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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>Mon, 13 Feb 2012 07:04:24 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/2012/PY/C2PY00465H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00465H</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/THrPAV92mEg/C2PY00465H</link><title>Two dimensional size controlled confinement of poly(vinyl pyrrolidone) in the interlayer space of swelling clay mineral</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=C2PY00465H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00465H, Paper&lt;/div&gt;&lt;div&gt;Minoru Sohmiya, Shingo Omata, Makoto Ogawa&lt;br/&gt;The size of two dimensional interlayer nanospace of dye-polymer-clay composites was controlled by the polymer contents.&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/THrPAV92mEg" height="1" width="1"/&gt;</description><a10:updated>2012-02-10T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Minoru Sohmiya</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shingo Omata</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Makoto Ogawa</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00465H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00609J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00609J</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/nbhuRIQWawM/C2PY00609J</link><title>Preparation of jellyfish-shaped amphiphilic block-graft copolymers consisting of a poly([varepsilon]-caprolactone)-block-poly(pentafluorostyrene) ring and poly(ethylene glycol) lateral brushes</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=C2PY00609J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00609J, Paper&lt;/div&gt;&lt;div&gt;Tao Cai, Wen Jing Yang, Koon-Gee Neoh, En-Tang Kang&lt;br/&gt;Jellyfish-shaped amphiphilic block-graft copolymers with a hydrophobic ring of controllable dimensions and well-defined hydrophilic polymer brushes were synthesized.&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/nbhuRIQWawM" height="1" width="1"/&gt;</description><a10:updated>2012-02-08T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Tao Cai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wen Jing Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Koon-Gee Neoh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">En-Tang Kang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00609J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00002D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00002D</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/Rkx0IuBMXUU/C2PY00002D</link><title>Facile synthesis of novel poly([small alpha]-aminonitrile) networks through one-pot Strecker reactions</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=C2PY00002D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00002D, Communication&lt;/div&gt;&lt;div&gt;Jiacheng Wang, Yoichi Masui, Makoto Onaka&lt;br/&gt;Organic polymeric networks (OPNWs) containing the repeated structural units of [small alpha]-aminonitriles were successfully prepared for the first time in high yields &lt;i&gt;via&lt;/i&gt; the one-pot Strecker reactions of dialdehydes, di/tri-amines, and trimethylsilyl cyanide (Me&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt;SiCN) under catalyst-free conditions.&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/Rkx0IuBMXUU" height="1" width="1"/&gt;</description><a10:updated>2012-02-08T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jiacheng Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yoichi Masui</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Makoto Onaka</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00002D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00547F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00547F</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/JRrDZsSsNco/C2PY00547F</link><title>High molecular weight acrylonitrile-butadiene architectures via a combination of RAFT polymerization and orthogonal copper mediated azide-alkyne cycloaddition</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=C2PY00547F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00547F, Paper&lt;/div&gt;&lt;div&gt;Christoph J. Durr, Sebastian G. J. Emmerling, Paul Lederhose, Andreas Kaiser, Sven Brandau, Michael Klimpel, Christopher Barner-Kowollik&lt;br/&gt;Alkyne-functional nitrile butadiene rubber building blocks were employed in the copper mediated 1,3-dipolar cyclization to obtain either linear polymers or crosslinked architectures.&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/JRrDZsSsNco" height="1" width="1"/&gt;</description><a10:updated>2012-02-07T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Christoph J. Durr</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sebastian G. J. Emmerling</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Paul Lederhose</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andreas Kaiser</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sven Brandau</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michael Klimpel</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christopher Barner-Kowollik</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00547F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00544A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00544A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/mXcBwprfOEM/C2PY00544A</link><title>An improved grafting technique for producing imprinted thin film composite beads</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=C2PY00544A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00544A, Paper&lt;/div&gt;&lt;div&gt;Mahadeo R. Halhalli, Carla S. A. Aureliano, Eric Schillinger, Claudia Sulitzky, M. Magdalena Titirici, Borje Sellergren&lt;br/&gt;Based on a critical method comparison we here describe a robust method for grafting of recognitive crosslinked polymer films from porous silica beads.&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/mXcBwprfOEM" height="1" width="1"/&gt;</description><a10:updated>2012-02-06T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Mahadeo R. Halhalli</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Carla S. A. Aureliano</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Eric Schillinger</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Claudia Sulitzky</creator><creator xmlns="http://purl.org/dc/elements/1.1/">M. Magdalena Titirici</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Borje Sellergren</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00544A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00417H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00417H</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/9YPR3zGJTAo/C2PY00417H</link><title>Highly thermostable rigid-rod networks constructed from an unsymmetrical bisphthalonitrile bearing phthalazinone moieties</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=C2PY00417H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00417H, Paper&lt;/div&gt;&lt;div&gt;Guipeng Yu, Cheng Liu, Xiuping Li, Jinyan Wang, Xigao Jian, Chunyue Pan&lt;br/&gt;A highly soluble unsymmetrical phthalonitrile-functional phthalazinone is generated in an efficient pathway and results in insoluble networks with excellent thermal stability.