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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 - New J. Chem. latest articles</title><link>http://pubs.rsc.org/en/Journals/Journal/NJ</link><description>RSC - New J. Chem. latest articles</description><copyright>Copyright (c)  The Royal Society of Chemistry</copyright><lastBuildDate>Sat, 25 May 2013 00:45:52 Z</lastBuildDate><category>RSC - New J. Chem. latest articles</category><image><url>http://pubs.rsc.org/content/NewImages/rsc_publishing_logo.gif</url><title>RSC - New J. Chem. latest articles</title><link>http://pubs.rsc.org/en/Journals/Journal/NJ</link></image><atom10:link xmlns:atom10="http://www.w3.org/2005/Atom" rel="self" type="application/rss+xml" href="http://feeds.rsc.org/rss/NJ" /><feedburner:info uri="rss/nj" /><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/NJ/C3NJ00227F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00227F</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/JQUy7vhTSXA/C3NJ00227F</link><title>Electrochemical synthesis and structural characterization of homoleptic and heteroleptic cobalt, nickel, copper, zinc and cadmium compounds with the 2-hydroxy-1,4-naphthoquinone ligand</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=C3NJ00227F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00227F, Paper&lt;/div&gt;&lt;div&gt;Isabel Casanova, Antonio Sousa-Pedrares, Joaquin Viqueira, Maria L. Duran, Jaime Romero, Antonio Sousa, Jose A. Garcia-Vazquez&lt;br/&gt;One-pot electrochemical synthesis of metal complexes containing 2-hydroxy-1,4-naphthoquinone is reported.&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/NJ/~4/JQUy7vhTSXA" 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/">Isabel Casanova</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Antonio Sousa-Pedrares</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Joaquin Viqueira</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Maria L. Duran</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jaime Romero</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Antonio Sousa</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jose A. Garcia-Vazquez</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00227F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00135K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00135K</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/kHNTmP6GEWk/C3NJ00135K</link><title>Green synthesis of silver nanowires via ultraviolet irradiation catalyzed by phosphomolybdic acid and their antibacterial 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=C3NJ00135K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00135K, Paper&lt;/div&gt;&lt;div&gt;Lanlan Liu, Chaodong He, Jia Li, Jinbao Guo, Dian Yang, Jie Wei&lt;br/&gt;Silver nanowires with high aspect ratios have been synthesized by a "green chemistry-type" reaction &lt;em&gt;via&lt;/em&gt; ultraviolet irradiation in the presence of phosphomolybdic acid and show good antibacterial activity.&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/NJ/~4/kHNTmP6GEWk" 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/">Lanlan Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chaodong He</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jia Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jinbao Guo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dian Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jie Wei</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00135K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ40897C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ40897C</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/XkSxoHbv-cI/C3NJ40897C</link><title>Colorimetric detection of glutathione in human blood serum based on the reduction of oxidized TMB</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=C3NJ40897C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ40897C, Paper&lt;/div&gt;&lt;div&gt;Xing Liu, Qi Wang, Yu Zhang, Lichun Zhang, Yingying Su, Yi Lv&lt;br/&gt;Colorimetric detection of glutathione based on the catalytic reduction of oxidized TMB.&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/NJ/~4/XkSxoHbv-cI" height="1" width="1"/&gt;</description><a10:updated>2013-04-18T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xing Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qi Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yu Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lichun Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yingying Su</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yi Lv</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ40897C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00300K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00300K</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/QcfHdJO00Ms/C3NJ00300K</link><title>Dendrimers as macromolecular tools to tackle from colon to brain tumor types: a concise overview</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00300K, Perspective&lt;/div&gt;&lt;div&gt;Jean-Pierre Majoral, Serge Mignani&lt;br/&gt;It is well documented that dendrimers were described as one of the most tunable nanomaterials both for therapeutic applications and diagnostics. This concise review surveys the different types of both...&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/NJ/~4/QcfHdJO00Ms" height="1" width="1"/&gt;</description><a10:updated>2013-05-22T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jean-Pierre Majoral</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Serge Mignani</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00300K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00196B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00196B</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/iINPTY-QspE/C3NJ00196B</link><title>Structural and spin diversity of M(indenyl)2 transition-metal complexes: a DFT investigation</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=C3NJ00196B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00196B, Paper&lt;/div&gt;&lt;div&gt;Faiza Chekkal, Saber-Mustapha Zendaoui, Bachir Zouchoune, Jean-Yves Saillard&lt;br/&gt;The indenyl ligand can coordinate through its six-membered ring and, in contrast to cyclopentadienyl, allow low-lying high-spin states.&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/NJ/~4/iINPTY-QspE" height="1" width="1"/&gt;</description><a10:updated>2013-05-20T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Faiza Chekkal</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Saber-Mustapha Zendaoui</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bachir Zouchoune</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jean-Yves Saillard</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00196B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41086B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41086B</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/BnE9Bzn_aGQ/C3NJ41086B</link><title>Photo-induced electron transfer in a pyrenylcarbazole containing polymer-multiwalled carbon nanotube composite</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=C3NJ41086B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1833-1842&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ41086B, Paper&lt;/div&gt;&lt;div&gt;Lihong Yu, Kin Cheung Lo, Jingyu Xi, David Lee Phillips, Wai Kin Chan&lt;br/&gt;A very rapid photo-induced electron transfer process was observed between a pyrenylcarbazole containing polymer and a multiwalled carbon nanotube.&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/NJ/~4/BnE9Bzn_aGQ" 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/">Lihong Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kin Cheung Lo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jingyu Xi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David Lee Phillips</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wai Kin Chan</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41086B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ90017G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ90017G</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/pREETTirgLo/C3NJ90017G</link><title>Chemistry in China</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=C3NJ90017G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1644-1644&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ90017G, Editorial&lt;/div&gt;&lt;div&gt;&lt;br/&gt;This themed issue arises from the 2012 &lt;em&gt;NJC&lt;/em&gt; Symposium Series on New Directions in Chemistry held in Hong Kong, Shanghai and Beijing.&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/NJ/~4/pREETTirgLo" height="1" width="1"/&gt;</description><a10:updated>2013-05-07T00:00:00+01:00</a10:updated><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ90017G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00253E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00253E</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/pnOdAwPTVXU/C3NJ00253E</link><title>Lectin-carbohydrate interactions on nanoporous gold monoliths</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=C3NJ00253E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00253E, Paper&lt;/div&gt;&lt;div&gt;Yih Horng Tan, Kohki Fujikawa, Papapida Pornsuriyasak, Allan J. Alla, N. Vijaya Ganesh, Alexei V. Demchenko, Keith J. Stine&lt;br/&gt;Free-standing monolithic structures of nanoporous gold can be carbohydrate modified and used for capture and release of lectins.&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/NJ/~4/pnOdAwPTVXU" height="1" width="1"/&gt;</description><a10:updated>2013-05-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yih Horng Tan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kohki Fujikawa</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Papapida Pornsuriyasak</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Allan J. Alla</creator><creator xmlns="http://purl.org/dc/elements/1.1/">N. Vijaya Ganesh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alexei V. Demchenko</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Keith J. Stine</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00253E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00121K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00121K</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/WLaBWXcszFk/C3NJ00121K</link><title>Syntheses, photophysical, electroluminescence and computational studies of rhenium(I) diimine triarylamine-containing alkynyl complexes</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=C3NJ00121K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1753-1767&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00121K, Paper&lt;/div&gt;&lt;div&gt;Wai-Kin Chung, Keith Man-Chung Wong, Wai Han Lam, Xiuling Zhu, Nianyong Zhu, Hoi-Sing Kwok, Vivian Wing-Wah Yam&lt;br/&gt;The synthesis, electrochemical, photophysical, photochemical, electroluminescence and computational studies of a series of triarylamine-containing rhenium(&lt;small&gt;I&lt;/small&gt;) diimine alkynyl complexes have been 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/NJ/~4/WLaBWXcszFk" height="1" width="1"/&gt;</description><a10:updated>2013-04-29T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Wai-Kin Chung</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Keith Man-Chung Wong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wai Han Lam</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiuling Zhu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nianyong Zhu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hoi-Sing Kwok</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Vivian Wing-Wah Yam</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00121K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00062A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00062A</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/srfLVDgawAQ/C3NJ00062A</link><title>Effects of substituents on the formation of rhenium carbyne and [small eta]2-vinyl complexes from the reactions of ReH5(PMe2Ph)3 with terminal alkynes</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=C3NJ00062A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1823-1832&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00062A, Paper&lt;/div&gt;&lt;div&gt;Guomei He, Ting Fan, Jiangxi Chen, Herman Ho-Yung Sung, Ian Duncan Williams, Zhenyang Lin, Guochen Jia&lt;br/&gt;Reactions of ReH&lt;small&gt;&lt;sub&gt;5&lt;/sub&gt;&lt;/small&gt;(PMe&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;Ph)&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt; with alkynes HC[triple bond, length as m-dash]CR in the presence of HCl produce the carbyne complexes Re([triple bond, length as m-dash]CCH&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;R)Cl&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;(PMe&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;Ph)&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt; and/or the [small eta]&lt;small&gt;&lt;sup&gt;2&lt;/sup&gt;&lt;/small&gt;-vinyl complexes Re([small eta]&lt;small&gt;&lt;sup&gt;2&lt;/sup&gt;&lt;/small&gt;-CH&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;CR)Cl&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;(PMe&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;Ph)&lt;small&gt;&lt;sub&gt;3&lt;/sub&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/NJ/~4/srfLVDgawAQ" 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/">Guomei He</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ting Fan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiangxi Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Herman Ho-Yung Sung</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ian Duncan Williams</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhenyang Lin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guochen Jia</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00062A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00116D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00116D</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/JIIqaW9qaJw/C3NJ00116D</link><title>A new perylene bisimide bola amphiphile: synthesis, characterization, fluorescent properties and applications as a potential probe</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=C3NJ00116D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00116D, Paper&lt;/div&gt;&lt;div&gt;Marco Franceschin, Cecilia Bombelli, Silvia Borioni, Giuseppina Bozzuto, Silvia Eleuteri, Giovanna Mancini, Agnese Molinari, Armandodoriano Bianco&lt;br/&gt;A new bisimidic perylene bola amphiphile could be used as an aspecific vital stain for lipids of membranes, and, entrapped in specific liposomes, to label specific cell subcompartments.