structures of carbonyl and ether groups in poly(3-(2-methoxyethyl)-N-vinyl-2-pyrrolidone) film</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00239J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3323-3332&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00239J, Paper&lt;/div&gt;&lt;div&gt;Hengjie Lai, Peiyi Wu&lt;br/&gt;Structural evolution of MeOE-PVP film during moisture absorption.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/QlqF5mjWZsU" height="1" width="1"/&gt;</description><a10:updated>2013-03-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hengjie Lai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Peiyi Wu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00239J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00283G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00283G</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/bacwN94I7Pk/C3PY00283G</link><title>A self-healing supramolecular polymer gel with stimuli-responsiveness constructed by crown ether based molecular recognition</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00283G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3312-3322&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00283G, Paper&lt;/div&gt;&lt;div&gt;Xuzhou Yan, Donghua Xu, Jianzhuang Chen, Mingming Zhang, Bingjie Hu, Yihua Yu, Feihe Huang&lt;br/&gt;A stimuli-responsive and self-healing cross-linked supramolecular polymer network gel is prepared by orthogonal self-assembly of two homoditopic monomers and a metallic cross-linker.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/bacwN94I7Pk" height="1" width="1"/&gt;</description><a10:updated>2013-03-12T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xuzhou Yan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Donghua Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jianzhuang Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mingming Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bingjie Hu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yihua Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Feihe Huang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00283G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00195D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00195D</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/0APQIZVUxq8/C3PY00195D</link><title>An effect on the side chain position of D-[small pi]-A-type conjugated polymers with sp2-hybridized orbitals for organic photovoltaics</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00195D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3225-3235&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00195D, Paper&lt;/div&gt;&lt;div&gt;Kwan Wook Song, Ho Jun Song, Tae Ho Lee, Soo Won Heo, Doo Kyung Moon&lt;br/&gt;D-[small pi]-A-type conjugated polymers were synthesized by using sp&lt;small&gt;&lt;sup&gt;2&lt;/sup&gt;&lt;/small&gt;-hybridized alkylidene fluorene and photovoltaic devices were fabricated at room temperature.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/0APQIZVUxq8" height="1" width="1"/&gt;</description><a10:updated>2013-03-12T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Kwan Wook Song</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ho Jun Song</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tae Ho Lee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Soo Won Heo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Doo Kyung Moon</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00195D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00118K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00118K</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/irCX6EC79gE/C3PY00118K</link><title>Effects of "mature micelle" formation of Pluronic P123 on equilibrium between lactone and carboxylate forms of 10-hydrocamptothecin in water</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00118K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3245-3255&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00118K, Paper&lt;/div&gt;&lt;div&gt;Tianyuan Ci, Ting Li, Liang Chen, Guangtao Chang, Lin Yu, Jiandong Ding&lt;br/&gt;The equilibrium fraction of the active lactone form of the anti-tumor drug 10-hydrocamptothecin in water could be significantly enhanced after the co-assembly of the drug and polymer molecules into "mature micelles".&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/irCX6EC79gE" height="1" width="1"/&gt;</description><a10:updated>2013-03-06T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Tianyuan Ci</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ting Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Liang Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guangtao Chang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lin Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiandong Ding</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00118K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00023K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00023K</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/duMEMvLJJV0/C3PY00023K</link><title>Functionalized polymersomes for biomedical applications</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00023K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;4&lt;/b&gt;,3160-3176&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00023K, Review Article&lt;/div&gt;&lt;div&gt;Prasad V. Pawar, Shalini V. Gohil, Jay Prakash Jain, Neeraj Kumar&lt;br/&gt;Functionalized polymersomes are the latest drug carrier using polymeric vesicular architecture to achieve delivery of therapeutic agents to specific tissues/organs. This review focuses on their development along with their biomedical applications.