&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/~4/9YPR3zGJTAo" height="1" width="1"/&gt;</description><a10:updated>2012-02-06T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Guipeng Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cheng Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiuping Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jinyan Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xigao Jian</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chunyue Pan</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00417H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00513A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00513A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/Zfd0mDAmJUk/C2PY00513A</link><title>Tailoring polymer architectures with macromonomer azoinitiators</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=C2PY00513A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00513A, Review&lt;/div&gt;&lt;div&gt;Ufuk Yildiz, Baki Hazer, Klaus Tauer&lt;br/&gt;This review focuses on poly(ethylene glycol) based macroinimers which can be used in aqueous and non-aqueous polymerizations to synthesize branched or hyperbranched crosslinked polymers with macroscopic or nanoscopic dimensions for potential applications in materials and bio-medical sciences.&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/Zfd0mDAmJUk" height="1" width="1"/&gt;</description><a10:updated>2012-02-06T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ufuk Yildiz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Baki Hazer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Klaus Tauer</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00513A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00605G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00605G</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/9iGXwPtka1Y/C2PY00605G</link><title>A simple microfluidic device for fabrication of double emulsion droplets and polymer microcapsules</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=C2PY00605G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00605G, Paper&lt;/div&gt;&lt;div&gt;Gabit Nurumbetov, Nicholas Ballard, Stefan A. F. Bon&lt;br/&gt;Using a simple microfluidic device that can be used easily by non-specialists we produce a range of intricate functional microcapsules.&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/~4/9iGXwPtka1Y" height="1" width="1"/&gt;</description><a10:updated>2012-02-06T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Gabit Nurumbetov</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nicholas Ballard</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stefan A. F. Bon</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00605G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00601D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00601D</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/83-hRIDttlQ/C2PY00601D</link><title>Polysaccharide-stabilized core cross-linked polymer micelle analogues</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=C2PY00601D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00601D, Paper&lt;/div&gt;&lt;div&gt;Daniel J. Krasznai, Timothy F. L. McKenna, Michael F. Cunningham, Pascale Champagne, Niels M. B. Smeets&lt;br/&gt;Hyperbranched polymers synthesized from catalytic chain transfer polymerization are used to prepare block-copolymers that resemble the architecture of a core cross-linked micelle.&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/~4/83-hRIDttlQ" height="1" width="1"/&gt;</description><a10:updated>2012-02-03T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Daniel J. Krasznai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Timothy F. L. McKenna</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michael F. Cunningham</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pascale Champagne</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Niels M. B. Smeets</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00601D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY20013A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY20013A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/R9ritg9n304/C2PY20013A</link><title>Terminal functional glycopolymers via a combination of catalytic chain transfer polymerisation (CCTP) followed by three consecutive click reactions</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=C2PY20013A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY20013A, Paper&lt;/div&gt;&lt;div&gt;Qiang Zhang, Stacy Slavin, Mathew W. Jones, Alice J. Haddleton, David M. Haddleton&lt;br/&gt;CCTP and thiol-ene and alkyne azide coupling is employed to give functional glycopolymers for biological targeting giving multi gram quantities and avoiding the need for living radical polymerisation chemistry.&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/R9ritg9n304" height="1" width="1"/&gt;</description><a10:updated>2012-02-03T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Qiang Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stacy Slavin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mathew W. Jones</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alice J. Haddleton</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David M. Haddleton</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY20013A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00565D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00565D</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/wTPhc-bfNm0/C2PY00565D</link><title>Double modular modification of thiolactone-containing polymers: towards polythiols and derived structures</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=C2PY00565D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00565D, Paper&lt;/div&gt;&lt;div&gt;Pieter Espeel, Fabienne Goethals, Milan M. Stamenovic, Lionel Petton, Filip E. Du Prez&lt;br/&gt;Narrow polydisperse poly(thiolactones) are synthesized &lt;i&gt;via&lt;/i&gt; controlled copolymerization of vinyl monomers with a thiolactone containing monomer. A double modular modification (aminolysis and thiol-X) yields well-defined, multi-functional polymers.&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/wTPhc-bfNm0" height="1" width="1"/&gt;</description><a10:updated>2012-02-03T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Pieter Espeel</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fabienne Goethals</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Milan M. Stamenovic</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lionel Petton</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Filip E. Du Prez</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00565D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00559J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00559J</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/KfghmLWPco4/C2PY00559J</link><title>Time-dependent increase in aqueous solubility caused by the gradual disruption of hydrophobic aggregation</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=C2PY00559J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00559J, Paper&lt;/div&gt;&lt;div&gt;Seo-Hyun Jung, Jungju Ryu, Daewon Sohn, Hyung-il Lee&lt;br/&gt;We report the preparation of a thermoresponsive polymer whose solubility in water can be controlled simply by time elapse. We showed that the gradual disruption of hydrophobic aggregation originated from strong [small pi]-[small pi] stacking between side chain triazole rings resulting in an increase in the cloud point.&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/KfghmLWPco4" height="1" width="1"/&gt;</description><a10:updated>2012-02-03T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Seo-Hyun Jung</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jungju Ryu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Daewon Sohn</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hyung-il Lee</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00559J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00444E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00444E</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/ob3LXVqgtUM/C2PY00444E</link><title>From one-pot stabilisation to in situ functionalisation in nitroxide mediated polymerisation: an efficient extension towards atom transfer radical polymerisation</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=C2PY00444E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00444E, Paper&lt;/div&gt;&lt;div&gt;Lionel Petton, Andres E. Ciolino, Bart Dervaux, Filip E. Du Prez&lt;br/&gt;A strategy based on the controlled addition of transfer agents during NMP is investigated for the synthesis of thermally stable polymers and bromine-functionalised polymers for ATRP.