&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/NJ/~4/JIIqaW9qaJw" 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/">Marco Franceschin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cecilia Bombelli</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Silvia Borioni</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Giuseppina Bozzuto</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Silvia Eleuteri</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Giovanna Mancini</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Agnese Molinari</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Armandodoriano Bianco</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00116D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00031A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00031A</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/ne-cyaQlCIU/C3NJ00031A</link><title>Different salt derivatives of phenanthroindolizidine alkaloids display different in vitro antitumor activity</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=C3NJ00031A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1817-1822&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00031A, Paper&lt;/div&gt;&lt;div&gt;Meng Wu, Zi-Wen Wang, Yu-Xiu Liu, Hai-Bin Song, Ao Zhang, Ling-Hua Meng, Qing-Min Wang&lt;br/&gt;The salt derivatives of (&lt;em&gt;S&lt;/em&gt;)-6-&lt;em&gt;O&lt;/em&gt;-desmethylantofine and tylophorine were prepared and systematically evaluated for their antitumor activity. (&lt;em&gt;S&lt;/em&gt;)-6-&lt;em&gt;O&lt;/em&gt;-Desmethylantofine hydroiodide with a low nanomolar level of antitumor activity emerged as a new lead.&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/NJ/~4/ne-cyaQlCIU" 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/">Meng Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zi-Wen Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yu-Xiu Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hai-Bin Song</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ao Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ling-Hua Meng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qing-Min Wang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00031A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00032J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00032J</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/-GL74aOAsbI/C3NJ00032J</link><title>Design, synthesis and acaricidal/insecticidal activities of etoxazole 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=C3NJ00032J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1803-1810&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00032J, Paper&lt;/div&gt;&lt;div&gt;Yu-xiu Liu, Xing-cun Wei, Yong-qiang Li, Na Yang, Qing-min Wang&lt;br/&gt;Based on the structure-activity relationship of etoxazole analogues and benzoylphenylureas, a series of 2-(2,6-difluorophenyl)-4-(4-substitutedphenyl)-1,3-oxazolines &lt;strong&gt;4a-y&lt;/strong&gt; were designed and synthesized, and found to have excellent acaricidal and insecticidal activity.&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/NJ/~4/-GL74aOAsbI" 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/">Yu-xiu Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xing-cun Wei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yong-qiang Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Na Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qing-min Wang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00032J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00102D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00102D</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/QYlDt_ax-O0/C3NJ00102D</link><title>Ruthenium-catalyzed oxidation of alcohols by bromate 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=C3NJ00102D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1707-1710&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00102D, Letter&lt;/div&gt;&lt;div&gt;Zongmin Hu, Li Ma, Jianhui Xie, Hongxia Du, William W. Y. Lam, Tai-Chu Lau&lt;br/&gt;&lt;em&gt;cis&lt;/em&gt;-[Ru(2,9-Me&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;phen)&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;(OH&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;]&lt;small&gt;&lt;sup&gt;2+&lt;/sup&gt;&lt;/small&gt; is a highly efficient catalyst for the oxidation of alcohols in water using sodium bromate (NaBrO&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt;) as the terminal oxidant, with a turnover number &amp;gt;1.7 [times] 10&lt;small&gt;&lt;sup&gt;5&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/NJ/~4/QYlDt_ax-O0" 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/">Zongmin Hu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Li Ma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jianhui Xie</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hongxia Du</creator><creator xmlns="http://purl.org/dc/elements/1.1/">William W. Y. Lam</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tai-Chu Lau</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00102D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00170A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00170A</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/g-KZn58AHvU/C3NJ00170A</link><title>Small-molecular blue phosphorescent dyes for organic light-emitting devices</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=C3NJ00170A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1665-1683&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00170A, Perspective&lt;/div&gt;&lt;div&gt;Cheuk-Lam Ho, Wai-Yeung Wong&lt;br/&gt;An overview of the recent progress in the molecular design, synthesis and OLED application of small-molecule blue phosphorescent dopants is presented in this perspective article.&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/NJ/~4/g-KZn58AHvU" 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/">Cheuk-Lam Ho</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wai-Yeung Wong</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00170A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00150D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00150D</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/YgWVoHZEl7Y/C3NJ00150D</link><title>Electronic structures and binding properties of chalcogenolate-bridged molecular wheels of ruthenium and osmium</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=C3NJ00150D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1811-1816&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00150D, Paper&lt;/div&gt;&lt;div&gt;YuHe Kan, Ken Chi-Hang Tso, Sharon Lai-Fung Chan, Xiangguo Guan, Chi-Ming Che&lt;br/&gt;This present work describes the theoretical study on the formation, optical, electronic and binding properties of molecular wheels [M(ER)&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;(CO)&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;]&lt;small&gt;&lt;sub&gt;&lt;em&gt;n&lt;/em&gt;&lt;/sub&gt;&lt;/small&gt; (M = Ru or Os, E = S or Se, R = alkyl or aryl group, &lt;em&gt;n&lt;/em&gt; = 6 or 8) using DFT calculations.&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/NJ/~4/YgWVoHZEl7Y" height="1" width="1"/&gt;</description><a10:updated>2013-04-16T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">YuHe Kan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ken Chi-Hang Tso</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sharon Lai-Fung Chan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiangguo Guan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chi-Ming Che</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00150D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00065F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00065F</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/7Zjj2JjRdJE/C3NJ00065F</link><title>Preparation and photodynamic therapy application of NaYF4:Yb, Tm-NaYF4:Yb, Er multifunctional upconverting 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=C3NJ00065F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1782-1788&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00065F, Paper&lt;/div&gt;&lt;div&gt;Xiaolan Chen, Zengxia Zhao, Mengying Jiang, Daiping Que, Saige Shi, Nanfeng Zheng&lt;br/&gt;Photosensitizer loaded core-shell NaYF&lt;small&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;/small&gt;:Yb&lt;small&gt;&lt;sup&gt;3+&lt;/sup&gt;&lt;/small&gt;, Tm&lt;small&gt;&lt;sup&gt;3+&lt;/sup&gt;&lt;/small&gt;-NaYF&lt;small&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;/small&gt;:Yb&lt;small&gt;&lt;sup&gt;3+&lt;/sup&gt;&lt;/small&gt;, Er&lt;small&gt;&lt;sup&gt;3+&lt;/sup&gt;&lt;/small&gt; upconversion nanoparticles (UCNP@PEG-phospholipid/chlorin e6) were prepared and applied in photodynamic therapy.&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/NJ/~4/7Zjj2JjRdJE" 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/">Xiaolan Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zengxia Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mengying Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Daiping Que</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Saige Shi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nanfeng Zheng</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00065F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00188A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00188A</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/1viszehIjJQ/C3NJ00188A</link><title>Well-graphitized graphene as photoinduced charge transport channel for improving the photocatalytic activity of AgBr</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=C3NJ00188A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1797-1802&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00188A, Paper&lt;/div&gt;&lt;div&gt;Junfei Liang, Hua Wang, Lidong Li, Yue Xu, Lin Guo&lt;br/&gt;AgBr-well-graphitized graphene nanocomposites were prepared for the first time and the as-prepared nanocomposites exhibit extraordinary photocatalytic properties for the degradation of organic pollutants.&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/NJ/~4/1viszehIjJQ" 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/">Junfei Liang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hua Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lidong Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yue Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lin Guo</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00188A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00095H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00095H</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/h0CqlVKk8mE/C3NJ00095H</link><title>Transition-metal-free cross-dehydrogenative alkylation of pyridines under neutral conditions</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=C3NJ00095H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1704-1706&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00095H, Letter&lt;/div&gt;&lt;div&gt;Xin Li, Hao-Yuan Wang, Zhang-Jie Shi&lt;br/&gt;A mild and transition-metal-free method has been developed for the direct dehydrogenative coupling of unprotonated pyridine derivatives and a series of coupling partners such as 1,4-dioxane, THF, DME, toluene &lt;em&gt;etc&lt;/em&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/NJ/~4/h0CqlVKk8mE" 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/">Xin Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hao-Yuan Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhang-Jie Shi</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00095H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00261F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00261F</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/0lU1cnLAIOQ/C3NJ00261F</link><title>Preparation of nitrogen-containing mesoporous carbons and their application in supercapacitors</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=C3NJ00261F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1768-1775&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00261F, Paper&lt;/div&gt;&lt;div&gt;Yanfang Song, Dandan Zhou, Yonggang Wang, Congxiao Wang, Yongyao Xia&lt;br/&gt;The ordered nitrogen-containing mesoporous carbons prepared from quinoline-polymerized pitch exhibit a high capacitance of up to 290 F g&lt;small&gt;&lt;sup&gt;-1&lt;/sup&gt;&lt;/small&gt; in 1 mol L&lt;small&gt;&lt;sup&gt;-1&lt;/sup&gt;&lt;/small&gt; H&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;SO&lt;small&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;/small&gt; aqueous electrolytes due to the co-contribution of double layer capacitance and pseudo capacitance and to the unique pore structure and nitrogen functionalities.