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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 - Chem. Sci. latest articles</title><link>http://pubs.rsc.org/en/Journals/Journal/SC</link><description>RSC - Chem. Sci. latest articles</description><copyright>Copyright (c)  The Royal Society of Chemistry</copyright><lastBuildDate>Tue, 14 Feb 2012 10:03:17 Z</lastBuildDate><category>RSC - Chem. Sci. latest articles</category><image><url>http://pubs.rsc.org/content/NewImages/rsc_publishing_logo.gif</url><title>RSC - Chem. Sci. latest articles</title><link>http://pubs.rsc.org/en/Journals/Journal/SC</link></image><atom10:link xmlns:atom10="http://www.w3.org/2005/Atom" rel="self" type="application/rss+xml" href="http://feeds.rsc.org/rss/SC" /><feedburner:info uri="rss/sc" /><atom10:link xmlns:atom10="http://www.w3.org/2005/Atom" rel="hub" href="http://pubsubhubbub.appspot.com/" /><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01031C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01031C</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/G6wyrOAuzjU/C2SC01031C</link><title>Osmium(VI) nitrido complexes bearing azole heterocycles: a new class of antitumor agents</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=C2SC01031C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01031C, Edge Article&lt;/div&gt;&lt;div&gt;Wen-Xiu Ni, Wai-Lun Man, Shek-Man Yiu, Man Ho, Myra Ting-Wai Cheung, Chi-Chiu Ko, Chi-Ming Che, Yun-Wah Lam, Tai-Chu Lau&lt;br/&gt;A series of eight nitridoosmium(&lt;small&gt;VI&lt;/small&gt;) complexes bearing chloro and Hazole ligands has been prepared and characterized. The osmium(&lt;small&gt;VI&lt;/small&gt;) nitrido complexes 1-4 bearing pyrazole ligands show promising anti-cancer properties.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/SC/~4/G6wyrOAuzjU" height="1" width="1"/&gt;</description><a10:updated>2012-02-03T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Wen-Xiu Ni</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wai-Lun Man</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shek-Man Yiu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Man Ho</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Myra Ting-Wai Cheung</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chi-Chiu Ko</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chi-Ming Che</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yun-Wah Lam</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tai-Chu Lau</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01031C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00764A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00764A</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/VAZpXcHLu3w/C2SC00764A</link><title>Hydrogen bonds with fluorine. Studies in solution, in gas phase and by computations, conflicting conclusions from crystallographic analyses</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=C2SC00764A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00764A, Perspective&lt;/div&gt;&lt;div&gt;Hans-Jorg Schneider&lt;br/&gt;Hydrogen bonds with organic fluorine and other halogens as acceptors show a consistent picture in gas and solution phase in agreement with computations, whereas conflicting conclusions were drawn from crystallographic 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/SC/~4/VAZpXcHLu3w" height="1" width="1"/&gt;</description><a10:updated>2012-01-12T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hans-Jorg Schneider</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00764A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01083F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01083F</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/7sYFnmgEV0o/C2SC01083F</link><title>Ni(0) or Cu(0) catalyzed cleavage of unactivated C-Cl bond of 2-chloro-1,1,1-trifluoroethane (HCFC-133a) via Single Electron Transfer (SET) process</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01083F, Edge Article&lt;/div&gt;&lt;div&gt;Qing-Yun Chen&lt;br/&gt;The reductive cleavage of unactivated carbon-chlorine bond of 2-chloro-1,1,1-trifluoroethane (HCFC-133a) via single electron transfer (SET) process using transition-metal-catalyzation has been achieved. Ni(0) or Cu(0) catalytic system afford 1,1,1-trifluoroethane(HFC-143a) or 1,1-difluoroethylene(VDF)...&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/SC/~4/7sYFnmgEV0o" height="1" width="1"/&gt;</description><a10:updated>2012-02-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Qing-Yun Chen</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01083F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01133F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01133F</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/rKHuoZicpuQ/C2SC01133F</link><title>Substituent effects in a series of 1,7-C60(RF)2 compounds (RF = CF3, C2F5, n-C3F7, i-C3F7, n-C4F9, s-C4F9, n-C8F17): Electron affinities, reduction potentials, and E(LUMO) values are not always correlated</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01133F, Edge Article&lt;/div&gt;&lt;div&gt;Igor V Kuvychko, James B. Whitaker, Bryon W. Larson, Travis C. Folsom, Natalia B. Shustova, Stanislav M. Avdoshenko, Yu-Sheng Chen, Hui Wen, Xuebin Wang, Lothar Dunsch, Alexey A Popov, Olga V. Boltalina, Steven H Strauss&lt;br/&gt;A series of seven structurally-similar compounds with different pairs of RF groups were prepared, characterized spectroscopically, and studied by electrochemical methods (cyclic and square-wave voltammetry), low-temperature anion photoelectron spectroscopy, and...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/SC/~4/rKHuoZicpuQ" height="1" width="1"/&gt;</description><a10:updated>2012-02-10T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Igor V Kuvychko</creator><creator xmlns="http://purl.org/dc/elements/1.1/">James B. Whitaker</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bryon W. Larson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Travis C. Folsom</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Natalia B. Shustova</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stanislav M. Avdoshenko</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yu-Sheng Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hui Wen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xuebin Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lothar Dunsch</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alexey A Popov</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Olga V. Boltalina</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Steven H Strauss</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01133F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01134D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01134D</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/FGIiH8uzg5A/C2SC01134D</link><title>Rh2(S-PTTL)3TPA-A Mixed Ligand Dirhodium(II) Catalyst for Enantioselective Reactions of [small alpha]-Alkyl-[small alpha]-Diazoesters</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01134D, Edge Article&lt;/div&gt;&lt;div&gt;Joseph Fox, David Boruta, Olga Dmitrenko, Glenn Yap&lt;br/&gt;Herein we report the synthesis of the mixed ligand paddlewheel complex dirhodium(II) tris[N-phthaloyl-(S)-tert-leucinate] triphenylacetate, Rh2(S-PTTL)3TPA, the structure of which bears similarity to the chiral crown complex Rh2(S-PTTL)4. Rh2(S-PTTL)3TPA engages substrate...&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/SC/~4/FGIiH8uzg5A" height="1" width="1"/&gt;</description><a10:updated>2012-02-10T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Joseph Fox</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David Boruta</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Olga Dmitrenko</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Glenn Yap</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01134D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00931E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00931E</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/-GPS6lDmJZg/C2SC00931E</link><title>Synthesis of a diniobium tetraphosphorus complex by a 2(3-1) process</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=C2SC00931E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00931E, Edge Article&lt;/div&gt;&lt;div&gt;Alexandra Velian, Christopher C. Cummins&lt;br/&gt;The mononuclear diphosphorus complex P&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;Nb(ODipp)&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt;, proposed to form transiently upon formal P&lt;small&gt;&lt;sup&gt;-&lt;/sup&gt;&lt;/small&gt; abstraction from [P&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt;Nb(ODipp)&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt;]&lt;small&gt;&lt;sup&gt;-&lt;/sup&gt;&lt;/small&gt;, undergoes irreversible dimerization to [P&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt;Nb(ODipp)&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt;]&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; and is alternatively trapped by a 1,3-cyclohexadiene &lt;i&gt;in situ&lt;/i&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/SC/~4/-GPS6lDmJZg" height="1" width="1"/&gt;</description><a10:updated>2012-01-20T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Alexandra Velian</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christopher C. Cummins</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00931E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC20041D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC20041D</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/gC09UErlOJs/C2SC20041D</link><title>Tunable transmembrane chloride transport by bis-indolylureas</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC20041D, Edge Article&lt;/div&gt;&lt;div&gt;Philip A Gale, Vitor Felix&lt;br/&gt;A series of bis-indolylureas have been found to mediate chloride transport across vesicle bilayers. The anion transport activity of these receptors may be readily modulated by small structural changes to...