&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/ob3LXVqgtUM" height="1" width="1"/&gt;</description><a10:updated>2012-02-03T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Lionel Petton</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andres E. Ciolino</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bart Dervaux</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Filip E. Du Prez</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00444E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00582D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00582D</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/Oo3Z8fK-z04/C2PY00582D</link><title>Spectroscopic study of side-chain melting and crystallization of regioregular poly(3-dodecylthiophene)</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=C2PY00582D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00582D, Communication&lt;/div&gt;&lt;div&gt;Yan Guo, Ying Jin, Zhaohui Su&lt;br/&gt;Structural evidence of side-chain melting/crystallization in P3DDT and absence of such in P3HT.&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/Oo3Z8fK-z04" height="1" width="1"/&gt;</description><a10:updated>2012-02-03T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yan Guo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ying Jin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhaohui Su</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00582D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00584K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00584K</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/sNMnEgOMPgE/C2PY00584K</link><title>Bioactive and electroactive response of flexible polythiophene:polyester nanomembranes for tissue engineering</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=C2PY00584K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00584K, Paper&lt;/div&gt;&lt;div&gt;Maria M. Perez-Madrigal, Elaine Armelin, Luis J. del Valle, Francesc Estrany, Carlos Aleman&lt;br/&gt;Flexible, degradable and bioelectroactive nanomembranes (thickness: &amp;lt;20 nm) made of polythiophene and polyester have been used as bioactive platforms.&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/sNMnEgOMPgE" height="1" width="1"/&gt;</description><a10:updated>2012-02-01T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Maria M. Perez-Madrigal</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Elaine Armelin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Luis J. del Valle</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Francesc Estrany</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Carlos Aleman</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00584K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00528J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00528J</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/71tyK-ZbXto/C2PY00528J</link><title>Benzoxazine-based phosphinated bisphenols and their application in preparing flame-retardant, low dielectric cyanate ester thermosets</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=C2PY00528J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00528J, Paper&lt;/div&gt;&lt;div&gt;Hou Chien Chang, Hung Tse Lin, Ching Hsuan Lin&lt;br/&gt;We reveal a facile synthetic route to prepare phosphinated bisphenols by combining the nucleophilicity of DOPO and ring-opening of benzoxazines. Dicyanate ester derivatives were prepared from these bisphenols to enhance flame retardancy and reduce the dielectric properties of the dicyanate ester of bisphenol A with small penalty to the thermal properties.&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/~4/71tyK-ZbXto" height="1" width="1"/&gt;</description><a10:updated>2012-02-01T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hou Chien Chang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hung Tse Lin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ching Hsuan Lin</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00528J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00591C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00591C</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/jW4U5CDX2Lw/C2PY00591C</link><title>Imidazole-accelerated crosslinking of epoxidized natural rubber by dicarboxylic acids: a mechanistic investigation using NMR spectroscopy</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=C2PY00591C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00591C, Paper&lt;/div&gt;&lt;div&gt;Myriam Pire, Cedric Lorthioir, Evdokia K. Oikonomou, Sophie Norvez, Ilias Iliopoulos, Benoit Le Rossignol, Ludwik Leibler&lt;br/&gt;Solid-state NMR spectroscopy is used to investigate the crosslinking mechanism of epoxidized natural rubber by dicarboxylic acids.&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/jW4U5CDX2Lw" height="1" width="1"/&gt;</description><a10:updated>2012-01-31T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Myriam Pire</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cedric Lorthioir</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Evdokia K. Oikonomou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sophie Norvez</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ilias Iliopoulos</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Benoit Le Rossignol</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ludwik Leibler</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00591C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00612J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00612J</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/Q6CdLR1j4K8/C2PY00612J</link><title>Novel polymer nanocomposites from bioinspired green aqueous functionalization of BNNTs</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=C2PY00612J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00612J, Paper&lt;/div&gt;&lt;div&gt;Vijay Kumar Thakur, Jian Yan, Meng-Fang Lin, Chunyi Zhi, Dmitri Golberg, Yoshio Bando, Raymond Sim, Pooi See Lee&lt;br/&gt;We report a facile and green environment-friendly approach for aqueous functionalization of boron nitride nanotubes through the bio-inspired protein, dopamine.&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/Q6CdLR1j4K8" height="1" width="1"/&gt;</description><a10:updated>2012-01-31T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Vijay Kumar Thakur</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jian Yan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Meng-Fang Lin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chunyi Zhi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dmitri Golberg</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yoshio Bando</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Raymond Sim</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pooi See Lee</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00612J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00614F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00614F</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/L2EMY_hVg7o/C2PY00614F</link><title>A new story of cyclodextrin as a bulky pendent group causing uncommon behaviour to random copolymers in solution</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=C2PY00614F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00614F, Paper&lt;/div&gt;&lt;div&gt;Fuji Sakai, Guosong Chen, Ming Jiang&lt;br/&gt;The presence of pendent cyclodextrins leads to unique thermo-induced aggregation behavior differing from its parent PNIPAM homopolymer.