&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/NJ/~4/0lU1cnLAIOQ" 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/">Yanfang Song</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dandan Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yonggang Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Congxiao Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yongyao Xia</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00261F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00048F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00048F</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/jdWQXwaI20o/C3NJ00048F</link><title>The self-assembly effect in NLO polymers containing isolation chromophores: enhanced NLO coefficient 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=C3NJ00048F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1789-1796&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00048F, Paper&lt;/div&gt;&lt;div&gt;Wenbo Wu, Zhen Xu, Ying Xiong, Shaohui Xin, Hongding Tang, Cheng Ye, Guofu Qiu, Jingui Qin, Zhen Li&lt;br/&gt;An Ar-Ar&lt;small&gt;&lt;sup&gt;F&lt;/sup&gt;&lt;/small&gt; self-assembly effect was utilized to further improve the NLO coefficient and stability of NLO polymers containing isolation chromophores.&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/NJ/~4/jdWQXwaI20o" height="1" width="1"/&gt;</description><a10:updated>2013-04-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Wenbo Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhen Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ying Xiong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shaohui Xin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hongding Tang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cheng Ye</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guofu Qiu</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/NJ/C3NJ00048F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00050H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00050H</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/atUl8EANckk/C3NJ00050H</link><title>New core-expanded naphthalene diimides with different functional groups for air-stable solution-processed organic n-type semiconductors</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=C3NJ00050H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1720-1727&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00050H, Paper&lt;/div&gt;&lt;div&gt;Xin Chen, Jianguo Wang, Guanxin Zhang, Zitong Liu, Wei Xu, Deqing Zhang&lt;br/&gt;Four non-symmetric core-expanded NDI derivatives &lt;strong&gt;1-4&lt;/strong&gt; with low-lying LUMO energies are reported. Solution-processed OFET devices based on thin films of &lt;strong&gt;1-4&lt;/strong&gt; show n-type semiconducting behaviours.&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/NJ/~4/atUl8EANckk" height="1" width="1"/&gt;</description><a10:updated>2013-03-26T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xin Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jianguo Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guanxin Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zitong Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wei Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Deqing Zhang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00050H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00123G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00123G</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/T5fDy5pJPNM/C3NJ00123G</link><title>Large-scale assembly of semiconductor nanowires into desired patterns for sensor 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=C3NJ00123G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1776-1781&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00123G, Paper&lt;/div&gt;&lt;div&gt;Bin Zou, Xiujuan Zhang, Yan Wang, Chao Gong, Yuping Zhang, Jiansheng Jie, Wei Deng, Xiaohong Zhang&lt;br/&gt;We report a facile method to assemble silicon nanowires into large-area desired patterns by applying an external alternating electrical field between two photoresist-patterned indium tin oxide electrodes.&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/NJ/~4/T5fDy5pJPNM" height="1" width="1"/&gt;</description><a10:updated>2013-03-25T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Bin Zou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiujuan Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yan Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chao Gong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuping Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiansheng Jie</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wei Deng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaohong Zhang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00123G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00036B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00036B</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/Jz9SsH6JO3I/C3NJ00036B</link><title>Preparation and photophysical properties of a tetraethylene glycol-linked phthalocyanine-porphyrin dyad and triad</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=C3NJ00036B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1746-1752&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00036B, Paper&lt;/div&gt;&lt;div&gt;Eugeny A. Ermilov, Xuebing Leng, Beate Roder, Dennis K. P. Ng&lt;br/&gt;The captioned hetero-arrays have been prepared and studied for their photoinduced processes using various steady-state and time-resolved spectroscopic methods.&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/NJ/~4/Jz9SsH6JO3I" height="1" width="1"/&gt;</description><a10:updated>2013-03-15T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Eugeny A. Ermilov</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xuebing Leng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Beate Roder</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dennis K. P. Ng</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00036B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00063J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00063J</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/NP4JMDqP3BI/C3NJ00063J</link><title>Switching the emission of tetrakis(4-methoxyphenyl)ethylene among three colors in the solid state</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=C3NJ00063J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1696-1699&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00063J, Letter&lt;/div&gt;&lt;div&gt;Chenyu Li, Xiaoliang Luo, Weijun Zhao, Cuihong Li, Zhengping Liu, Zhishan Bo, Yuping Dong, Yong Qiang Dong, Ben Zhong Tang&lt;br/&gt;Emission of a luminogen could be switched among three colors, and its mechanochromic fluorescence affords potential applications as an optical recording material.&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/NJ/~4/NP4JMDqP3BI" height="1" width="1"/&gt;</description><a10:updated>2013-03-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Chenyu Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoliang Luo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Weijun Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cuihong Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhengping Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhishan Bo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuping Dong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yong Qiang Dong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ben Zhong Tang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00063J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41163J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41163J</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/r-UtxLt17Us/C3NJ41163J</link><title>Catalytic hydroxylation of benzene to phenol with hydrogen peroxide using catalysts based on molecular sieves</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=C3NJ41163J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1654-1664&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ41163J, Perspective&lt;/div&gt;&lt;div&gt;Tao Jiang, Weitao Wang, Buxing Han&lt;br/&gt;This perspective discusses the recent progress in the direct hydroxylation of benzene toward phenol using hydrogen peroxide as the oxidant with catalysts based on molecular sieves.&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/NJ/~4/r-UtxLt17Us" height="1" width="1"/&gt;</description><a10:updated>2013-03-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Tao Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Weitao Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Buxing Han</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41163J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00067B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00067B</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/mIM8SAHpbGg/C3NJ00067B</link><title>Direct synthesis of pyrroles via 1,3-dipolar cycloaddition of azomethine ylides with ynones</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=C3NJ00067B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1742-1745&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00067B, Paper&lt;/div&gt;&lt;div&gt;Zheng Wang, Ying Shi, Xiaoyan Luo, De-Man Han, Wei-Ping Deng&lt;br/&gt;A direct and facile synthesis of multisubstituted pyrroles &lt;em&gt;via&lt;/em&gt; AgOAc-catalyzed 1,3-dipolar cycloaddition of azomethine ylides with ynones is developed, providing the corresponding adducts in good yields (up to 89%).&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/NJ/~4/mIM8SAHpbGg" height="1" width="1"/&gt;</description><a10:updated>2013-03-08T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Zheng Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ying Shi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoyan Luo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">De-Man Han</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wei-Ping Deng</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00067B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00045A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00045A</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/uc8RzklBhCc/C3NJ00045A</link><title>Transition-metal-free aerobic oxidation of primary alcohols to carboxylic 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=C3NJ00045A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1700-1703&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00045A, Letter&lt;/div&gt;&lt;div&gt;Jing Wang, Chao Liu, Jiwen Yuan, Aiwen Lei&lt;br/&gt;A transition-metal-free aerobic oxidation of primary alcohols to acids was achieved in the presence of NaOH or &lt;small&gt;&lt;sup&gt;&lt;em&gt;t&lt;/em&gt;&lt;/sup&gt;&lt;/small&gt;BuONa. This transformation provides an effective protocol towards the synthesis of aryl, alkyl, heterocyclic and vinyl carboxylic acids.&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/NJ/~4/uc8RzklBhCc" height="1" width="1"/&gt;</description><a10:updated>2013-03-06T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jing Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chao Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiwen Yuan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Aiwen Lei</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00045A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00044C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00044C</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/yWk9kgx26sI/C3NJ00044C</link><title>Copper-mediated oxidative difluoromethylenation of aryl boronic acids with [small alpha]-silyldifluoromethylphosphonates: a new method for aryldifluorophosphonates</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=C3NJ00044C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1736-1741&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00044C, Paper&lt;/div&gt;&lt;div&gt;Xueliang Jiang, Lingling Chu, Feng-Ling Qing&lt;br/&gt;An unprecedented copper-mediated oxidative difluoromethylenation of aryl boronic acids with [small alpha]-silyldifluoromethylphosphonates has been developed, allowing rapid access to a wide range of aryldifluorophosphonates containing various functional groups.