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/duMEMvLJJV0" height="1" width="1"/&gt;</description><a10:updated>2013-02-05T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Prasad V. Pawar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shalini V. Gohil</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jay Prakash Jain</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Neeraj Kumar</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00023K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00400G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00400G</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/oXnuvHjrLU4/C3PY00400G</link><title>Synthesis of high-molecular weight block copolymers of norbornene and propylene with methyl methacrylate initiated by fluorenylamido titanium complex</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00400G, Paper&lt;/div&gt;&lt;div&gt;Ryo Tanaka, Yuushou Nakayama, Takeshi Shiono&lt;br/&gt;First synthesis of norbornene-propylene-methyl methacrylate (MMA) block terpolymer was achieved using fluorenylamide-ligated titanium complex. Unlike the other block copolymerization examples of olefins and MMA, the second MMA polymerization required additional...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/oXnuvHjrLU4" height="1" width="1"/&gt;</description><a10:updated>2013-05-03T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ryo Tanaka</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuushou Nakayama</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Takeshi Shiono</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00400G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00335C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00335C</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/mTZCGwfnOJk/C3PY00335C</link><title>Pyrroloindacenodithiophene polymers: the effect of molecular structure on OFET performance</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00335C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00335C, Paper&lt;/div&gt;&lt;div&gt;Jenny E. Donaghey, Eun-Ho Sohn, Raja Shahid Ashraf, Thomas D. Anthopoulos, Scott E. Watkins, Kigook Song, Charlotte K. Williams, Iain McCulloch&lt;br/&gt;Surface molecular structure of pyrroloindacenodithiophene polymers are probed by GIWAXD to help explain the differences in observed OFET mobilities.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/mTZCGwfnOJk" height="1" width="1"/&gt;</description><a10:updated>2013-04-26T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jenny E. Donaghey</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Eun-Ho Sohn</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Raja Shahid Ashraf</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Thomas D. Anthopoulos</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Scott E. Watkins</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kigook Song</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Charlotte K. Williams</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Iain McCulloch</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00335C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00428G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00428G</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/UIj0oybEBQQ/C3PY00428G</link><title>Photochemical thiol-yne functionalization of polypeptide scaffolds</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00428G, Paper&lt;/div&gt;&lt;div&gt;Kai-Steffen Krannig, Jin Huang, Andreas Heise, Helmut Schlaad&lt;br/&gt;Copolypeptides with propargyl side chains were functionalized with different thiols (1-thio-[small beta]-D-glucose tetraacetate, 7-mercapto-4-methylcoumarin, and methyl 3-mercaptopropionate) by initiator/catalyst-free thiol-yne photochemistry. No more than 1.5 instead of ideally 2 equivalents of...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/UIj0oybEBQQ" height="1" width="1"/&gt;</description><a10:updated>2013-05-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Kai-Steffen Krannig</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jin Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andreas Heise</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Helmut Schlaad</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00428G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00391D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00391D</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/BRFFsS658cw/C3PY00391D</link><title>Synthesis and characterization of low band gap quinoxaline based D-A copolymer and its application as donor for bulk heterojunction polymer solar cells</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00391D, Paper&lt;/div&gt;&lt;div&gt;G D. Sharma&lt;br/&gt;A new alternating copolymer P comprising of benzo [1,2-b;4,5,b'] dithiophene (BDT) derivative and 4,9-bis-( 5-bromothiophene-2-yl ) - 6,7-di- (2-ethylhexyl) - [1,2,5] thiadiazolo [3,4-g] quinoxaline (DTQx) derivative electron donating and electron...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/BRFFsS658cw" height="1" width="1"/&gt;</description><a10:updated>2013-05-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">G D. Sharma</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00391D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00290J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00290J</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/KjHVQhUEYws/C3PY00290J</link><title>Solvent Annealing Induced Phase Separation and Dewetting in PMMA/SAN Blend Films: Composition Dependence</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00290J, Paper&lt;/div&gt;&lt;div&gt;Shuangshuang Zhang, Tongfei Shi, Jichun You, Yongjin Li&lt;br/&gt;The competition between "dewetting" and "phase separation" behaviors in polymer blend films attracts significant attention. The simultaneous phase separation and dewetting in PMMA/SAN [poly(methyl methacrylate) and poly(styrene-ran-acrylonitrile)] blend ultrathin films...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/KjHVQhUEYws" height="1" width="1"/&gt;</description><a10:updated>2013-05-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Shuangshuang Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tongfei Shi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jichun You</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yongjin Li</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00290J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00462G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00462G</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/u2g20MP8rU4/C3PY00462G</link><title>Pillar[5]arene-Neutral Guest Recognition Based Supramolecular Alternating Copolymer Containing [c2]Daisy Chain and bisPillar[5]arene Units.