&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/L2EMY_hVg7o" height="1" width="1"/&gt;</description><a10:updated>2012-01-31T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Fuji Sakai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guosong Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ming Jiang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00614F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00593J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00593J</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/GibVjeMQbxk/C2PY00593J</link><title>Ladder-type poly(benzopentalene) derivatives with tunable energy levels by "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=C2PY00593J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00593J, Paper&lt;/div&gt;&lt;div&gt;Dong Wang, Xiangke Wang, Yuzhen Zhao, Hong Gao, Yan Xing, Huai Yang&lt;br/&gt;We have successfully synthesized two types of conjugated polymers, &lt;i&gt;i.e.&lt;/i&gt;, ladder-type or AB-type poly(benzopentalene) derivative macromoleculars, by Pd-catalyzed self-polycondensation.&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/GibVjeMQbxk" height="1" width="1"/&gt;</description><a10:updated>2012-01-30T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Dong Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiangke Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuzhen Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hong Gao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yan Xing</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huai Yang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00593J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00552B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00552B</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/E_HDUsiHHtk/C2PY00552B</link><title>Poly(dopamine acrylamide)-co-poly(propargyl acrylamide)-modified titanium surfaces for 'click' functionalization</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=C2PY00552B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00552B, Paper&lt;/div&gt;&lt;div&gt;Li Qun Xu, Hua Jiang, Koon-Gee Neoh, En-Tang Kang, Guo Dong Fu&lt;br/&gt;Poly(dopamine acrylamide)-&lt;i&gt;co&lt;/i&gt;-poly(propargyl acrylamide) allows the preparation of a 'clickable' Ti platform &lt;i&gt;via&lt;/i&gt; coordination interaction of the catechol in the copolymer with the Ti surface.&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/E_HDUsiHHtk" height="1" width="1"/&gt;</description><a10:updated>2012-01-30T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Li Qun Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hua Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Koon-Gee Neoh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">En-Tang Kang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guo Dong Fu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00552B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00585A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00585A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/pHH5COhQCgc/C2PY00585A</link><title>Functional conjugated microporous polymers: from 1,3,5-benzene to 1,3,5-triazine</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=C2PY00585A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00585A, Paper&lt;/div&gt;&lt;div&gt;Shijie Ren, Robert Dawson, Andrea Laybourn, Jia-xing Jiang, Yaroslav Khimyak, Dave J. Adams, Andrew I. Cooper&lt;br/&gt;Conjugated microporous polymers (CMPs) based on electron-withdrawing 1,3,5-triazine nodes show surface areas of up to 995 m&lt;small&gt;&lt;sup&gt;2&lt;/sup&gt;&lt;/small&gt; g&lt;small&gt;&lt;sup&gt;¬1&lt;/sup&gt;&lt;/small&gt;, enhanced carbon dioxide uptakes compared to non-triazine CMPs, and optical band gaps that can be engineered by copolymerization.&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/pHH5COhQCgc" height="1" width="1"/&gt;</description><a10:updated>2012-01-30T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Shijie Ren</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Robert Dawson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrea Laybourn</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jia-xing Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yaroslav Khimyak</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dave J. Adams</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrew I. Cooper</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00585A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00449F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00449F</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/n1nr89SW1QM/C2PY00449F</link><title>Flexible polybenzoxazine thermosets with high glass transition temperatures and low surface free energies</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=C2PY00449F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00449F, Paper&lt;/div&gt;&lt;div&gt;Ching Hsuan Lin, Sheng Lung Chang, Ting Yi Shen, Yu Sin Shih, Hong Tze Lin, Chih Feng Wang&lt;br/&gt;Four main-chain type polybenzoxazine precursors were synthesized from the Mannich-type polycondensation of biphenol A, paraformaldehyde, and four typical aromatic diamines. Precursors prepared in toluene/ethanol exhibit higher purity, higher molecular weight, and lead to better thermal properties after curing.&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/n1nr89SW1QM" height="1" width="1"/&gt;</description><a10:updated>2012-01-30T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ching Hsuan Lin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sheng Lung Chang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ting Yi Shen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yu Sin Shih</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hong Tze Lin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chih Feng Wang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00449F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00558A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00558A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/1CCY6HVwfQM/C2PY00558A</link><title>Synthesis and antibacterial characterization of gemini surfactant monomers and 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=C2PY00558A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00558A, Paper&lt;/div&gt;&lt;div&gt;Yi Zhang, Mingming Ding, Lijuan Zhou, Hong Tan, Jiehua Li, Huining Xiao, Jianshu Li, James Snow&lt;br/&gt;A series of novel quaternary ammonium gemini monomers with broad-spectrum antibacterial activities could be easily copolymerized using free radical polymerization to develop novel antibacterial polymers.&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/~4/1CCY6HVwfQM" height="1" width="1"/&gt;</description><a10:updated>2012-01-30T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yi Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mingming Ding</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lijuan Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hong Tan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiehua Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huining Xiao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jianshu Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">James Snow</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00558A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00606E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00606E</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/zOVH2bV6Mds/C2PY00606E</link><title>Synthesis of low-temperature benzocyclobutene cross-linker and utilization</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=C2PY00606E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00606E, Communication&lt;/div&gt;&lt;div&gt;Julia N. Dobish, Sharon K. Hamilton, Eva Harth&lt;br/&gt;A low temperature benzocyclobutene (BCB) cross-linker was developed with a 100 [degree]C lower activation temperature as known BCB systems and an intramolecular chain cross-linked nanoparticle was prepared.