&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/NJ/~4/yWk9kgx26sI" height="1" width="1"/&gt;</description><a10:updated>2013-03-04T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xueliang Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lingling Chu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Feng-Ling Qing</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00044C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00061C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00061C</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/p8jb61nEnn0/C3NJ00061C</link><title>Improved synthesis of PbSxSe1-x ternary alloy nanocrystals and their nonlinear optical 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=C3NJ00061C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1692-1695&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00061C, Letter&lt;/div&gt;&lt;div&gt;Bao Gao, Min Zhao, Qiang Wang, Kai-Bin Kang, Zhu-Guo Xu, Hao-Li Zhang&lt;br/&gt;We report a facile and low-cost phosphine-free method for synthesizing spherical PbS&lt;small&gt;&lt;sub&gt;&lt;em&gt;x&lt;/em&gt;&lt;/sub&gt;&lt;/small&gt;Se&lt;small&gt;&lt;sub&gt;1-&lt;em&gt;x&lt;/em&gt;&lt;/sub&gt;&lt;/small&gt; NCs with well-controlled size and morphology, and the synthesized NCs show strong optical limiting effects.&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/NJ/~4/p8jb61nEnn0" height="1" width="1"/&gt;</description><a10:updated>2013-02-26T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Bao Gao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Min Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qiang Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kai-Bin Kang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhu-Guo Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hao-Li Zhang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00061C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00033H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00033H</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/QxlwsjVIwJM/C3NJ00033H</link><title>Rhenium(I) polypyridine complexes functionalized with a diaminoaromatic moiety as phosphorescent sensors for nitric oxide</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=C3NJ00033H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1711-1719&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00033H, Paper&lt;/div&gt;&lt;div&gt;Alex Wing-Tat Choi, Che-Shan Poon, Hua-Wei Liu, Heung-Kiu Cheng, Kenneth Kam-Wing Lo&lt;br/&gt;A series of rhenium(&lt;small&gt;I&lt;/small&gt;) polypyridine complexes functionalized with a diaminoaromatic moiety has been developed as phosphorescent sensors for nitric oxide (NO).&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/NJ/~4/QxlwsjVIwJM" height="1" width="1"/&gt;</description><a10:updated>2013-02-26T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Alex Wing-Tat Choi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Che-Shan Poon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hua-Wei Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Heung-Kiu Cheng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kenneth Kam-Wing Lo</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00033H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41127C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41127C</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/Tx0_2_WV-Ck/C3NJ41127C</link><title>From a BODIPY-rhodamine scaffold to a ratiometric fluorescent probe for nitric oxide</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=C3NJ41127C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1688-1691&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ41127C, Letter&lt;/div&gt;&lt;div&gt;Haibo Yu, Liji Jin, Yong Dai, Huaqiang Li, Yi Xiao&lt;br/&gt;Based on a FRET scaffold BRP, a ratiometric probe BRP-NO has been developed for imaging intracellular nitric oxide.&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/NJ/~4/Tx0_2_WV-Ck" height="1" width="1"/&gt;</description><a10:updated>2013-01-16T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Haibo Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Liji Jin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yong Dai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huaqiang Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yi Xiao</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41127C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C2NJ41063J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C2NJ41063J</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/oGgQTHgYm9U/C2NJ41063J</link><title>Fluorescent chemosensors based on 9-cycloheptatrienylidene fluorenes (9-CHFs)</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=C2NJ41063J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1645-1653&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2NJ41063J, Perspective&lt;/div&gt;&lt;div&gt;Binbin Hu, Ping Lu, Yanguang Wang&lt;br/&gt;The chemistry of 9-cycloheptatrienylidene fluorenes and their applications as the fluorescent chemosensors are discussed in this review.&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/NJ/~4/oGgQTHgYm9U" height="1" width="1"/&gt;</description><a10:updated>2013-01-07T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Binbin Hu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ping Lu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yanguang Wang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C2NJ41063J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C2NJ41039G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C2NJ41039G</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/5TPeoaPNAmk/C2NJ41039G</link><title>A facile strategy to enhance the fill factor of ternary blend solar cells by increasing charge carrier mobility</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=C2NJ41039G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1728-1735&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2NJ41039G, Paper&lt;/div&gt;&lt;div&gt;Kun Lu, Jin Fang, Xiangwei Zhu, Han Yan, Denghua Li, Chong'an Di, Yanlian Yang, Zhixiang Wei&lt;br/&gt;Ternary solar cells based on two novel polymers with triethylene glycol and ethylhexyl side chains were investigated, which showed high FF values up to nearly 70%.&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/NJ/~4/5TPeoaPNAmk" height="1" width="1"/&gt;</description><a10:updated>2013-01-04T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Kun Lu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jin Fang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiangwei Zhu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Han Yan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Denghua Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chong'an Di</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yanlian Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhixiang Wei</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C2NJ41039G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C2NJ40842B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C2NJ40842B</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/CMLOcLscoWw/C2NJ40842B</link><title>DIAD-mediated metal-free cross dehydrogenative coupling between tertiary amines and [small alpha]-fluorinated sulfones</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=C2NJ40842B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;37&lt;/b&gt;,1684-1687&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2NJ40842B, Letter&lt;/div&gt;&lt;div&gt;Weizhou Huang, Chuanfa Ni, Yanchuan Zhao, Jinbo Hu&lt;br/&gt;A metal-free oxidative coupling reaction between aliphatic tertiary amines and [small alpha]-fluorinated sulfones leading to [small beta]-fluorinated amines was developed, which represents the first direct fluoroalkylation of C-H bonds with hydrofluorocarbon derivatives (R&lt;small&gt;&lt;sub&gt;F&lt;/sub&gt;&lt;/small&gt;-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/NJ/~4/CMLOcLscoWw" height="1" width="1"/&gt;</description><a10:updated>2012-10-17T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Weizhou Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chuanfa Ni</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yanchuan Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jinbo Hu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C2NJ40842B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00115F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00115F</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/kN6vkoU8yRI/C3NJ00115F</link><title>Dimeric [small mu ]-oxo bridged molybdenum(VI) dioxo complexes as catalysts in the epoxidation of internal and terminal alkenes</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=C3NJ00115F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00115F, Paper&lt;/div&gt;&lt;div&gt;Martina E. Judmaier, Chris H. Sala, Ferdinand Belaj, Manuel Volpe, Nadia C. Mosch-Zanetti&lt;br/&gt;Dimeric complexes are accessible by reaction of [MoO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;(acac)&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;] with tridentate phenol based amine ligands in the presence of water, showing high catalytic activity in the epoxidation of internal and terminal alkenes.&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/NJ/~4/kN6vkoU8yRI" 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/">Martina E. Judmaier</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chris H. Sala</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ferdinand Belaj</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Manuel Volpe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nadia C. Mosch-Zanetti</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00115F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00355H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00355H</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/5FsP214yM54/C3NJ00355H</link><title>Synthesis and Photoluminescence Properties of Polybenzoxazoles Containing Perylenebisimide Functionalized Graphene Nanosheets via Stacking Interactions</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00355H, Paper&lt;/div&gt;&lt;div&gt;Yong Chen, Jun Qian, Xiaoyun Liu, Qixin Zhuang, Zhewen Han&lt;br/&gt;The stable acidic dispersion of reduced graphene oxide (RGO) is prepared by non-covalent functionalization method using perylenebisimide modified fluorinated poly(hydroxyamide) (PTCDA-6FPHA). Then a series of RGO/polybenzoxazoles (PBO) composites were prepared...&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/NJ/~4/5FsP214yM54" 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/">Yong Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jun Qian</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoyun Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qixin Zhuang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhewen Han</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00355H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00012E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00012E</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/dsSoyj3dVn8/C3NJ00012E</link><title>Facile preparation and characterization of luminescent polystyrene composite microspheres</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=C3NJ00012E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00012E, Paper&lt;/div&gt;&lt;div&gt;Zhenxiong Ma, Junliang Liu, Ye Chen, Qitao Zhang, Ming Zhang, Teruhisa Ohno&lt;br/&gt;Luminescent microspheres [poly(St-&lt;em&gt;co&lt;/em&gt;-VBA)-Tb] were easily fabricated from poly(St-&lt;em&gt;co&lt;/em&gt;-VBA) and aqueous Tb(&lt;small&gt;III&lt;/small&gt;) chloride solution in the presence of triethylamine.&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/NJ/~4/dsSoyj3dVn8" 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/">Zhenxiong Ma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Junliang Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ye Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qitao Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ming Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Teruhisa Ohno</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00012E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41177J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41177J</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/6Mbnbkr6HzU/C3NJ41177J</link><title>Hierarchically porous MgAl mixed metal oxide synthesized by sudden decomposition of MgAl layered double hydroxide gel</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=C3NJ41177J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ41177J, Paper&lt;/div&gt;&lt;div&gt;Qi Liu, Jing Yu, Xiaofei Zhang, Jun Wang, Zhanshuang Li, Jideng Zhou, Jingyuan Liu, Zan Gao, Wanlu Yang, Shihui Han&lt;br/&gt;Hierarchically porous MgAl mixed metal oxide was synthesized by the instantaneous combustion of organic by-products from MgAl layered double hydroxide gel.&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/NJ/~4/6Mbnbkr6HzU" 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/">Qi Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jing Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaofei Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jun Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhanshuang Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jideng Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jingyuan Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zan Gao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wanlu Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shihui Han</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41177J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00023K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00023K</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/PeXhNogxoUg/C3NJ00023K</link><title>Structural and magnetic characterization of the tridimensional network [Fe(HCO2)3]n[middle dot]nHCO2H</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=C3NJ00023K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00023K, Paper&lt;/div&gt;&lt;div&gt;Veronica Paredes-Garcia, Ignacio Rojas, Rosa Madrid, Andres Vega, Efren Navarro-Moratalla, Walter Canon-Mancisidor, Evgenia Spodine, Diego Venegas-Yazigi&lt;br/&gt;[Fe(HCO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;)&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt;]&lt;small&gt;&lt;sub&gt;&lt;em&gt;n&lt;/em&gt;&lt;/sub&gt;&lt;/small&gt;[middle dot]&lt;em&gt;n&lt;/em&gt;HCO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;H, a 3D MOF with a 4&lt;small&gt;&lt;sup&gt;12&lt;/sup&gt;&lt;/small&gt;6&lt;small&gt;&lt;sup&gt;3&lt;/sup&gt;&lt;/small&gt; topology, exhibits antiferromagnetic behaviour above 20 K and spin canting below 20 K.