&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/SC/~4/gC09UErlOJs" height="1" width="1"/&gt;</description><a10:updated>2012-02-09T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Philip A Gale</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Vitor Felix</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC20041D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC20096A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC20096A</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/zbbTkIlNuKk/C2SC20096A</link><title>Asymmetric Diels-Alder Reaction of beta,beta-Disubstituted Enals with Chromone-Fused Dienes and Cascade: Construction of Collections with High Molecular Complexity and Skeletal Diversit</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC20096A, Edge Article&lt;/div&gt;&lt;div&gt;Ying-Chun Chen, Jun-Long Li, Si-Li Zhou, Peng-Qiao Chen, Lin Dong, Tian-Yu Liu&lt;br/&gt;The first asymmetric inverse-electron-demand Diels-Alder reaction of chromone-fused dienes and beta,beta-disubstituted alfa,beta-unsaturated aldehydes has been developed via dienamine catalysis. Different domino or sequential transformations could be carried out for electron-deficient...&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/SC/~4/zbbTkIlNuKk" height="1" width="1"/&gt;</description><a10:updated>2012-02-09T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ying-Chun Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jun-Long Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Si-Li Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Peng-Qiao Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lin Dong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tian-Yu Liu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC20096A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01103D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01103D</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/XiUu7PASwcc/C2SC01103D</link><title>Order-of-Magnitude Enhancement of an Enzymatic Hydrogen-Air Fuel Cell based on Pyrenyl Carbon Nanostructures</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01103D, Edge Article&lt;/div&gt;&lt;div&gt;Fraser A Armstrong, Sadagopan Krishnan&lt;br/&gt;A fuel cell featuring two enzymes as electrocatalysts on specially modified electrodes - an O2-tolerant hydrogenase for the anode and bilirubin oxidase for the cathode - produces more than 0.1...&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/SC/~4/XiUu7PASwcc" height="1" width="1"/&gt;</description><a10:updated>2012-02-09T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Fraser A Armstrong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sadagopan Krishnan</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01103D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00023G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00023G</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/uUW2YqI79Qc/C2SC00023G</link><title>Engineering Conjugation in Para-Phenylene-Bridged Porphyrin Tapes</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00023G, Edge Article&lt;/div&gt;&lt;div&gt;Milosz Pawlicki, Mitsuhiko Morisue, Nicola Davis, Daniel McLean, Joy E. Haley, Erich Beuerman, Mikhail Drobijev, Aleksander Rebane, Amber L Thompson, Sofia I Pascu, Gianluca Accorsi, Nicola Armaroli, Harry L Anderson&lt;br/&gt;We report the synthesis of 7 new para-phenylene-bridged zinc porphyrin dimers, five of which have been characterized by single-crystal X-ray analysis. A variety of links were tested for holding the...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/SC/~4/uUW2YqI79Qc" height="1" width="1"/&gt;</description><a10:updated>2012-02-09T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Milosz Pawlicki</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mitsuhiko Morisue</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nicola Davis</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Daniel McLean</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Joy E. Haley</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Erich Beuerman</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mikhail Drobijev</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Aleksander Rebane</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Amber L Thompson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sofia I Pascu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gianluca Accorsi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nicola Armaroli</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Harry L Anderson</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00023G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01016J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01016J</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/862sSyXwL40/C2SC01016J</link><title>Visible-light-mediated photochemistry: accelerating Ru(bpy)32+-catalyzed reactions in continuous flow</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=C2SC01016J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01016J, Edge Article&lt;/div&gt;&lt;div&gt;Farhan R. Bou-Hamdan, Peter H. Seeberger&lt;br/&gt;The first application of visible-light-mediated synthetic photochemistry in continuous flow is described. Using an operationally simple photoreactor design, several Ru(bpy)&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt;&lt;small&gt;&lt;sup&gt;2+&lt;/sup&gt;&lt;/small&gt;-catalyzed transformations were performed with 10-50 fold rate enhancement over the corresponding batch methods.&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/SC/~4/862sSyXwL40" height="1" width="1"/&gt;</description><a10:updated>2012-02-09T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Farhan R. Bou-Hamdan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Peter H. Seeberger</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01016J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01100J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01100J</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/IhkCXQWnOkE/C2SC01100J</link><title>Inhibitory action of macrocyclic platiniferous chelators on metal-induced A[small beta] aggregation</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2SC01100J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01100J, Edge Article&lt;/div&gt;&lt;div&gt;Xiaohui Wang, Xiaoyong Wang, Changli Zhang, Yang Jiao, Zijian Guo&lt;br/&gt;Macrocyclic platiniferous chelators show significant inhibition against the metal-induced A&lt;i&gt;[small beta]&lt;/i&gt; aggregation; an intramolecular synergy may account for the function.&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/SC/~4/IhkCXQWnOkE" height="1" width="1"/&gt;</description><a10:updated>2012-01-26T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaohui Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoyong Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Changli Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yang Jiao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zijian Guo</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01100J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00771A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00771A</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/oEhsXUeJvl8/C2SC00771A</link><title>Molecular engineering of chromophores for combined second-harmonic and two-photon fluorescence in cellular imaging</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=C2SC00771A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00771A, Edge Article&lt;/div&gt;&lt;div&gt;Evelien De Meulenaere, Wei-Qiang Chen, Stijn Van Cleuvenbergen, Mei-Ling Zheng, Sotiris Psilodimitrakopoulos, Rik Paesen, Jean-Marc Taymans, Marcel Ameloot, Jos Vanderleyden, Pablo Loza-Alvarez, Xuan-Ming Duan, Koen Clays&lt;br/&gt;We have designed, synthesized and characterized new carbazole-based dyes for combined two-photon fluorescence and second-harmonic generation microscopy, one of which performs very well and selectively in mitochondria in both channels.