&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/zOVH2bV6Mds" height="1" width="1"/&gt;</description><a10:updated>2012-01-30T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Julia N. Dobish</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sharon K. Hamilton</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Eva Harth</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00606E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00564F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00564F</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/Rc-RWy2u0Zw/C2PY00564F</link><title>Direct synthesis and aqueous solution behavior of pH-responsive, zwitterionic and three-layered branched copolymer nanoparticles</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=C2PY00564F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, &lt;b&gt;3&lt;/b&gt;,625-627&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00564F, Communication&lt;/div&gt;&lt;div&gt;Erol Hasan, Steve Furzeland, Derek Atkins, Dave J. Adams, Jonathan V. M. Weaver&lt;br/&gt;The aqueous solution behavior of pH-responsive zwitterionic copolymer nanoparticles synthesized &lt;i&gt;via&lt;/i&gt; a direct and facile branching polymerization methodology 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/Rc-RWy2u0Zw" height="1" width="1"/&gt;</description><a10:updated>2012-01-30T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Erol Hasan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Steve Furzeland</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Derek Atkins</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dave J. Adams</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jonathan V. M. Weaver</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00564F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00542E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00542E</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/cNAuCB8msTY/C2PY00542E</link><title>Enzymatic miniemulsion polymerization of styrene with a polymerizable surfactant</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=C2PY00542E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00542E, Paper&lt;/div&gt;&lt;div&gt;Michinari Kohri, Ayaka Kobayashi, Haruka Fukushima, Takashi Kojima, Tatsuo Taniguchi, Kyoichi Saito, Takayuki Nakahira&lt;br/&gt;Polymer particles were prepared using horseradish peroxidase-mediated miniemulsion polymerization with a polymerizable surfactant C&lt;small&gt;&lt;sub&gt;12&lt;/sub&gt;&lt;/small&gt;-DMAEMA.&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/cNAuCB8msTY" height="1" width="1"/&gt;</description><a10:updated>2012-01-30T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Michinari Kohri</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ayaka Kobayashi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Haruka Fukushima</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Takashi Kojima</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tatsuo Taniguchi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kyoichi Saito</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Takayuki Nakahira</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00542E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00580H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00580H</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/UpJhXBP_mtw/C2PY00580H</link><title>Electronic energy transfer in pendant MEH-PPV 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=C2PY00580H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00580H, Paper&lt;/div&gt;&lt;div&gt;Andrew J. Tilley, Ming Chen, Stephen M. Danczak, Kenneth P. Ghiggino, Jonathan M. White&lt;br/&gt;Fluorescent polymers bearing short MEH-PPV side-chains have been prepared by RAFT polymerization, showing highly efficient energy transfer between pendant chromophores.&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/UpJhXBP_mtw" height="1" width="1"/&gt;</description><a10:updated>2012-01-26T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Andrew J. Tilley</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ming Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stephen M. Danczak</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kenneth P. Ghiggino</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jonathan M. White</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00580H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00567K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00567K</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/RzDnopXCY8I/C2PY00567K</link><title>Ring-opening polymerization of cyclic esters initiated by cyclodextrins</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=C2PY00567K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00567K, Minireview&lt;/div&gt;&lt;div&gt;Yong Miao, Philippe Zinck&lt;br/&gt;This mini-review reports recent developments in the use of cyclodextrins as initiators or co-initiators for the ring-opening polymerization of cyclic esters.&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/RzDnopXCY8I" height="1" width="1"/&gt;</description><a10:updated>2012-01-26T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yong Miao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Philippe Zinck</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00567K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00590E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00590E</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/t_H7aI3B9Ro/C2PY00590E</link><title>2-[1-(2,4-Dibenzhydryl-6-methylphenylimino)ethyl]-6-[1-(arylimino)ethyl]pyridylcobalt(II) dichlorides: Synthesis, characterization and ethylene polymerization 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=C2PY00590E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, &lt;b&gt;3&lt;/b&gt;,787-793&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00590E, Paper&lt;/div&gt;&lt;div&gt;Jingjuan Lai, Weizhen Zhao, Wenhong Yang, Carl Redshaw, Tongling Liang, Yongwen Liu, Wen-Hua Sun&lt;br/&gt;Cobalt(&lt;small&gt;II&lt;/small&gt;) dichlorides bearing 2-[1-(2,4-dibenzhydryl-6-methylphenylimino)ethyl]-6-[1-(arylimino)ethyl]pyridines exhibited high activities ([less-than-or-equal]1.81 [times] 10&lt;small&gt;&lt;sup&gt;7&lt;/sup&gt;&lt;/small&gt; g PE mol&lt;small&gt;&lt;sup&gt;-1&lt;/sup&gt;&lt;/small&gt;(Co) h&lt;small&gt;&lt;sup&gt;-1&lt;/sup&gt;&lt;/small&gt;) in ethylene polymerization using MAO or MMAO, producing polyethylenes with narrow polydispersity.&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/t_H7aI3B9Ro" height="1" width="1"/&gt;</description><a10:updated>2012-01-25T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jingjuan Lai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Weizhen Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wenhong Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Carl Redshaw</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tongling Liang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yongwen Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wen-Hua Sun</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00590E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00603K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00603K</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/hUFUgN3zJSE/C2PY00603K</link><title>Poly(butylene succinate)-poly(ethylene glycol) multiblock copolymer: Synthesis, structure, properties and shape memory 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=C2PY00603K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, &lt;b&gt;3&lt;/b&gt;,800-808&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00603K, Paper&lt;/div&gt;&lt;div&gt;Cai-Li Huang, Ling Jiao, Jing-Jing Zhang, Jian-Bing Zeng, Ke-Ke Yang, Yu-Zhong Wang&lt;br/&gt;Thermally-induced shape memory multiblock poly(ether-ester)s comprising crystallisable poly(butylene succinate) hard segments and poly(ethylene glycol) soft segments, were synthesized by polycondensation from succinic acid, 1,4-butanediol and PEG diol.