</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00462G, Paper&lt;/div&gt;&lt;div&gt;Xiaoyang Wang, Kang Han, Jian Li, Xueshun Jia, Chunju Li&lt;br/&gt;A novel supramolecular alternating copolymer with [c2]daisy-chain dimer and macrocycle host dimer as repeating units has been fabricated. A key factor for this new assembly strategy is based on a...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/u2g20MP8rU4" height="1" width="1"/&gt;</description><a10:updated>2013-05-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoyang Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kang Han</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jian Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xueshun Jia</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chunju Li</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00462G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00368J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00368J</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/rPbDtbncWFU/C3PY00368J</link><title>Indolinic Nitroxides: Evaluation of their Potential as Universal Controlled Agent for Nitroxide Mediated Polymerization</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00368J, Paper&lt;/div&gt;&lt;div&gt;Paola Astolfi, Lucedio Greci, Pierluigi Stipa, Corrado Rizzoli, Cedric Ysacco, Marion Rollet, Laurent Autissier, Antoine Tardy, Yohann Guillaneuf, Didier Gigmes&lt;br/&gt;Indolinic nitroxides derived from the 2,2-diphenyl-3-phenylimino-2,3-dihydroindol-1-yloxyl (DPAIO) nitroxide were designed to improve the bulk polymerization of methacrylate derivatives. The corresponding alkoxyamines were prepared by reacting alkyl halide and nitroxide in...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/rPbDtbncWFU" height="1" width="1"/&gt;</description><a10:updated>2013-05-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Paola Astolfi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lucedio Greci</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pierluigi Stipa</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Corrado Rizzoli</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cedric Ysacco</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Marion Rollet</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Laurent Autissier</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Antoine Tardy</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yohann Guillaneuf</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Didier Gigmes</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00368J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00494E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00494E</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/fsxch8N_R6c/C3PY00494E</link><title>Photo-responsive linear and cross-linked supramolecular polymers based on host-guest interactions</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00494E, Paper&lt;/div&gt;&lt;div&gt;Shengyi Dong, Lingyan Gao, Jinying Li, Donghua Xu, Qizhong Zhou&lt;br/&gt;By incorporating a photochromophore, azobenzene group, into a low molecular weight heteroditopic AB-type monomer, photo-responsive linear or cross-linked supramolecular polymers were prepared. After UV irradiation, both the linear and cross-linked...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/fsxch8N_R6c" height="1" width="1"/&gt;</description><a10:updated>2013-05-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Shengyi Dong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lingyan Gao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jinying Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Donghua Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qizhong Zhou</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00494E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00461A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00461A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/Z7qEr-pX2gE/C3PY00461A</link><title>A facile method to produce PBS-PEG/CNTs nancomposites with controllable electro-induced shape memory effect</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00461A, Paper&lt;/div&gt;&lt;div&gt;Cai-Li Huang, Man-Jie He, Meng Huo, Lan Du, Cong Zhan, Cheng-Jie Fan, Ke-Ke Yang, In-Joo Chin, Yu-Zhong Wang&lt;br/&gt;A facile method to develop electro-induced shape memory polymer composites with well location- and process-controlled shape recovery performance is proposed. Poly(butylene succinate) (PBS)-poly(ethylene glycol) (PEG) multiblock copolymer (PBSEG), which has...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/Z7qEr-pX2gE" height="1" width="1"/&gt;</description><a10:updated>2013-05-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Cai-Li Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Man-Jie He</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Meng Huo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lan Du</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cong Zhan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cheng-Jie Fan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ke-Ke Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">In-Joo Chin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yu-Zhong Wang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00461A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00444A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00444A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/_gSFSw80wk4/C3PY00444A</link><title>A Nondestructive, Statistical Method for Determination of Initiation Efficiency: Dipentaerythritol-Aided Synthesis of Ternary ABC3 Miktoarm Stars using a Combined "Arm-First" and "Core-First" Approach</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00444A, Paper&lt;/div&gt;&lt;div&gt;Felix Plamper, Alexander Steinschulte, Bjoern Schulte, Natascha Drude, Michael Erberich, Christian Herbert, Jun Okuda, Martin Moller&lt;br/&gt;The preparation of miktoarm stars, based on poly(ethylene oxide) (PEO), poly(N,N-dimethylaminoethyl methacrylate) (PDMAEMA) and either poly(propylene oxide) (PPO) or poly(ethyl glycidyl ether) (PEGE), is described. Hereby, partly protected dipentaerythritol (dipentaerythritoldiacetonide)...