&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/SC/~4/oEhsXUeJvl8" height="1" width="1"/&gt;</description><a10:updated>2012-01-25T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Evelien De Meulenaere</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wei-Qiang Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stijn Van Cleuvenbergen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mei-Ling Zheng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sotiris Psilodimitrakopoulos</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rik Paesen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jean-Marc Taymans</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Marcel Ameloot</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jos Vanderleyden</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pablo Loza-Alvarez</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xuan-Ming Duan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Koen Clays</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00771A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01017H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01017H</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/5xwdblR1kjc/C2SC01017H</link><title>Imidazolidines as hydride sources for the formation of late transition-metal monohydrides</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=C2SC01017H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01017H, Edge Article&lt;/div&gt;&lt;div&gt;Macarena Poyatos, Amparo Prades, Sergio Gonell, Dmitri G. Gusev, Eduardo Peris&lt;br/&gt;Cyclic aminals act as efficient reducing agents for the conversion of metal halides to the corresponding hydrides.&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/SC/~4/5xwdblR1kjc" height="1" width="1"/&gt;</description><a10:updated>2012-01-19T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Macarena Poyatos</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Amparo Prades</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sergio Gonell</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dmitri G. Gusev</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Eduardo Peris</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01017H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01033J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01033J</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/SyToMSdXhtc/C2SC01033J</link><title>Thermally stable N2 and H2 adducts of cationic nickel(II)</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=C2SC01033J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01033J, Edge Article&lt;/div&gt;&lt;div&gt;Charlene Tsay, Jonas C. Peters&lt;br/&gt;The first examples of thermally stable molecular dihydrogen adducts of nickel were synthesized from rare dinitrogen adduct precursors.&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/SC/~4/SyToMSdXhtc" height="1" width="1"/&gt;</description><a10:updated>2012-01-19T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Charlene Tsay</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jonas C. Peters</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01033J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01081J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01081J</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/8FUT0UZdz8s/C2SC01081J</link><title>Mechanistic understanding of Rh-catalyzed N-sulfonylaldimine insertion into aryl C-H bonds</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=C2SC01081J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01081J, Edge Article&lt;/div&gt;&lt;div&gt;Yang Li, Xi-Sha Zhang, Hu Li, Wen-Hua Wang, Kang Chen, Bi-Jie Li, Zhang-Jie Shi&lt;br/&gt;A detailed investigation is presented to understand the catalytic pathway of our recently reported Rh(&lt;small&gt;III&lt;/small&gt;)-catalyzed &lt;i&gt;N&lt;/i&gt;-tosylaldimine insertion into aryl C-H bonds.&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/SC/~4/8FUT0UZdz8s" height="1" width="1"/&gt;</description><a10:updated>2012-01-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yang Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xi-Sha Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hu Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wen-Hua Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kang Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bi-Jie Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhang-Jie Shi</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01081J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01088G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01088G</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/LBLNZngeaqc/C2SC01088G</link><title>Insight into peptide self-assembly from anisotropic rotational diffusion derived from 13C NMR relaxation</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=C2SC01088G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01088G, Edge Article&lt;/div&gt;&lt;div&gt;Davy Sinnaeve, Marc-Andre Delsuc, Jose C. Martins, Bruno Kieffer&lt;br/&gt;The dependency of &lt;small&gt;&lt;sup&gt;13&lt;/sup&gt;&lt;/small&gt;C NMR relaxation rates on molecular anisotropy provides insight into the supramolecular structure of a self-assembling peptide.&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/SC/~4/LBLNZngeaqc" height="1" width="1"/&gt;</description><a10:updated>2012-01-26T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Davy Sinnaeve</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Marc-Andre Delsuc</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jose C. Martins</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bruno Kieffer</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01088G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01004F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01004F</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/twySXYYrCFk/C2SC01004F</link><title>Novel self-assembled dynamic [2]catenanes interlocked by the quadruple hydrogen bonding ureidopyrimidinone motif</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=C2SC01004F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01004F, Edge Article&lt;/div&gt;&lt;div&gt;Tangxin Xiao, Shao-Lu Li, Yajie Zhang, Chen Lin, Bingjie Hu, Xinchao Guan, Yihua Yu, Juli Jiang, Leyong Wang&lt;br/&gt;Novel dynamic donor-acceptor [2]catenanes interlocked by the quadruple hydrogen bonding ureidopyrimidinone motif have been constructed.&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/SC/~4/twySXYYrCFk" height="1" width="1"/&gt;</description><a10:updated>2012-01-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Tangxin Xiao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shao-Lu Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yajie Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chen Lin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bingjie Hu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xinchao Guan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yihua Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Juli Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Leyong Wang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01004F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01093C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01093C</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/44NKJr9HYZE/C2SC01093C</link><title>Rhodium/diene-catalyzed tandem 1,4-shift/1,4-addition of (E)-1,2-diphenylethenylboronic acid to enones: density functional theory modeling and asymmetric catalysis</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=C2SC01093C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01093C, Edge Article&lt;/div&gt;&lt;div&gt;Keigo Sasaki, Takahiro Nishimura, Ryo Shintani, Eric Assen B. Kantchev, Tamio Hayashi&lt;br/&gt;A 1,4-rhodium shift was observed during the addition of (&lt;i&gt;E&lt;/i&gt;)-1,2-diphenylethenylboronic acid to 2-cyclohexenone leading to a product incorporating a 2-((&lt;i&gt;E&lt;/i&gt;)-2-phenylethenyl)phenyl group.&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/SC/~4/44NKJr9HYZE" height="1" width="1"/&gt;</description><a10:updated>2012-01-17T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Keigo Sasaki</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Takahiro Nishimura</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ryo Shintani</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Eric Assen B. Kantchev</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tamio Hayashi</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01093C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01068B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01068B</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/KE2yirBW5UY/C2SC01068B</link><title>Rh(I)-catalyzed enantioselective intramolecular hydroarylation of unactivated ketones with aryl pinacolboronic esters</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=C2SC01068B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01068B, Edge Article&lt;/div&gt;&lt;div&gt;Gary M. Gallego, Richmond Sarpong&lt;br/&gt;Aryl pinacolboronic esters effectively add in an intramolecular 1,2 fashion into unactivated ketone groups in the presence of the rhodium complexes [Rh(cod)(MeCN)&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;]BF&lt;small&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;/small&gt; and a tertiary amine base or [Rh(cod)(OH)]&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; and bisphosphine ligands, which induce enantioselectivity.