&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/NJ/~4/PeXhNogxoUg" height="1" width="1"/&gt;</description><a10:updated>2013-03-15T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Veronica Paredes-Garcia</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ignacio Rojas</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rosa Madrid</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andres Vega</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Efren Navarro-Moratalla</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Walter Canon-Mancisidor</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Evgenia Spodine</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Diego Venegas-Yazigi</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00023K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00148B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00148B</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/xDiloL1mLxU/C3NJ00148B</link><title>Poly-(3-thiopheneacetic acid) coated Fe3O4@LDHs magnetic nanospheres as photocatalyst for efficient photocatalytic disinfection of pathogenic bacteria under solar light irradiation</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00148B, Paper&lt;/div&gt;&lt;div&gt;Kun Shang, Bing Sun, Jianchao Sun, Jun Li, Shiyun Ai&lt;br/&gt;Novel poly-(3-thiopheneacetic acid) coated Fe3O4@LDHs photocatalyst was prepared and used for photocatalytic disinfection of bacterial under solar light irradiation. The influence parameters of photocatalytic antibacterial activity of Fe3O4@PTAA-LDHs photocatalyst were...&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/NJ/~4/xDiloL1mLxU" 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/">Kun Shang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bing Sun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jianchao Sun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jun Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shiyun Ai</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00148B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00192J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00192J</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/GBoBVX_wrlg/C3NJ00192J</link><title>A simply and novel synthesis of 3-(thio)phosphoryl-[small beta]-lactams by radical cyclization</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00192J, Letter&lt;/div&gt;&lt;div&gt;Slawomir Makowiec, Pawel Punda&lt;br/&gt;Radical cyclization of phosphono-acetenamides promoted by manganese (III) acetate leads exclusively to the formation of 3-phosphoryl-[small beta]-lactams. The thiophosphoryl analogues were also prepared using this method. In particular, the presented protocol...&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/NJ/~4/GBoBVX_wrlg" 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/">Slawomir Makowiec</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pawel Punda</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00192J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00003F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00003F</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/AbhLxF3UyDE/C3NJ00003F</link><title>C/N-sensitized self-assembly of mesostructured TiO2 nanospheres with significantly enhanced photocatalytic activity</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00003F, Paper&lt;/div&gt;&lt;div&gt;Xiaoqing Chen&lt;br/&gt;Uniformly carbonaceous and nitrogenous species sensitized TiO2 quantum dots (QDs, ~4 nm) were synthesized through an improved strategy employing oleic acid and oleylamine system, which were further assembled into mesoporous...&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/NJ/~4/AbhLxF3UyDE" 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/">Xiaoqing Chen</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00003F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00406F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00406F</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/xxcyCUoQ4UY/C3NJ00406F</link><title>A Triphenylamine-capped Solution-Processable Wholly Aromatic Organic Molecule with Electrochemical Stability and Its Potential Application in Photovoltaic Devices</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00406F, Paper&lt;/div&gt;&lt;div&gt;Zhiming Wang, Xiaohui Song, Lingling Ma, Ying Feng, Cheng Gu, Xiaojuan Zhang, Ping Lu, Yuguang Ma&lt;br/&gt;A triphenylamine-capped solution-processable wholly aromatic conjugated molecule, TPA-TVBP, was designed and synthesized. It exhibited a high thermodynamic stability and good film forming ability as expected, originating from the absent 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/NJ/~4/xxcyCUoQ4UY" 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/">Zhiming Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaohui Song</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lingling Ma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ying Feng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cheng Gu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaojuan Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ping Lu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuguang Ma</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00406F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00339F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00339F</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/22my6MXkFnQ/C3NJ00339F</link><title>Denitrogen alkene polymerization of bisdiazo compounds by copper(II) catalysts</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=C3NJ00339F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00339F, Letter&lt;/div&gt;&lt;div&gt;Longqiang Xiao, Yan Li, Liqiong Liao, Lijian Liu&lt;br/&gt;Bisdiazo compounds were synthesized and underwent denitrogen alkene polymerization (DNAP) &lt;em&gt;via&lt;/em&gt; the formation of an sp&lt;small&gt;&lt;sup&gt;2&lt;/sup&gt;&lt;/small&gt; carbon bond by copper(&lt;small&gt;II&lt;/small&gt;) catalysts.&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/NJ/~4/22my6MXkFnQ" 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/">Longqiang Xiao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yan Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Liqiong Liao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lijian Liu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00339F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00101F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00101F</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/MXVgchUVaM0/C3NJ00101F</link><title>Preparation of luminescent ZnO nanoparticles modified with aminopropyltriethoxy silane for optoelectronic 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=C3NJ00101F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00101F, Paper&lt;/div&gt;&lt;div&gt;Daniele Costenaro, Fabio Carniato, Giorgio Gatti, Leonardo Marchese, Chiara Bisio&lt;br/&gt;Organo-modified ZnO nanoparticles with tunable luminescent and physico-chemical features have been synthesized through a co-precipitation method and tested as a light-emitting layer in a new generation of LED 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/NJ/~4/MXVgchUVaM0" 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/">Daniele Costenaro</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fabio Carniato</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Giorgio Gatti</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Leonardo Marchese</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chiara Bisio</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00101F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00242J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00242J</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/VwuK7_Ko7PA/C3NJ00242J</link><title>TiN surface modified SnO2 as an efficient anode material for lithium ion batteries</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=C3NJ00242J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00242J, Paper&lt;/div&gt;&lt;div&gt;Mangmang Liu, Xiaowei Li, Hai Ming, Jason Adkins, Xiaomei Zhao, Lele Su, Qun Zhou, Junwei Zheng&lt;br/&gt;TiN modified SnO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; exhibits enhanced electrochemical performance.&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/NJ/~4/VwuK7_Ko7PA" 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/">Mangmang Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaowei Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hai Ming</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jason Adkins</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaomei Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lele Su</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qun Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Junwei Zheng</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00242J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00181D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00181D</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/Fl7ztdGj8-4/C3NJ00181D</link><title>Equilibrium structure and dynamics of organic crystals by Monte Carlo simulation: critical assessment of force fields and comparison with static packing analysis</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=C3NJ00181D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00181D, Paper&lt;/div&gt;&lt;div&gt;Angelo Gavezzotti&lt;br/&gt;Monte Carlo simulation of 63 organic crystal structures by an atom-atom force field reveals details of structural interaction that complement and correct static views of crystal packing. Librational amplitudes and molecular rotation are also portrayed, benzene (figure) being an example.&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/NJ/~4/Fl7ztdGj8-4" 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/">Angelo Gavezzotti</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00181D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00058C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00058C</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/kC7PNKJuzTc/C3NJ00058C</link><title>Reusable [small alpha]-MoO3 nanobelts catalyzes the green and heterogeneous condensation of 1,2-diamines with carbonyl compounds</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=C3NJ00058C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00058C, Paper&lt;/div&gt;&lt;div&gt;Maasoumeh Jafarpour, Abdolreza Rezaeifard, Mahboube Ghahramaninezhad, Tooba Tabibi&lt;br/&gt;Nanobelts of [small alpha]-MoO&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt; have been used as an effective and reusable heterogeneous catalyst for the synthesis of quinoxaline derivatives, pyrido pyrazines and benzimidazole derivatives under mild 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/NJ/~4/kC7PNKJuzTc" height="1" width="1"/&gt;</description><a10:updated>2013-03-27T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Maasoumeh Jafarpour</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Abdolreza Rezaeifard</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mahboube Ghahramaninezhad</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tooba Tabibi</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00058C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00457K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00457K</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/X6goEI7Vp8Y/C3NJ00457K</link><title>On the decarboxylation of 2-methyl-1-tetralone-2-carboxylic acid - oxidation of the enol intermediate by triplet oxygen</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00457K, Letter&lt;/div&gt;&lt;div&gt;Norbert Hoffmann, Abdelkhalek Riahi, Jacques Muzart, Manabu Abe&lt;br/&gt;The formation of 2-methyl-1-tetralone from the metal-free and base-free decarboxylation of 2-methyl-1-tetralone-2-carboxylic acid involves 2-methyl-3,4-dihydro-1-naphthol as intermediate. The reaction of this enol with atmospheric oxygen leads to 2-hydroperoxy-2-methyl-1-tetralone. The oxidation...&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/NJ/~4/X6goEI7Vp8Y" 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/">Norbert Hoffmann</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Abdelkhalek Riahi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jacques Muzart</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Manabu Abe</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00457K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00359K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00359K</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/jar0np3V_qA/C3NJ00359K</link><title>New pyrimidine-based photo-switchable bent-core liquid crystals</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00359K, Paper&lt;/div&gt;&lt;div&gt;Md Lutfor Rahman, Gurumurthy Hyhegde, Mashitah M. Yusoff, Nor Fazli Mohd Abdul Malek, Srinivasa HT, Sandeep Kumar&lt;br/&gt;The first examples of liquid crystalline pyrimidine-based photo-switchable bent-core monomers incorporating the azobenzene as side arms linked with terminal double bonds as polymerizable functional groups are synthesized and characterized. Polarizing...