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/_gSFSw80wk4" height="1" width="1"/&gt;</description><a10:updated>2013-05-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Felix Plamper</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alexander Steinschulte</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bjoern Schulte</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Natascha Drude</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michael Erberich</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christian Herbert</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jun Okuda</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Martin Moller</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00444A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00393K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00393K</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/i8JgyGbrX1w/C3PY00393K</link><title>Ultrafine silver nanoparticles with excellent antibacterial efficacy prepared by a handover of vesicle templating to micelle stabilization</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00393K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00393K, Communication&lt;/div&gt;&lt;div&gt;Hang Lu, Li Yu, Qiuming Liu, Jianzhong Du&lt;br/&gt;Ultrafine silver nanoparticles with excellent antibacterial efficacy are prepared by a handover of vesicle templating to micelle stabilization.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/i8JgyGbrX1w" height="1" width="1"/&gt;</description><a10:updated>2013-04-23T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hang Lu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Li Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qiuming Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jianzhong Du</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00393K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00340J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00340J</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/YGSEv_jUlRQ/C3PY00340J</link><title>D-Glucose-derived PET copolyesters with enhanced Tg</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00340J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00340J, Paper&lt;/div&gt;&lt;div&gt;Cristina Japu, Antxon Martinez de Ilarduya, Abdelilah Alla, M[a] Gracia Garcia-Martin, Juan A. Galbis, Sebastian Munoz-Guerra&lt;br/&gt;Bicyclic acetalized &lt;small&gt;D&lt;/small&gt;-glucitol (G: CH&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;OH) and dimethyl &lt;small&gt;D&lt;/small&gt;-glucarate (G: COOMe) replace ethylene glycol (circles) and dimethyl terephthalate (squares) in melt polycondensation to render sugar-based PET random copolyesters with enhanced &lt;em&gt;T&lt;/em&gt;&lt;small&gt;&lt;sub&gt;g&lt;/sub&gt;&lt;/small&gt; and a satisfactory overall pattern of behavior.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/YGSEv_jUlRQ" height="1" width="1"/&gt;</description><a10:updated>2013-04-08T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Cristina Japu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Antxon Martinez de Ilarduya</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Abdelilah Alla</creator><creator xmlns="http://purl.org/dc/elements/1.1/">M[a] Gracia Garcia-Martin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Juan A. Galbis</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sebastian Munoz-Guerra</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00340J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00227F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00227F</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/zQiXIFy5FmQ/C3PY00227F</link><title>A novel polytriazole-based organogel formed by the effects of copper ions</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00227F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00227F, Communication&lt;/div&gt;&lt;div&gt;Yujing Li, Liqiang Wan, Hao Zhou, Farong Huang, Lei Du&lt;br/&gt;The mechanism of formation of GelT is identified: copper ions complex with triazole rings to form a 3D network and enable gelling in DMF or DMSO.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/zQiXIFy5FmQ" height="1" width="1"/&gt;</description><a10:updated>2013-04-10T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yujing Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Liqiang Wan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hao Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Farong Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lei Du</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00227F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00210A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00210A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/E7BBVF4VgHk/C3PY00210A</link><title>Quaternized amino poly(glycerol-methacrylate)s for enhanced pDNA delivery</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3PY00210A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3PY00210A, Paper&lt;/div&gt;&lt;div&gt;Zhixiang Liang, Xinshi Wu, Ying-Wei Yang, Cui Li, Guolin Wu, Hui Gao&lt;br/&gt;Quaternized amino PGOHMAs were proved to be effective gene delivery systems with high transfection efficacy and low cytotoxicity.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PY/~4/E7BBVF4VgHk" height="1" width="1"/&gt;</description><a10:updated>2013-04-03T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Zhixiang Liang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xinshi Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ying-Wei Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cui Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guolin Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hui Gao</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/PY/C3PY00210A</feedburner:origLink></item></channel></rss>