&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/SC/~4/KE2yirBW5UY" height="1" width="1"/&gt;</description><a10:updated>2012-01-17T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Gary M. Gallego</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Richmond Sarpong</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01068B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01030E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01030E</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/nH4HB2cj558/C2SC01030E</link><title>Quantum chemical characterization of the mechanism of an iron-based water oxidation catalyst</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2SC01030E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01030E, Edge Article&lt;/div&gt;&lt;div&gt;Mehmed Z. Ertem, Laura Gagliardi, Christopher J. Cramer&lt;br/&gt;Theoretical models are used to demonstrate a catalytic cycle for the generation of O&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; from an iron(&lt;small&gt;III&lt;/small&gt;)-centered tetraamido macrocycle in water that is consistent with experimentally observed energetics in the presence of a sacrificial oxidant. Modification of the TAML ligand to reduce the likely instability of the non-innocent aromatic radical may prove useful in future catalyst design.&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/SC/~4/nH4HB2cj558" height="1" width="1"/&gt;</description><a10:updated>2012-01-12T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Mehmed Z. Ertem</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Laura Gagliardi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christopher J. Cramer</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01030E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00436D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00436D</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/QHXYNYr1PJ0/C2SC00436D</link><title>Fabrication and enhanced photocatalytic activity of inorganic core-shell nanofibers produced 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=C2SC00436D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00436D, Edge Article&lt;/div&gt;&lt;div&gt;Xiaohui Peng, Alexander C. Santulli, Eli Sutter, Stanislaus S. Wong&lt;br/&gt;We show that highly uniform SnO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;/TiO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; coaxial nanoscale fibers with a tunable internal morphology can be prepared in one step by means of coaxial electrospinning.&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/SC/~4/QHXYNYr1PJ0" height="1" width="1"/&gt;</description><a10:updated>2012-02-07T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaohui Peng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alexander C. Santulli</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Eli Sutter</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stanislaus S. Wong</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00436D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00754A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00754A</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/dqgqIBacCm4/C2SC00754A</link><title>Oxygen Activation in Extradiol Catecholate Dioxygenases - A Density Functional Study</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00754A, Edge Article&lt;/div&gt;&lt;div&gt;Shengfa Ye, Gemma J Christian, Frank Neese&lt;br/&gt;Recent trapping and spectroscopic characterization of an O2 adduct for the non-heme enzyme Homoprotocatechuate 2,3-dioxygenase (HPCD) demonstrates it to be a FeIII-superoxo species. This proposal is in direct opposition to...&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/SC/~4/dqgqIBacCm4" height="1" width="1"/&gt;</description><a10:updated>2012-02-07T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Shengfa Ye</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gemma J Christian</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Frank Neese</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00754A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01034H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01034H</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/z6o5UNnHUQM/C2SC01034H</link><title>Towards organic film passivation of germanium wafers using diazonium salts: mechanism and ambient stability</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01034H, Edge Article&lt;/div&gt;&lt;div&gt;Xavier Lefevre, Olivier Segut, Pascale Jegou, Serge Palacin, Bruno Jousselme&lt;br/&gt;Germanium is well-known for its good electronic properties but also the poor passivation quality of its natural or thermally-grown oxide layer. The robust passivation of Ge surfaces is thus a...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/SC/~4/z6o5UNnHUQM" height="1" width="1"/&gt;</description><a10:updated>2012-02-07T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xavier Lefevre</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Olivier Segut</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pascale Jegou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Serge Palacin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bruno Jousselme</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01034H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01082H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01082H</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/QKo_g-n3mAQ/C2SC01082H</link><title>Kinetic correlation between aldehyde/enamine stereoisomers in reactions between aldehydes with [small alpha]-stereocenters and chiral pyrrolidine-based 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=C2SC01082H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01082H, Edge Article&lt;/div&gt;&lt;div&gt;Jordi Bures, Alan Armstrong, Donna G. Blackmond&lt;br/&gt;Reaction between aldehydes with [small alpha]-stereocenters and pyrrolidine-based catalysts leads to "kinetically stereospecific" formation of &lt;i&gt;E&lt;/i&gt; and &lt;i&gt;Z&lt;/i&gt; enamines.&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/SC/~4/QKo_g-n3mAQ" height="1" width="1"/&gt;</description><a10:updated>2012-01-26T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jordi Bures</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alan Armstrong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Donna G. Blackmond</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01082H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00834C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00834C</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/cayCvZsMA1I/C2SC00834C</link><title>Novel global-like second-order nonlinear optical dendrimers: convenient synthesis through powerful click chemistry and large NLO effects achieved by using simple azo chromophore</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=C2SC00834C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00834C, Edge Article&lt;/div&gt;&lt;div&gt;Wenbo Wu, Lijin Huang, Changfei Song, Gui Yu, Cheng Ye, Yunqi Liu, Jingui Qin, Qianqian Li, Zhen Li&lt;br/&gt;Large NLO effects, up to 246.0 pm V&lt;small&gt;&lt;sup&gt;-1&lt;/sup&gt;&lt;/small&gt;, were achieved by changing the topologies from normal dendrimers to global-like ones.&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/SC/~4/cayCvZsMA1I" height="1" width="1"/&gt;</description><a10:updated>2012-01-19T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Wenbo Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lijin Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Changfei Song</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gui Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cheng Ye</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yunqi Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jingui Qin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qianqian Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhen Li</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00834C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00885H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00885H</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/kUR40kabZY8/C2SC00885H</link><title>Potent inhibition of ice recrystallization by low molecular weight carbohydrate-based surfactants and hydrogelators</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00885H, Edge Article&lt;/div&gt;&lt;div&gt;Chantelle J. Capicciotti, Mathieu Leclere, Frederic A. Perras, David Bryce, Hilary Paulin, James Harden, Yun Liu, Robert N Ben&lt;br/&gt;Ice recrystallization inhibition (IRI) activity is a very desirable property for an effective cryoprotectant. This property was first observed in biological antifreezes (BAs), which cannot be utilized in cryopreservation due...&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/SC/~4/kUR40kabZY8" height="1" width="1"/&gt;</description><a10:updated>2012-02-06T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Chantelle J. Capicciotti</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mathieu Leclere</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Frederic A. Perras</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David Bryce</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hilary Paulin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">James Harden</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yun Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Robert N Ben</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00885H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00802E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00802E</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/3SF_pRdx8Ws/C2SC00802E</link><title>Di-cobalt(II) catalysts for the copolymerisation of CO2 and cyclohexene oxide: support for a dinuclear mechanism?