&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/NJ/~4/jar0np3V_qA" 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/">Md Lutfor Rahman</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gurumurthy Hyhegde</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mashitah M. Yusoff</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nor Fazli Mohd Abdul Malek</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Srinivasa HT</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sandeep Kumar</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00359K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00274H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00274H</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/NXxxePPvVTQ/C3NJ00274H</link><title>A novel floating photocatalyst device based on cloth canvas impregnated with iron oxide</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00274H, Paper&lt;/div&gt;&lt;div&gt;Luiz Oliveira, Henrique Oliveira, Adilson Candido da Silva, Joao Paulo de Mesquita, Fabiano Vargas Pereira, Diana Lima, Jose D. Fabris, Flavia Moura&lt;br/&gt;In this paper an innovative and versatile design for a catalytic photoreactor is presented. The photoreactor is based on a floating Polypropylene non-woven fabric canvas (NWF) impregnated with particles 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/NJ/~4/NXxxePPvVTQ" 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/">Luiz Oliveira</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Henrique Oliveira</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Adilson Candido da Silva</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Joao Paulo de Mesquita</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fabiano Vargas Pereira</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Diana Lima</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jose D. Fabris</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Flavia Moura</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00274H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41148F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41148F</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/2vYkJIP3sAA/C3NJ41148F</link><title>Influence of the CH/[small pi] hydrogen bond on the enhancement of circular dichroism (CD) amplitude of 5,7-diene steroids: ergosterol, lumisterol, pirocarciferol, isopirocarciferol and structurally related cyclohexadienes</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=C3NJ41148F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ41148F, Paper&lt;/div&gt;&lt;div&gt;Osamu Takahashi, Yuji Kohno, Motohiro Nishio&lt;br/&gt;Rotational strengths were calculated, by the TD-DFT method, for a series of 5,7-diene steroids, ergosterol, lumisterol, pirocarciferol, isopirocarciferol.&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/NJ/~4/2vYkJIP3sAA" 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/">Osamu Takahashi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuji Kohno</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Motohiro Nishio</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41148F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00199G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00199G</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/AS1Ki-iTtLI/C3NJ00199G</link><title>A new synthetic route towards binuclear 3d-4f complexes, using non-compartmental ligands derived from o-vanillin. Syntheses, crystal structures, magnetic and luminescent 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=C3NJ00199G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00199G, Paper&lt;/div&gt;&lt;div&gt;Masood Sarwar, Augustin M. Madalan, Carmen Tiseanu, Ghenadie Novitchi, Catalin Maxim, Gabriela Marinescu, Dominique Luneau, Marius Andruh&lt;br/&gt;Sixteen new 3d-4f binuclear complexes have been obtained using two Schiff-base ligands &lt;em&gt;o&lt;/em&gt;-vanillin (Hvalampy and Hvalaepy).&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/NJ/~4/AS1Ki-iTtLI" height="1" width="1"/&gt;</description><a10:updated>2013-03-27T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Masood Sarwar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Augustin M. Madalan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Carmen Tiseanu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ghenadie Novitchi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Catalin Maxim</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gabriela Marinescu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dominique Luneau</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Marius Andruh</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00199G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41156G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41156G</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/Sgl8opu0udU/C3NJ41156G</link><title>Preparation of long supramolecular carbon 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=C3NJ41156G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ41156G, Letter&lt;/div&gt;&lt;div&gt;Mohsen Adeli, Ebrahim Mehdipour, Siamak Beyranvand&lt;br/&gt;Supramolecular interactions between the [small pi] system of short carbon nanotubes and periphery aromatic groups of linear-dendritic copolymers lead to long carbon nanotubes.&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/NJ/~4/Sgl8opu0udU" height="1" width="1"/&gt;</description><a10:updated>2013-04-16T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Mohsen Adeli</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ebrahim Mehdipour</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Siamak Beyranvand</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41156G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00171G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00171G</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/l3I8D4iKMwE/C3NJ00171G</link><title>TBAF-catalyzed hydrosilylation for the reduction of aromatic nitriles</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=C3NJ00171G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00171G, Paper&lt;/div&gt;&lt;div&gt;Christoph Bornschein, Svenja Werkmeister, Kathrin Junge, Matthias Beller&lt;br/&gt;The first metal-free hydrosilylation of aromatic nitriles to the corresponding primary amines is presented. Using simple TBAF as a commercially available catalyst and phenylsilane as a hydride source, we performed selective reduction of various aromatic nitriles.&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/NJ/~4/l3I8D4iKMwE" 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/">Christoph Bornschein</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Svenja Werkmeister</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kathrin Junge</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Matthias Beller</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00171G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41126E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41126E</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/oed_3y5Y4qU/C3NJ41126E</link><title>Diferrocenylpyrylium salts and electron rich bispyran from oxidative coupling of ferrocenylpyran. Example of redox systems switched by proton transfer</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=C3NJ41126E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ41126E, Paper&lt;/div&gt;&lt;div&gt;Fatou Ba, Nolwenn Cabon, Pascal Le Poul, Samia Kahlal, Jean-Yves Saillard, Nicolas Le Poul, Stephane Golhen, Bertrand Caro, Francoise Robin-Le Guen&lt;br/&gt;Two ferrocenyl heterocyclic red-ox systems switched by proton transfer were studied by DFT calculations and X-Ray analyses.&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/NJ/~4/oed_3y5Y4qU" height="1" width="1"/&gt;</description><a10:updated>2013-04-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Fatou Ba</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nolwenn Cabon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pascal Le Poul</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Samia Kahlal</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jean-Yves Saillard</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nicolas Le Poul</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stephane Golhen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bertrand Caro</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Francoise Robin-Le Guen</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41126E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41162A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41162A</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/jopgSQNI2tE/C3NJ41162A</link><title>Monodisperse transfer of superparamagnetic nanoparticles from non-polar solvent to aqueous phase</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=C3NJ41162A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ41162A, Paper&lt;/div&gt;&lt;div&gt;Erwin Peng, Eugene Shi Guang Choo, Yang Sheng, Jun Min Xue&lt;br/&gt;Hydrophobic superparamagnetic nanocrystals (MNPs) with good morphology and size distribution control, synthesized through a thermolysis process, were water solubilized with optimized hydrodynamic size by using amphiphilic brush co-polymers PIMA-&lt;em&gt;g&lt;/em&gt;-C&lt;small&gt;&lt;sub&gt;12&lt;/sub&gt;&lt;/small&gt;.&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/NJ/~4/jopgSQNI2tE" 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/">Erwin Peng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Eugene Shi Guang Choo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yang Sheng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jun Min Xue</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41162A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00454F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00454F</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/kbtnO4tTzGU/C3NJ00454F</link><title>Drug specific, tuning of an ionic liquid's hydrophilic-lipophilic balance to improve water solubility of poorly soluble active pharmaceutical ingredients</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00454F, Paper&lt;/div&gt;&lt;div&gt;Parker D. McCrary, Preston A. Beasley, Gabriela Gurau, Asako Narita, Patrick S. Barber, O. Andreea Cojocaru, Robin D. Rogers&lt;br/&gt;Amphotericin B and itraconazole were used to demonstrate that ionic liquids can be designed or chosen to provide tunable hydrophilicity in one ion and lipophilicity in the other allowing one...&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/NJ/~4/kbtnO4tTzGU" 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/">Parker D. McCrary</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Preston A. Beasley</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gabriela Gurau</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Asako Narita</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Patrick S. Barber</creator><creator xmlns="http://purl.org/dc/elements/1.1/">O. Andreea Cojocaru</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Robin D. Rogers</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00454F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00430A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00430A</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/hCt4RW2yi7Y/C3NJ00430A</link><title>Dye-sensitized solar cells based on functionally separated D-[small pi]-A fluorescent dye with aldehyde as electron-accepting group</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00430A, Paper&lt;/div&gt;&lt;div&gt;Yousuke Ooyama, Yuta Hagiwara, Yuichiro Oda, Tomonobu Mizumo, Yutaka Harima, Joji Ohshita&lt;br/&gt;As a new class of D-[small pi]-A dye sensitizer for dye-sensitized solar cells (DSSCs), we have designed and synthesized the functionally separated D-[small pi]-A fluorescent dye YJY-1 with an aldehyde as an...&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/NJ/~4/hCt4RW2yi7Y" 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/">Yousuke Ooyama</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuta Hagiwara</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuichiro Oda</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tomonobu Mizumo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yutaka Harima</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Joji Ohshita</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00430A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00372H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00372H</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/hGoyCgn85Ho/C3NJ00372H</link><title>Water oxidation by nano-layered manganese oxides in the presence of cerium (IV) ammonium nitrate: Important factors and a proposed self-repair mechanism</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00372H, Paper&lt;/div&gt;&lt;div&gt;Mohammad Mahdi Najafpour, Davood Jafarian Sedigh, Babak Pashaei, Sara Nayeri&lt;br/&gt;Nano-sized layered cadmium, magnesium or potassium-Mn oxides were synthesized and characterized by scanning electron microscopy, energy-dispersive X-ray mapping, transmission electron microscopy, X-ray diffraction spectrometry, and atomic absorbtion spectroscopy. These oxides...