&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/hUFUgN3zJSE" height="1" width="1"/&gt;</description><a10:updated>2012-01-23T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Cai-Li Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ling Jiao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jing-Jing Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jian-Bing Zeng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ke-Ke Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yu-Zhong Wang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00603K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00583B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00583B</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/5acG6NEzMcs/C2PY00583B</link><title>Biaxially extended quaterthiophene-thiophene and -selenophene conjugated polymers for optoelectronic device 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=C2PY00583B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, &lt;b&gt;3&lt;/b&gt;,767-777&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00583B, Paper&lt;/div&gt;&lt;div&gt;Hsiang-Wei Lin, Wen-Ya Lee, Chien Lu, Chih-Jung Lin, Hung-Chin Wu, Yu-Wei Lin, Byungcheol Ahn, Yecheol Rho, Moonhor Ree, Wen-Chang Chen&lt;br/&gt;Optoelectronic properties of biaxially extended conjugated quaterthiophene-heteroaromatic ring polymers are manipulated by the thiophene or selenophene ring number, resulting in variation of field effect mobility and photovoltaic efficiency.&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/~4/5acG6NEzMcs" height="1" width="1"/&gt;</description><a10:updated>2012-01-23T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hsiang-Wei Lin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wen-Ya Lee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chien Lu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chih-Jung Lin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hung-Chin Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yu-Wei Lin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Byungcheol Ahn</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yecheol Rho</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Moonhor Ree</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wen-Chang Chen</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00583B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00604A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00604A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/qRQNraOQ-eI/C2PY00604A</link><title>Polymers with molecular weight dependent LCSTs are essential for cooperative behaviour</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=C2PY00604A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, &lt;b&gt;3&lt;/b&gt;,794-799&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00604A, Paper&lt;/div&gt;&lt;div&gt;Nga Sze Ieong, Muhammad Hasan, Daniel J. Phillips, Yussif Saaka, Rachel K. O'Reilly, Matthew I. Gibson&lt;br/&gt;The transition temperatures of thermoresponsive polymers can be precisely tuned by a simple blending strategy, but only when the individual polymers show a strong relationship between molecular weight and their cloud point. The observed transition is shown to correlate exactly with that expected based on the overall weight-average molecular weight of the blend allowing for precision tuning of the transitions.&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/qRQNraOQ-eI" height="1" width="1"/&gt;</description><a10:updated>2012-01-23T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Nga Sze Ieong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Muhammad Hasan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Daniel J. Phillips</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yussif Saaka</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rachel K. O'Reilly</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Matthew I. Gibson</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00604A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00510G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00510G</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/_Mrf78HCRtY/C2PY00510G</link><title>Pushing the limits of copper mediated azide-alkyne cycloaddition (CuAAC) to conjugate polymeric chains to cyclic peptides</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=C2PY00510G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00510G, Paper&lt;/div&gt;&lt;div&gt;Cheuk Ka Poon, Robert Chapman, Katrina A. Jolliffe, Sebastien Perrier&lt;br/&gt;The optimal conditions for ligating polymeric chains to a cyclic octapeptide with 100% efficiency &lt;i&gt;via&lt;/i&gt; copper(&lt;small&gt;I&lt;/small&gt;)-mediated azide-alkyne cycloaddition (CuAAC) are 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/_Mrf78HCRtY" height="1" width="1"/&gt;</description><a10:updated>2012-01-23T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Cheuk Ka Poon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Robert Chapman</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Katrina A. Jolliffe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sebastien Perrier</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00510G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00531J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00531J</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/KMD95ELrcws/C2PY00531J</link><title>Amino acid vinyl esters: a new monomer palette for degradable polycationic 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=C2PY00531J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, &lt;b&gt;3&lt;/b&gt;,741-750&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00531J, Paper&lt;/div&gt;&lt;div&gt;Glen B. Thomas, Corinne E. Lipscomb, Mahesh K. Mahanthappa&lt;br/&gt;Degradable polycationic materials with tunable backbone charge densities and variable hydrophilicities are synthesized by copolymerization of vinyl acetate and &lt;i&gt;N&lt;/i&gt;-Boc-protected amino acid &lt;i&gt;O&lt;/i&gt;-vinyl esters followed by post-synthetic deprotection under different conditions.&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/KMD95ELrcws" height="1" width="1"/&gt;</description><a10:updated>2012-01-20T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Glen B. Thomas</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Corinne E. Lipscomb</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mahesh K. Mahanthappa</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00531J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00566B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00566B</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/8PzpYMhkPT8/C2PY00566B</link><title>Synthesis of conjugated diblock copolymers: two mechanistically distinct, sequential living polymerizations using a single 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=C2PY00566B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00566B, Paper&lt;/div&gt;&lt;div&gt;Zong-Quan Wu, Jonathan D. Radcliffe, Robert J. Ono, Zheng Chen, Zicheng Li, Christopher W. Bielawski&lt;br/&gt;A method for the synthesis of rod-rod conjugated diblock copolymers that self-assemble and display microphase separation characteristics is presented.