</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=C2SC00802E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00802E, Edge Article&lt;/div&gt;&lt;div&gt;Michael R. Kember, Fabian Jutz, Antoine Buchard, Andrew J. P. White, Charlotte K. Williams&lt;br/&gt;Structure/reactivity and kinetic studies on a series of di-Co(&lt;small&gt;II&lt;/small&gt;) catalysts were both used to provide insight into the mechanism for the low pressure copolymerisation of CO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; and cyclohexene oxide.&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/SC/~4/3SF_pRdx8Ws" height="1" width="1"/&gt;</description><a10:updated>2012-02-06T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Michael R. Kember</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fabian Jutz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Antoine Buchard</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrew J. P. White</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Charlotte K. Williams</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00802E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01002J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01002J</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/aP4m3r9b2FI/C2SC01002J</link><title>Efficient gene delivery into cells by a surprisingly small three-armed peptide 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=C2SC01002J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01002J, Edge Article&lt;/div&gt;&lt;div&gt;Hannes Y. Kuchelmeister, Aljona Gutschmidt, Sarah Tillmann, Shirley Knauer, Carsten Schmuck&lt;br/&gt;The small, three-armed peptide ligand 1 and its divalent analogue 2 both bind to DNA with high affinities (1: &lt;i&gt;K ca.&lt;/i&gt; 10&lt;small&gt;&lt;sup&gt;7&lt;/sup&gt;&lt;/small&gt; M&lt;small&gt;&lt;sup&gt;-1&lt;/sup&gt;&lt;/small&gt;, 2: &lt;i&gt;K ca.&lt;/i&gt; 10&lt;small&gt;&lt;sup&gt;6&lt;/sup&gt;&lt;/small&gt; M&lt;small&gt;&lt;sup&gt;-1&lt;/sup&gt;&lt;/small&gt;) and transport DNA into human cells, but only 1 is able to efficiently transfect the cells as shown by the expression of GFP.&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/SC/~4/aP4m3r9b2FI" height="1" width="1"/&gt;</description><a10:updated>2012-01-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hannes Y. Kuchelmeister</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Aljona Gutschmidt</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sarah Tillmann</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shirley Knauer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Carsten Schmuck</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01002J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01042A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01042A</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/3jnn3xUBQtU/C2SC01042A</link><title>Metal-Free, Aerobic Ketooxygenation of Alkenes Using Hydroxamic Acids</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01042A, Edge Article&lt;/div&gt;&lt;div&gt;Valerie Anne Schmidt, Erik  Alexanian&lt;br/&gt;A metal-free, radical-mediated alkene ketooxygenation is described. This four-electron alkene oxidation delivers [small alpha]-oxyketones directly from simple alkenes with high levels of regio- and stereocontrol. The aerobic process capitalizes on the...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/SC/~4/3jnn3xUBQtU" height="1" width="1"/&gt;</description><a10:updated>2012-02-03T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Valerie Anne Schmidt</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Erik  Alexanian</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01042A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00997H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00997H</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/TNVmOW78GIU/C2SC00997H</link><title>Breathing molecular crystals: halogen- and hydrogen-bonded porous molecular crystals with solvent induced adaptation of the nanosized channels</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=C2SC00997H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00997H, Edge Article&lt;/div&gt;&lt;div&gt;Kari Raatikainen, Kari Rissanen&lt;br/&gt;Exceptionally strong (OC-)&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;N-IN halogen bonding (XB) in a combination with C[double bond, length as m-dash]OH-C hydrogen bonds (HB) between &lt;i&gt;N&lt;/i&gt;-iodosuccinimide (NIS) and hexamethylenetetramine (HMTA) yielded a series of molecular crystals possessing large 1D channels.&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/SC/~4/TNVmOW78GIU" height="1" width="1"/&gt;</description><a10:updated>2012-01-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Kari Raatikainen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kari Rissanen</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00997H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01003H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01003H</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/UspmQskBd6w/C2SC01003H</link><title>On the rational design of microwave-actuated organic 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=C2SC01003H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01003H, Edge Article&lt;/div&gt;&lt;div&gt;Michael R. Rosana, Yuchuan Tao, Albert E. Stiegman, Gregory B. Dudley&lt;br/&gt;Microwave-promoted reactivity of an ionic solute in a nonpolar solvent is shown to exceed temperature-based expectations.&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/SC/~4/UspmQskBd6w" height="1" width="1"/&gt;</description><a10:updated>2012-01-17T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Michael R. Rosana</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuchuan Tao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Albert E. Stiegman</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gregory B. Dudley</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01003H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00963C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00963C</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/e5OuMA0upOo/C2SC00963C</link><title>Highly enantioselective [4 + 2] annulations catalyzed by amino acid-based phosphines: Synthesis of functionalized cyclohexenes and 3-spirocyclohexene-2-oxindoles</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=C2SC00963C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00963C, Edge Article&lt;/div&gt;&lt;div&gt;Fangrui Zhong, Xiaoyu Han, Youqing Wang, Yixin Lu&lt;br/&gt;Highly enantioselective [4 + 2] annulation of activated alkenes with [small alpha]-substituted allenoates catalyzed by amino acid-based bifunctional phosphines has been developed for the first time.&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/SC/~4/e5OuMA0upOo" height="1" width="1"/&gt;</description><a10:updated>2012-01-10T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Fangrui Zhong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoyu Han</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Youqing Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yixin Lu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00963C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00920J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00920J</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/dTuYgyZUcOA/C2SC00920J</link><title>On the stereochemistry of acetylide additions to highly functionalized biphenylcarbaldehydes and multi-component cyclization of 1,n-diynes. Syntheses of dibenzocyclooctadiene lignans</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=C2SC00920J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00920J, Edge Article&lt;/div&gt;&lt;div&gt;Wei Gong, Ramakrishna Reddy Singidi, Judith C. Gallucci, T. V. RajanBabu&lt;br/&gt;Atropselective cyclization; but only with (&lt;i&gt;S&lt;small&gt;&lt;sub&gt;a&lt;/sub&gt;&lt;/small&gt;&lt;/i&gt;*,&lt;i&gt;S&lt;/i&gt;,*,&lt;i&gt;S&lt;/i&gt;*) starting propargyl ethers; no cyclization with diastereomer (&lt;i&gt;S&lt;small&gt;&lt;sub&gt;a&lt;/sub&gt;&lt;/small&gt;&lt;/i&gt;*,&lt;i&gt;R&lt;/i&gt;*,&lt;i&gt;S&lt;/i&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/SC/~4/dTuYgyZUcOA" height="1" width="1"/&gt;</description><a10:updated>2012-01-05T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Wei Gong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ramakrishna Reddy Singidi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Judith C. Gallucci</creator><creator xmlns="http://purl.org/dc/elements/1.1/">T. V. RajanBabu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00920J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00996J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00996J</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/ev3V75fR7DU/C2SC00996J</link><title>Cooperative self-assembly of squaraine dyes</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=C2SC00996J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00996J, Edge Article&lt;/div&gt;&lt;div&gt;Ulrich Mayerhoffer, Frank Wurthner&lt;br/&gt;We present the synthesis and cooperative self-assembly of a novel, highly soluble squaraine dye in organic solvents. The thermodynamics and the aggregate structure were studied by spectroscopic and microscopic methods.