&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/NJ/~4/hGoyCgn85Ho" 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/">Mohammad Mahdi Najafpour</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Davood Jafarian Sedigh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Babak Pashaei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sara Nayeri</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00372H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00138E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00138E</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/SLHBjaph8fQ/C3NJ00138E</link><title>Catalytic Reduction of p-Nitrophenol over Precious Metals/Supported Highly Ordered Mesoporous Silica</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00138E, Paper&lt;/div&gt;&lt;div&gt;Adel A Ismail, Jafar Al-Sharab, Said El-Sheikha&lt;br/&gt;Precious metals, Au, Pt, and Pd were successfully deposited on highly ordered mesoporous SBA-15. Two different reduction routes were employed to deposit precious metals: 1) under H2, and 2) using...&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/NJ/~4/SLHBjaph8fQ" 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/">Adel A Ismail</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jafar Al-Sharab</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Said El-Sheikha</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00138E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00172E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00172E</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/EVFWmbPUSyI/C3NJ00172E</link><title>High electron transfer capacity of thio-derivatives of tea catechins measured using a water soluble stable free radical and their effects on colon 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=C3NJ00172E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00172E, Paper&lt;/div&gt;&lt;div&gt;Anna Carreras, Juan Antonio Mesa, Marta Cascante, Josep Lluis Torres, Luis Julia&lt;br/&gt;K&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt;TSPTM as a chemical chemosensor of polyphenols in aqueous solutions was selectively sensitive to the pyrogallol moiety of cysteinyl and 2-aminoethylthio derivatives of flavan-3-ols.&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/NJ/~4/EVFWmbPUSyI" height="1" width="1"/&gt;</description><a10:updated>2013-04-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Anna Carreras</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Juan Antonio Mesa</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Marta Cascante</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Josep Lluis Torres</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Luis Julia</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00172E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00233K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00233K</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/EW4JE9JT0G0/C3NJ00233K</link><title>Thioether-tethered bisquinoline derivatives as fluorescent probes for mercury(II) and iron(III) 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=C3NJ00233K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00233K, Letter&lt;/div&gt;&lt;div&gt;Yuji Mikata, Fumie Nakagaki, Kaori Nakanishi&lt;br/&gt;Fluorescence enhancement (OFF-ON), ratiometric and fluorescence quenching (ON-OFF) responses were achieved with the same molecular skeleton, by changing the methoxy substitution pattern.&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/NJ/~4/EW4JE9JT0G0" 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/">Yuji Mikata</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fumie Nakagaki</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kaori Nakanishi</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00233K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ40756J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ40756J</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/EmZO-Obdsso/C3NJ40756J</link><title>Copper(II) ionic liquid catalyzed cyclization-aromatization of hydrazones with dimethyl acetylenedicarboxylate: a green synthesis of fully substituted pyrazoles</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=C3NJ40756J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ40756J, Paper&lt;/div&gt;&lt;div&gt;Shirin Safaei, Iraj Mohammadpoor-Baltork, Ahmad Reza Khosropour, Majid Moghadam, Shahram Tangestaninejad, Valiollah Mirkhani&lt;br/&gt;The Lewis acid room temperature ionic liquid, [&lt;em&gt;n&lt;/em&gt;-Bu&lt;small&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;/small&gt;P][CuBr&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt;], was found to be an efficient and reusable catalyst for three component synthesis of fully substituted pyrazoles.&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/NJ/~4/EmZO-Obdsso" 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/">Shirin Safaei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Iraj Mohammadpoor-Baltork</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ahmad Reza Khosropour</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Majid Moghadam</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shahram Tangestaninejad</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Valiollah Mirkhani</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ40756J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00096F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00096F</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/GWdtbrO_fp0/C3NJ00096F</link><title>Enhanced ethanol sensing of SnO2 hollow micro/nanofibers fabricated by coaxial electrospinning</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=C3NJ00096F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00096F, Paper&lt;/div&gt;&lt;div&gt;Jing Cao, Tong Zhang, Feng Li, Hui Yang, Sen Liu&lt;br/&gt;SnO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; hollow fibers were successfully synthesized by an efficient and facile approach of coaxial electrospinning and presented excellent ethanol sensing properties (an ultra-fast response time that was within 1 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/NJ/~4/GWdtbrO_fp0" height="1" width="1"/&gt;</description><a10:updated>2013-03-28T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jing Cao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tong Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Feng Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hui Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sen Liu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00096F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00182B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00182B</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/NoyROg1fQS8/C3NJ00182B</link><title>Synthesis, molecular structure, electrochemistry and DFT study of a ferrocenyl-substituted 4-quinazolinone and related heterocycles</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=C3NJ00182B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00182B, Paper&lt;/div&gt;&lt;div&gt;Jiri Tauchman, Katerina Hladikova, Filip Uhlik, Ivana Cisarova, Petr Stepnicka&lt;br/&gt;Ferrocenyl-substituted 4(3&lt;em&gt;H&lt;/em&gt;)-quinazolinone and related compounds were prepared and structurally characterised by a combination of spectroscopic methods, X-ray crystallography, cyclic voltammetry and DFT computations.&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/NJ/~4/NoyROg1fQS8" height="1" width="1"/&gt;</description><a10:updated>2013-03-26T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jiri Tauchman</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Katerina Hladikova</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Filip Uhlik</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ivana Cisarova</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Petr Stepnicka</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00182B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41137K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41137K</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/YpEDUKz-HNs/C3NJ41137K</link><title>Synthesis and applications of polymeric N-heterocyclic carbene palladium complex-grafted silica as a novel recyclable nano-catalyst for Heck and Sonogashira coupling 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=C3NJ41137K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ41137K, Paper&lt;/div&gt;&lt;div&gt;Bahman Tamami, Fatemeh Farjadian, Soheila Ghasemi, Hamed Allahyari&lt;br/&gt;A new catalytic system based on polymeric NHC-Pd grafted silica is introduced, which exhibited excellent activity as nano-catalyst in Heck and Sonogashira coupling reactions. The topography of the catalyst was studied by SEM, TEM and AFM.&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/NJ/~4/YpEDUKz-HNs" height="1" width="1"/&gt;</description><a10:updated>2013-03-25T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Bahman Tamami</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fatemeh Farjadian</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Soheila Ghasemi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hamed Allahyari</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41137K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00164D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00164D</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/JNrytnUS0UA/C3NJ00164D</link><title>Metal-organic framework gel with Cd2+ derived from only coordination bonds without intermolecular interactions and its catalytic ability</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00164D, Paper&lt;/div&gt;&lt;div&gt;Jong Hwa Jung, Hyo Hee Lee, Sung Ho Jung, Sunhong Park, Ki-Min Park&lt;br/&gt;A cyclohexane-based ligand (1) as a triconnected linker forms a supramolecular gel in the presence of transition metal ions, particularly Cd2+ and Zn2+. 1 can also be gelated with cadmium...&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/NJ/~4/JNrytnUS0UA" height="1" width="1"/&gt;</description><a10:updated>2013-05-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jong Hwa Jung</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hyo Hee Lee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sung Ho Jung</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sunhong Park</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ki-Min Park</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00164D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00266G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00266G</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/RPQPTpMZhT8/C3NJ00266G</link><title>Cu-In-Zn-S Nanoporous Spheres for Highly Efficient Visible-Light-Driven Photocatalytic Hydrogen Evolution</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00266G, Letter&lt;/div&gt;&lt;div&gt;Xiaosheng Tang, Qiuling Tay, Zhong Chen, Yu Chen, Gregory K. L. Goh, Jun Min Xue&lt;br/&gt;Cu-In-Zn-S (CIZS) nanoporous spheres were prepared by using a facile room temperature method. The band gaps of the CIZS spheres could be tuned by changing the amount of Cu doping....&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/NJ/~4/RPQPTpMZhT8" height="1" width="1"/&gt;</description><a10:updated>2013-05-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaosheng Tang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qiuling Tay</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhong Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yu Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gregory K. L. Goh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jun Min Xue</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00266G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00163F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00163F</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/48FAHnYNfIk/C3NJ00163F</link><title>Synthesis, crystal structures and tautomerism in novel oximes based on hydroxyalkylpyrazolones</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=C3NJ00163F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00163F, Paper&lt;/div&gt;&lt;div&gt;Julio Belmar, Jose Quezada, Claudio A. Jimenez, Pau Diaz-Gallifa, Jorge Pasan, Catalina Ruiz-Perez&lt;br/&gt;Two novel nitroso hydroxyethyl pyrazolones were obtained. The oxime tautomer proved to be more stable in DMSO-&lt;em&gt;d&lt;/em&gt;&lt;small&gt;&lt;sub&gt;6&lt;/sub&gt;&lt;/small&gt; and in CDCl&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt;, equilibrium between &lt;em&gt;E&lt;/em&gt;/&lt;em&gt;Z&lt;/em&gt; diastereomers is observed only in DMSO-&lt;em&gt;d&lt;/em&gt;&lt;small&gt;&lt;sub&gt;6&lt;/sub&gt;&lt;/small&gt;. Single crystal X-ray diffraction data show that tautomeric equilibrium is shifted to the &lt;em&gt;Z&lt;/em&gt;-diastereomer of the oxime, exclusively.