&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/~4/8PzpYMhkPT8" height="1" width="1"/&gt;</description><a10:updated>2012-01-20T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Zong-Quan Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jonathan D. Radcliffe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Robert J. Ono</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zheng Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zicheng Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christopher W. Bielawski</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00566B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00540A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00540A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/P_4YCzO1Rq4/C2PY00540A</link><title>Iron-based pre-catalyst supported on polyformamidine for C-C bond 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=C2PY00540A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, &lt;b&gt;3&lt;/b&gt;,751-756&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00540A, Paper&lt;/div&gt;&lt;div&gt;Stephan Enthaler, Sebastian Krackl, Jan Dirk Epping, Bjorn Eckhardt, Steffen M. Weidner, Anna Fischer&lt;br/&gt;In the present study the application of a recyclable heterogeneous catalyst based on iron supported on polyformamidine was demonstrated in C-C bond formation reactions.&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/P_4YCzO1Rq4" height="1" width="1"/&gt;</description><a10:updated>2012-01-20T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Stephan Enthaler</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sebastian Krackl</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jan Dirk Epping</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bjorn Eckhardt</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Steffen M. Weidner</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anna Fischer</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00540A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00570K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00570K</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/7g11sbQwXek/C2PY00570K</link><title>Design and examination of an antioxidant-containing polyphosphazene scaffold for tissue engineering</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=C2PY00570K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, &lt;b&gt;3&lt;/b&gt;,778-786&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00570K, Paper&lt;/div&gt;&lt;div&gt;Nicole L. Morozowich, Jessica L. Nichol, Ryan J. Mondschein, Harry R. Allcock&lt;br/&gt;This work describes the synthesis and characterization of novel biodegradable, photoresponsive polyphosphazenes. The polymers hydrolyze in a controllable fashion while releasing the antioxidant ferulic acid.&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/~4/7g11sbQwXek" height="1" width="1"/&gt;</description><a10:updated>2012-01-19T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Nicole L. Morozowich</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jessica L. Nichol</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ryan J. Mondschein</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Harry R. Allcock</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00570K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00545J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00545J</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/qSoCAjxGYkc/C2PY00545J</link><title>Graphite oxide as a carbocatalyst for the preparation of fullerene-reinforced polyester and polyamide nanocomposites</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=C2PY00545J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, &lt;b&gt;3&lt;/b&gt;,757-766&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00545J, Paper&lt;/div&gt;&lt;div&gt;Daniel R. Dreyer, Karalee A. Jarvis, Paulo J. Ferreira, Christopher W. Bielawski&lt;br/&gt;Graphite oxide (GO) was discovered to catalyze the ring opening polymerization of various cyclic lactones and lactams to their corresponding polyesters or polyamides.&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/qSoCAjxGYkc" height="1" width="1"/&gt;</description><a10:updated>2012-01-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Daniel R. Dreyer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Karalee A. Jarvis</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Paulo J. Ferreira</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christopher W. Bielawski</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00545J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00577H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00577H</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/gG7enTI04rE/C2PY00577H</link><title>Poly(N-isopropylacrylamide) on two-dimensional graphene oxide surfaces</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=C2PY00577H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, &lt;b&gt;3&lt;/b&gt;,621-624&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00577H, Communication&lt;/div&gt;&lt;div&gt;Junjie Qi, Weipeng Lv, Guoliang Zhang, Fengbao Zhang, Xiaobin Fan&lt;br/&gt;Poly(N-isopropylacrylamide) PNIPAM-graphene oxide hybrids were prepared to reveal the changes in structure and properties of PNIPAM on a real freestanding two-dimensional surface.&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/gG7enTI04rE" height="1" width="1"/&gt;</description><a10:updated>2012-01-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Junjie Qi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Weipeng Lv</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guoliang Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fengbao Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaobin Fan</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00577H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00546H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00546H</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/kO8cyxZXeYU/C2PY00546H</link><title>A click chemistry approach to the efficient synthesis of polyoxometalate-polymer hybrids with well-defined structures</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=C2PY00546H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, &lt;b&gt;3&lt;/b&gt;,617-620&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00546H, Communication&lt;/div&gt;&lt;div&gt;Min-Biao Hu, Nan Xia, Wei Yu, Chi Ma, Jing Tang, Zhan-Yao Hou, Ping Zheng, Wei Wang&lt;br/&gt;A click-chemistry approach was used to synthesize polyoxometalate-polymer hybrids with well-defined structures. This breakthrough will promote a development in the synthesis of various polyoxometalate-polymer hybrids and broaden their potential application.&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/kO8cyxZXeYU" height="1" width="1"/&gt;</description><a10:updated>2012-01-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Min-Biao Hu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nan Xia</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wei Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chi Ma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jing Tang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhan-Yao Hou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ping Zheng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wei Wang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00546H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00529H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00529H</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/oJgbNSsi9Dc/C2PY00529H</link><title>The scope for synthesis of macro-RAFT agents by sequential insertion of single monomer units</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=C2PY00529H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00529H, Paper&lt;/div&gt;&lt;div&gt;Shadi Houshyar, Daniel J. Keddie, Graeme Moad, Roger J. Mulder, Simon Saubern, John Tsanaktsidis&lt;br/&gt;The scope for synthesis of new macro-RAFT agents (Z-C([double bond, length as m-dash]S)S-(M)-R) by sequential insertion of monomers (M) 'one at a time' into an initial RAFT agent (Z-C([double bond, length as m-dash]S)S-R) is explored.