&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/SC/~4/ev3V75fR7DU" height="1" width="1"/&gt;</description><a10:updated>2012-02-02T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ulrich Mayerhoffer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Frank Wurthner</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00996J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01072K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01072K</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/62kKEfBsIHY/C2SC01072K</link><title>The Intramolecular Diels-Alder Reaction of Tryptamine-Derived Zincke Aldehydes Is a Stepwise Process</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01072K, Edge Article&lt;/div&gt;&lt;div&gt;Hung Pham, David Martin, Christopher D. Vanderwal, K Houk&lt;br/&gt;Computational studies show that the base-mediated intramolecular Diels-Alder of tryptamine-derived Zincke aldehydes, used as a key step in the synthesis of the Strychnos alkaloids norfluorocurarine and strychnine, proceeds via a...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/SC/~4/62kKEfBsIHY" height="1" width="1"/&gt;</description><a10:updated>2012-02-02T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hung Pham</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David Martin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christopher D. Vanderwal</creator><creator xmlns="http://purl.org/dc/elements/1.1/">K Houk</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01072K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00977C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00977C</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/jGYQatXUk_4/C2SC00977C</link><title>Development of a Robust Supramolecular Method to Prepare Well-defined Nanofibrils from Conjugated Molecules</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00977C, Edge Article&lt;/div&gt;&lt;div&gt;Tian Liangfei, Ruth Szilluweit, Roman Marty, Louis Bertschi, Mario Zerson, Eike-Christian Spitzner, Robert Magerle, Holger Frauenrath&lt;br/&gt;In order to produce materials with tailored structures and functions via supramolecular self-assembly of molecular precursors in a predictable fashion, it is necessary to develop 'supramolecular methods' based on structurally...&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/SC/~4/jGYQatXUk_4" height="1" width="1"/&gt;</description><a10:updated>2012-02-02T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Tian Liangfei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ruth Szilluweit</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Roman Marty</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Louis Bertschi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mario Zerson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Eike-Christian Spitzner</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Robert Magerle</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Holger Frauenrath</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00977C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00581F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00581F</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/2755RKp4csM/C2SC00581F</link><title>Lewis base-promoted carbon-carbon sp3-sp3 coupling reactions of [small alpha]-silyl silylethers</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=C2SC00581F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00581F, Edge Article&lt;/div&gt;&lt;div&gt;Jonathan A. Brekan, Dmitri Chernyak, Kolby L. White, Karl A. Scheidt&lt;br/&gt;An Umpolung d1 synthon-type reaction using [small alpha]-silyl silylethers and fluoride as the Lewis base has been developed.&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/SC/~4/2755RKp4csM" height="1" width="1"/&gt;</description><a10:updated>2012-02-02T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jonathan A. Brekan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dmitri Chernyak</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kolby L. White</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Karl A. Scheidt</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00581F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00888B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00888B</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/c74Zl3h29Fk/C2SC00888B</link><title>"Push effect" of sulfur coordination: promoting the breaking of C(sp2)-I bond by pincer thioimido-Pd(II) 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=C2SC00888B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00888B, Edge Article&lt;/div&gt;&lt;div&gt;Jing Liu, Yi Deng, Caitao Lin, Aiwen Lei&lt;br/&gt;Direct cleavage of an aryl-iodo bond by a well-defined Pd(&lt;small&gt;II&lt;/small&gt;) complex was achieved by assistance of sulfur coordination under neutral 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/SC/~4/c74Zl3h29Fk" height="1" width="1"/&gt;</description><a10:updated>2012-01-05T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jing Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yi Deng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Caitao Lin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Aiwen Lei</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00888B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01024K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01024K</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/lSzDX4M8T-c/C2SC01024K</link><title>Periodic trends in electron transport through extended metal atom chains: comparison of Ru3(dpa)4(NCS)2 with its first-row analogues.</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01024K, Edge Article&lt;/div&gt;&lt;div&gt;John E McGrady, Vihar Petkov Georgiev, Mohan Pilla janakiraman&lt;br/&gt;Density functional theory, in conjunction with non-equilibrium Green's functions, is used to reconcile the structural, magnetic and electron transport properties of a triruthenium extended metal atom chain, Ru3(dpa)4(NCS)2. The distinct...&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/SC/~4/lSzDX4M8T-c" height="1" width="1"/&gt;</description><a10:updated>2012-01-31T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">John E McGrady</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Vihar Petkov Georgiev</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mohan Pilla janakiraman</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01024K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00924B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00924B</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/bRYsMD0oSVs/C2SC00924B</link><title>Remarkably high temperature spin transition exhibited by two new metal-organic frameworks</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00924B, Edge Article&lt;/div&gt;&lt;div&gt;Ming-Liang Tong&lt;br/&gt;Highly satble two-dimensional coordination polymers, [FeII(L)2] (HL = 3-(2-pyridyl)-5-(3-pyridyl)-1,2,4-triazole (1) and 3-(3-methyl-2-pyridyl)-5-(3-pyridyl)-1,2,4-triazole (2), display well defined two-step spin crossover properties at unprecedented high temperatures, namely, Tc1 = 501 K, Tc2...&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/SC/~4/bRYsMD0oSVs" height="1" width="1"/&gt;</description><a10:updated>2012-01-31T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ming-Liang Tong</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00924B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00663D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00663D</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/zT3WimUgGR4/C2SC00663D</link><title>Synthetic Diversification of Natural Products: Semi-Synthesis and Evaluation of Triazole Jadomycins</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00663D, Edge Article&lt;/div&gt;&lt;div&gt;Stephanie N Dupuis, Andrew W Robertson, Thomas I Veinot, Susan MA Monroe, Susan E Douglas, Raymond T Syvitski, Kerry B Goralski, Sherri Ann McFarland, David L Jakeman&lt;br/&gt;Growth of Streptomyces venezuelae ISP5230 with O-propargyl-L-serine led to the efficient production of an alkyne-containing jadomycin. The installed alkyne functionality provided a uniquely reactive handle within the natural product and...