&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/NJ/~4/48FAHnYNfIk" height="1" width="1"/&gt;</description><a10:updated>2013-03-26T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Julio Belmar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jose Quezada</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Claudio A. Jimenez</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pau Diaz-Gallifa</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jorge Pasan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Catalina Ruiz-Perez</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00163F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00236E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00236E</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/4WVxvaQf8PU/C3NJ00236E</link><title>A chiral porous cobalt-organic framework based on reinforced sinusoidal-like SBUs involving in situ-generated formate</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00236E, Paper&lt;/div&gt;&lt;div&gt;Qihua Zhao&lt;br/&gt;The assembly of Co(NO3)2[round bullet, filled]6H2O and achiral isonicotinic acid (HIN) under solvo(hydro)thermal conditions yields a three-dimensional chiral Co-based MOF, {[Co6([small mu ]3OH)2(IN)4(HCOO)6][round bullet, filled]4DMF[round bullet, filled]5H2O}n (1). Polymer 1 consists of a reinforced sinusoidal-like hydroxyl/formate/carboxylate mixed-bridged chain...&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/NJ/~4/4WVxvaQf8PU" 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/">Qihua Zhao</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00236E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00241A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00241A</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/OnWfr2Yi6Mw/C3NJ00241A</link><title>Synthesis, Photochromic Properties and Thermal Bleaching Kinetics of Pyrazolone Phenylsemicarbazones Containing a Thiophene Ring</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00241A, Paper&lt;/div&gt;&lt;div&gt;Hubin Sun, Lang Liu, Donglin Wu, dianzeng Jia, jixi guo&lt;br/&gt;Five novel pyrazolone derivatives containing a thiophene ring, 1-phenyl-3-(2-thiophenyl)-4-(3-bromobenzal)-5-hydroxypyrazole phenyl- semicarbazone (P2-Th3BrBP-PSC, 1) /1-phenyl-3-(2-thiophenyl)-4-(3-chlorobenzal)-5-hydroxypyrazole phenylsemicarbazone (P2-Th3Cl BP-PSC, 2) /1-phenyl-3-(2-thiophenyl)-4-benzal-5-hydroxypyrazole phenylsemicarbazone (P2-ThBP-PSC, 3) /1-phenyl-3-(2-thiophenyl)-4-(4-bromobenzal)-5-hydroxypyrazole phenylsemicarbazone (P2-Th4BrBP-PSC, 4) /1-phenyl-3-(2-thiophenyl)-4-(4-chlorobenzal)-5-hydro- xypyrazole phenylsemicarbazone (P2-Th4ClBP-PSC,...&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/NJ/~4/OnWfr2Yi6Mw" 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/">Hubin Sun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lang Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Donglin Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">dianzeng Jia</creator><creator xmlns="http://purl.org/dc/elements/1.1/">jixi guo</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00241A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00288H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00288H</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/fUyAaZf8WYI/C3NJ00288H</link><title>DNA Three-Way Junction - Ruthenium Complex Assemblies</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00288H, Paper&lt;/div&gt;&lt;div&gt;Joris Irvoas, Arielle Noirot, Nadia Chouini-Lalanne, Olivier Reynes, Valerie Sartor&lt;br/&gt;Three-way junction building blocks were designed to construct novel 2D Ruthenium-DNA assemblies. Discrete three-branched DNA motifs were formed with 1 to 3 sticky ends of 14-, 20- and/or 24-mer nucleotides....&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/NJ/~4/fUyAaZf8WYI" 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/">Joris Irvoas</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Arielle Noirot</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nadia Chouini-Lalanne</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Olivier Reynes</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Valerie Sartor</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00288H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00399J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00399J</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/iwXHDpXQNDI/C3NJ00399J</link><title>Cucurbiturils as Promising Hydrogen Storage Materials: A Case Study of Cucurbit[7]uril</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00399J, Paper&lt;/div&gt;&lt;div&gt;Pratim Chattaraj, Sudip Pan, Mondal Sukanta&lt;br/&gt;We have assessed the hydrogen storage capability of cucurbiturils, which are experimentally available. For this purpose, first we have investigated the hydrogen binding ability of the repeating unit and prompted...&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/NJ/~4/iwXHDpXQNDI" 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/">Pratim Chattaraj</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sudip Pan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mondal Sukanta</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00399J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00186E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00186E</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/a8lXC9kYqKU/C3NJ00186E</link><title>The Reaction of NH-Indazoles with 1-Fluoro-2,4-dinitrobenzene: The Unusual Formation of Benzotriazole-N-oxides</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00186E, Paper&lt;/div&gt;&lt;div&gt;Ibon Alkorta, Fernando Cossio, Jose Elguero, Nieves Fresno, Laura Hernandez-Folgado, Santiago Garcia-Granda, Laura Menendez-Taboada, Ruth Perez-Fernandez, Felipe Reviriego, Lucia Vazquez-Vinuela&lt;br/&gt;When N-unsubstituted indazoles, like indazole itself, reacted with 1-fluoro-2,4-dinitrobenzene or 1-chloro-2,4,6-trinitrobenzene, three products were obtained whose structures were determined by X-ray diffraction. Besides the two N-substituted nitroaryl derivatives, a third...&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/NJ/~4/a8lXC9kYqKU" 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/">Ibon Alkorta</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fernando Cossio</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jose Elguero</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nieves Fresno</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Laura Hernandez-Folgado</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Santiago Garcia-Granda</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Laura Menendez-Taboada</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ruth Perez-Fernandez</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Felipe Reviriego</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lucia Vazquez-Vinuela</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00186E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00072A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00072A</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/YOeCKv2CweU/C3NJ00072A</link><title>Design and synthesis of sugar-triazole low molecular weight gels as mercury ion sensor</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00072A, Paper&lt;/div&gt;&lt;div&gt;Arasappan Hemamalini, Thangamuthu Mohan Das&lt;br/&gt;A series of gel forming symmetrical bis-sugar-triazoles has been developed for the recognition of Hg2+ ion. Preferential interaction of Hg2+ ion with organogelator based chemosensor 3f lead to the changes...&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/NJ/~4/YOeCKv2CweU" 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/">Arasappan Hemamalini</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Thangamuthu Mohan Das</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00072A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00111C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00111C</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/jdBxceD-zpw/C3NJ00111C</link><title>Salen complexes based on 1,4-diaminocyclohexane and their exploitation for the polymerisation of rac-lactide</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=C3NJ00111C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00111C, Paper&lt;/div&gt;&lt;div&gt;Stuart L. Hancock, Mary F. Mahon, Matthew D. Jones&lt;br/&gt;A series of Al(&lt;small&gt;III&lt;/small&gt;) and Ti(&lt;small&gt;IV&lt;/small&gt;) complexes based on a &lt;em&gt;trans&lt;/em&gt;-1,4-diaminocyclohexane backbone have been prepared for the production of 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/NJ/~4/jdBxceD-zpw" 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/">Stuart L. Hancock</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mary F. Mahon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Matthew D. Jones</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00111C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00174A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00174A</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/7zvhmVjfbys/C3NJ00174A</link><title>Improved microwave-assisted ligand-free Suzuki-Miyaura cross-coupling of 5-iodo-2[prime or minute]-deoxyuridine in pure 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=C3NJ00174A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00174A, Paper&lt;/div&gt;&lt;div&gt;Shawn Gallagher-Duval, Gwenaelle Herve, Guillaume Sartori, Gerald Enderlin, Christophe Len&lt;br/&gt;Unprecedented microwave-assisted ligand-free Suzuki-Miyaura cross-coupling of 5-iodo-2[prime or minute]-deoxyuridine in pure water has been developed providing the corresponding 5-arylated uridine analogues in moderate to high yields within short reaction times.&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/NJ/~4/7zvhmVjfbys" 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/">Shawn Gallagher-Duval</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gwenaelle Herve</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guillaume Sartori</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gerald Enderlin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christophe Len</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00174A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00078H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00078H</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/TTZxrYeA9U8/C3NJ00078H</link><title>Synthesis, photophysics and electrochemistry of novel, nitrogen-containing heterocyclic derivatives</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=C3NJ00078H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ00078H, Paper&lt;/div&gt;&lt;div&gt;Danuta Branowska, Bartosz Chaciak, Olga Siuchta, Ewa Olender, Przemyslaw Ledwon, Mieczyslaw Lapkowski, Eugenij Poronik, Waldemar Wysocki, Zbigniew Karczmarzyk, Lukasz Skora, Michal Filapek, Stanislaw Krompiec, Zofia Urbanczyk-Lipkowska, Przemyslaw Kalicki&lt;br/&gt;A series of oligothiophenes bearing a 1,2,4-triazine ring were synthesized and their highly conjugated properties were confirmed.&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/NJ/~4/TTZxrYeA9U8" 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/">Danuta Branowska</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bartosz Chaciak</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Olga Siuchta</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ewa Olender</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Przemyslaw Ledwon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mieczyslaw Lapkowski</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Eugenij Poronik</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Waldemar Wysocki</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zbigniew Karczmarzyk</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lukasz Skora</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michal Filapek</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stanislaw Krompiec</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zofia Urbanczyk-Lipkowska</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Przemyslaw Kalicki</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ00078H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41169A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41169A</guid><link>http://feeds.rsc.org/~r/rss/NJ/~3/EOwiyyZezDA/C3NJ41169A</link><title>The effect of carboxylic acids on glycine polymorphism, salt and co-crystal formation. A comparison of different crystallisation techniques</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=C3NJ41169A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;New J. Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NJ41169A, Paper&lt;/div&gt;&lt;div&gt;Evgeniy A. Losev, Mikhail A. Mikhailenko, Andrey F. Achkasov, Elena V. Boldyreva&lt;br/&gt;Different phases were found to crystallise from a mixture of the same starting components (glycine and a carboxylic acid), depending on the preparative technique: slow evaporation of solutions at ambient conditions, spray drying, "fast" and "slow" anti-solvent crystallisation and dry co-grinding.&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/NJ/~4/EOwiyyZezDA" height="1" width="1"/&gt;</description><a10:updated>2013-03-26T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Evgeniy A. Losev</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mikhail A. Mikhailenko</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrey F. Achkasov</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Elena V. Boldyreva</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NJ/C3NJ41169A</feedburner:origLink></item></channel></rss>