&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/oJgbNSsi9Dc" height="1" width="1"/&gt;</description><a10:updated>2012-01-17T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Shadi Houshyar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Daniel J. Keddie</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Graeme Moad</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Roger J. Mulder</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Simon Saubern</creator><creator xmlns="http://purl.org/dc/elements/1.1/">John Tsanaktsidis</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00529H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00523A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00523A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/lKOLzPulcsg/C2PY00523A</link><title>Tuning the photovoltaic parameters of thiophene-linked donor-acceptor liquid crystalline copolymers 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=C2PY00523A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, &lt;b&gt;3&lt;/b&gt;,710-717&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00523A, Paper&lt;/div&gt;&lt;div&gt;Kai Yao, Lie Chen, Yiwang Chen, Fan Li, Xingye Ren, Hongming Wang, Yongfang Li&lt;br/&gt;The photovoltaic performance reveals the good correlation between the donor/acceptor ratios in the mainchain of the copolymers with desirable open circuit voltage. A compromise pathway towards OPV application is to balance the HOMO/LUMO energy levels, the absorption coefficient, and crystallinity of polymers.&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/lKOLzPulcsg" height="1" width="1"/&gt;</description><a10:updated>2012-01-17T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Kai Yao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lie Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yiwang Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fan Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xingye Ren</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hongming Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yongfang Li</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00523A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00554A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00554A</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/ppP2fF8dkLM/C2PY00554A</link><title>Surface-initiated ring-opening metathesis polymerisation from cellulose fibres</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=C2PY00554A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, &lt;b&gt;3&lt;/b&gt;,727-733&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00554A, Paper&lt;/div&gt;&lt;div&gt;Linn Carlsson, Eva Malmstrom, Anna Carlmark&lt;br/&gt;Herein, cellulose fibres have for the first time been grafted with norbornene utilizing surface-initiated ring-opening metathesis polymerisation (SI-ROMP).&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/ppP2fF8dkLM" height="1" width="1"/&gt;</description><a10:updated>2012-01-17T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Linn Carlsson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Eva Malmstrom</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anna Carlmark</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00554A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00520D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00520D</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/JsuuywT0rwU/C2PY00520D</link><title>Near infrared labeling of PLGA for in vivo imaging of nanoparticles</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=C2PY00520D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, &lt;b&gt;3&lt;/b&gt;,694-702&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00520D, Paper&lt;/div&gt;&lt;div&gt;Regina Reul, Nicolas Tsapis, Herve Hillaireau, Lucie Sancey, Simona Mura, Marion Recher, Julien Nicolas, Jean-Luc Coll, Elias Fattal&lt;br/&gt;PLGA was efficiently coupled with a fluorescent NIR dye and incorporated into PLGA nanoparticles with excellent &lt;i&gt;in vivo&lt;/i&gt; imaging performance.&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/JsuuywT0rwU" height="1" width="1"/&gt;</description><a10:updated>2012-01-17T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Regina Reul</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nicolas Tsapis</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Herve Hillaireau</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lucie Sancey</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Simona Mura</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Marion Recher</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Julien Nicolas</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jean-Luc Coll</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Elias Fattal</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00520D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00499B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00499B</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/x7vhWC-e4WM/C2PY00499B</link><title>Highly sensitive detection of DNA-binding proteins based on a cationic conjugated polymer via a target-mediated fluorescence resonance energy transfer (TMFRET) strategy</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=C2PY00499B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, &lt;b&gt;3&lt;/b&gt;,703-709&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00499B, Paper&lt;/div&gt;&lt;div&gt;Xingfen Liu, Lan Ouyang, Yanqin Huang, Xiaomiao Feng, Quli Fan, Wei Huang&lt;br/&gt;A novel target-mediated FRET strategy for highly sensitive, visual and quantitative detection of DNA-binding proteins by using signal-amplifying conjugated 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/x7vhWC-e4WM" height="1" width="1"/&gt;</description><a10:updated>2012-01-17T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xingfen Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lan Ouyang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yanqin Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaomiao Feng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Quli Fan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wei Huang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00499B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00563H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00563H</guid><link>http://feeds.rsc.org/~r/rss/PY/~3/IQc5vGv7Zog/C2PY00563H</link><title>From a benzodiazaborole-based compound to donor-acceptor polymer via electropolymerization</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=C2PY00563H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2012, &lt;b&gt;3&lt;/b&gt;,613-616&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PY00563H, Communication&lt;/div&gt;&lt;div&gt;Shotaro Hayashi, Toshio Koizumi&lt;br/&gt;A benzodiazaborole-based conjugated polymer was successfully synthesized by electropolymerization. This new material exhibited charge transfer interaction and an extended conjugated system derived from the existence of borole moiety.&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/IQc5vGv7Zog" height="1" width="1"/&gt;</description><a10:updated>2012-01-16T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Shotaro Hayashi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Toshio Koizumi</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PY/C2PY00563H</feedburner:origLink></item></channel></rss>