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/SC/~4/zT3WimUgGR4" height="1" width="1"/&gt;</description><a10:updated>2012-01-31T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Stephanie N Dupuis</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrew W Robertson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Thomas I Veinot</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Susan MA Monroe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Susan E Douglas</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Raymond T Syvitski</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kerry B Goralski</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sherri Ann McFarland</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David L Jakeman</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00663D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00021K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00021K</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/7yhlhbNTLtE/C2SC00021K</link><title>Acid/Base Controlled Size Modulation of Capsular Phosphates, Hydroxide Encapsulation, Quantitative and Clean Extraction of Sulphate with Carbonate Capsules of a Tripodal Urea Receptor</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00021K, Edge Article&lt;/div&gt;&lt;div&gt;Pradyut Ghosh, Bidyut Akhuli, I Ravikumar&lt;br/&gt;A simple Tris-(2-aminoethyl) amine based pentafluorophenyl substituted tripodal urea receptor L has been extensively studied as a versatile receptor for various anions. Combined 1H-NMR, Isothermal Titration Calorimetric (ITC) and single...&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/SC/~4/7yhlhbNTLtE" height="1" width="1"/&gt;</description><a10:updated>2012-01-31T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Pradyut Ghosh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bidyut Akhuli</creator><creator xmlns="http://purl.org/dc/elements/1.1/">I Ravikumar</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00021K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00824F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00824F</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/8TTpvN0icf4/C2SC00824F</link><title>Largest discrete supertetrahedral clusters synthesized in ionic liquids</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=C2SC00824F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00824F, Edge Article&lt;/div&gt;&lt;div&gt;Wei-Wei Xiong, Jian-Rong Li, Bing Hu, Bin Tan, Ren-Fu Li, Xiao-Ying Huang&lt;br/&gt;Four discrete T5 cluster compounds with Cu-M-S constituents (M = In for compound 1, Ga for 2-4) have been synthesized in an ionic liquid. They represent the largest molecular clusters in a T&lt;i&gt;n&lt;/i&gt; series.&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/SC/~4/8TTpvN0icf4" height="1" width="1"/&gt;</description><a10:updated>2012-01-10T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Wei-Wei Xiong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jian-Rong Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bing Hu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bin Tan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ren-Fu Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiao-Ying Huang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00824F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01000C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01000C</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/gJSLFVsEIy8/C2SC01000C</link><title>Comparing the ultraviolet photostability of azole chromophores</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=C2SC01000C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01000C, Edge Article&lt;/div&gt;&lt;div&gt;Gareth M. Roberts, Craig A. Williams, Martin J. Paterson, Susanne Ullrich, Vasilios G. Stavros&lt;br/&gt;Using time-resolved velocity map ion imaging experiments the timescales for statistical H-atom elimination channels, following irradiation at 200 nm, in imidazole and pyrazole have been quantified.&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/SC/~4/gJSLFVsEIy8" height="1" width="1"/&gt;</description><a10:updated>2012-01-10T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Gareth M. Roberts</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Craig A. Williams</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Martin J. Paterson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Susanne Ullrich</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Vasilios G. Stavros</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01000C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00728B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00728B</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/9LbG7i6krfI/C2SC00728B</link><title>Heterometallic CuII/DyIII 1D chiral polymers: chirogenesis and exchange coupling of toroidal moments in trinuclear Dy3 single molecule magnets</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=C2SC00728B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00728B, Edge Article&lt;/div&gt;&lt;div&gt;Ghenadie Novitchi, Guillaume Pilet, Liviu Ungur, Victor V. Moshchalkov, Wolfgang Wernsdorfer, Liviu F. Chibotaru, Dominique Luneau, Annie K. Powell&lt;br/&gt;First observation of exchange coupling between the toroidal moments in 1D polymers built from Dy&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt; SMMs.&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/SC/~4/9LbG7i6krfI" height="1" width="1"/&gt;</description><a10:updated>2012-01-30T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ghenadie Novitchi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guillaume Pilet</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Liviu Ungur</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Victor V. Moshchalkov</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wolfgang Wernsdorfer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Liviu F. Chibotaru</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dominique Luneau</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Annie K. Powell</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00728B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00935H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00935H</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/3a7TC6ztg8w/C2SC00935H</link><title>Phosphorescent molecular tweezers based on alkynylplatinum(II) terpyridine system: turning on of NIR emission via heterologous PtM interactions (M = PtII, PdII, AuIII and AuI)</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=C2SC00935H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00935H, Edge Article&lt;/div&gt;&lt;div&gt;Yuya Tanaka, Keith Man-Chung Wong, Vivian Wing-Wah Yam&lt;br/&gt;Molecular tweezers of alkynylplatinum(&lt;small&gt;II&lt;/small&gt;) terpyridyl system can accommodate various metal complex guests, providing heterologous Pt(&lt;small&gt;II&lt;/small&gt;)M interactions, to give NIR emission.&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/SC/~4/3a7TC6ztg8w" height="1" width="1"/&gt;</description><a10:updated>2012-01-30T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yuya Tanaka</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Keith Man-Chung Wong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Vivian Wing-Wah Yam</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00935H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00971D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00971D</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/iRBpSTRQy1E/C2SC00971D</link><title>Au@Pt Dendrimer Encapsulated Nanoparticles as Model Electrocatalysts for Comparison of Experiment and Theory</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00971D, Edge Article&lt;/div&gt;&lt;div&gt;David F. Yancey, Liang Zhang, Richard M Crooks, Graeme Henkelman&lt;br/&gt;In this paper we report the electrochemical synthesis of core@shell dendrimer-encapsulated nanoparticles (DENs) consisting of cores containing 147 Au atoms (Au147) and Pt shells having ~54 or ~102 atoms (Au147@Ptn...&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/SC/~4/iRBpSTRQy1E" height="1" width="1"/&gt;</description><a10:updated>2012-01-30T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">David F. Yancey</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Liang Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Richard M Crooks</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Graeme Henkelman</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00971D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00953F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00953F</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/npR1w7WRSF4/C2SC00953F</link><title>Effect of bulky groups in ruthenium heteroleptic sensitizers on dye sensitized solar cell performance</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2SC00953F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00953F, Edge Article&lt;/div&gt;&lt;div&gt;Miguel Garcia-Iglesias, Laia Pelleja, Jun-Ho Yum, David Gonzalez-Rodriguez, Mohammad K. Nazeeruddin, Michael Gratzel, John N. Clifford, Emilio Palomares, Purificacion Vazquez, Tomas Torres&lt;br/&gt;Ruthenium heteroleptic sensitizers, with bulky groups on the ancillary bipyridine ligand, reduce aggregation and exhibit outstanding photocurrents and voltage in the absence of chenodeoxycholic acid.&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/SC/~4/npR1w7WRSF4" height="1" width="1"/&gt;</description><a10:updated>2012-01-27T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Miguel Garcia-Iglesias</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Laia Pelleja</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jun-Ho Yum</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David Gonzalez-Rodriguez</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mohammad K. Nazeeruddin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michael Gratzel</creator><creator xmlns="http://purl.org/dc/elements/1.1/">John N. Clifford</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Emilio Palomares</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Purificacion Vazquez</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tomas Torres</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00953F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01101H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01101H</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/baOfzuYLh0Q/C2SC01101H</link><title>Metallosupramolecular amphiphilic [small pi]-systems</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=C2SC01101H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC01101H, Minireview&lt;/div&gt;&lt;div&gt;Maria Jose Mayoral Munoz, Gustavo Fernandez&lt;br/&gt;Metallosupramolecular [small pi]-amphiphiles are emerging as a new class of adaptive materials with the ability to self-assemble into a wide variety of supramolecular structures through simultaneous [small pi]-[small pi], metallophilic and metal-ligand interactions.&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/SC/~4/baOfzuYLh0Q" height="1" width="1"/&gt;</description><a10:updated>2012-01-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Maria Jose Mayoral Munoz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gustavo Fernandez</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC01101H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00723A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00723A</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/QSkiJl1jwr8/C2SC00723A</link><title>Alloy tetrahexahedral Pd-Pt catalysts: enhancing significantly the catalytic activity by synergy effect of high-index facets and electronic structure</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=C2SC00723A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00723A, Edge Article&lt;/div&gt;&lt;div&gt;Yu-Jia Deng, Na Tian, Zhi-You Zhou, Rui Huang, Zi-Li Liu, Jing Xiao, Shi-Gang Sun&lt;br/&gt;Alloy tetrahexahedral Pd-Pt nanocrystals with high-index facets were synthesized, which exhibit very high catalytic activity for formic acid electrooxidation.&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/SC/~4/QSkiJl1jwr8" height="1" width="1"/&gt;</description><a10:updated>2012-01-05T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yu-Jia Deng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Na Tian</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhi-You Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rui Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zi-Li Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jing Xiao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shi-Gang Sun</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00723A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00770C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00770C</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/HWqcFqmb7H8/C2SC00770C</link><title>Functionalizing molecular wires: a tunable class of [small alpha],[small omega]-diphenyl-[small mu ],[small nu]-dicyano-oligoenes</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=C2SC00770C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00770C, Edge Article&lt;/div&gt;&lt;div&gt;Jeffrey S. Meisner, Danielle F. Sedbrook, Markrete Krikorian, Jun Chen, Aaron Sattler, Matthew E. Carnes, Christopher B. Murray, Michael Steigerwald, Colin Nuckolls&lt;br/&gt;A new method to synthesize cyano-substituted oligoenes with up to 13 all-&lt;i&gt;trans&lt;/i&gt; conjugated C[double bond, length as m-dash]C bonds has been developed and its utility shown in the synthesis of a wide variety of aryl-functionalized oligoenes.&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/SC/~4/HWqcFqmb7H8" height="1" width="1"/&gt;</description><a10:updated>2012-01-06T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jeffrey S. Meisner</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Danielle F. Sedbrook</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Markrete Krikorian</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jun Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Aaron Sattler</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Matthew E. Carnes</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christopher B. Murray</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michael Steigerwald</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Colin Nuckolls</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00770C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00950A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00950A</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/H1IAKJFDF8s/C2SC00950A</link><title>Catalytically active supramolecular porphyrin boxes: acceleration of the methanolysis of phosphate triesters via a combination of increased local nucleophilicity and reactant encapsulation</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00950A, Edge Article&lt;/div&gt;&lt;div&gt;Byungman Kang, Josh W Kurutz, Kyoung-Tae Youm, Ryan K Totten, J T Hupp, SonBinh Nguyen&lt;br/&gt;Box-like tetrakis(metalloporphyrin) supramolecular assemblies possessing Zn and Al metal sites can catalyze the methanolysis of phosphate triesters with a high rate enhancement, up to 430 times faster than the uncatalyzed...&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/SC/~4/H1IAKJFDF8s" height="1" width="1"/&gt;</description><a10:updated>2012-01-26T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Byungman Kang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Josh W Kurutz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kyoung-Tae Youm</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ryan K Totten</creator><creator xmlns="http://purl.org/dc/elements/1.1/">J T Hupp</creator><creator xmlns="http://purl.org/dc/elements/1.1/">SonBinh Nguyen</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00950A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00907B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00907B</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/RcdJfPLxcgQ/C2SC00907B</link><title>Synergistic catalysis: A powerful synthetic strategy for new reaction development</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=C2SC00907B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, &lt;b&gt;3&lt;/b&gt;,633-658&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00907B, Perspective&lt;/div&gt;&lt;div&gt;Anna E. Allen, David W. C. MacMillan&lt;br/&gt;Synergistic catalysis, the simultaneous activation of two reacting partners by discrete catalysts to enable new or elusive chemical transformations, is a valuable synthetic strategy that is growing in popularity. This review seeks to describe the new transformations that highlight the rapid onset of this powerful multi-catalysis concept.&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/SC/~4/RcdJfPLxcgQ" height="1" width="1"/&gt;</description><a10:updated>2012-01-25T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Anna E. Allen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David W. C. MacMillan</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00907B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00790H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00790H</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/nxZU_yDe5eQ/C2SC00790H</link><title>Synthetic lectin arrays for the detection and discrimination of cancer associated glycans and cell lines</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=C2SC00790H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00790H, Edge Article&lt;/div&gt;&lt;div&gt;Kevin L. Bicker, Jing Sun, Morgan Harrell, Yu Zhang, Maria M. Pena, Paul R. Thompson, John J. Lavigne&lt;br/&gt;The use of boronic acid functionalized synthetic lectins for the differentiation of cancer associated glycans and carcinogenic cell types&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/SC/~4/nxZU_yDe5eQ" height="1" width="1"/&gt;</description><a10:updated>2012-01-05T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Kevin L. Bicker</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jing Sun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Morgan Harrell</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yu Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Maria M. Pena</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Paul R. Thompson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">John J. Lavigne</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00790H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00923D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00923D</guid><link>http://feeds.rsc.org/~r/rss/SC/~3/ggqiZdAZY6w/C2SC00923D</link><title>Direct Oxidative Arylation of Secondary Alcohols with Arylsilanes via Rhodium-Catalyzed C-C Bond Cleavage</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2SC00923D, Edge Article&lt;/div&gt;&lt;div&gt;Zhang-Jie Shi, Kang Chen, Hu Li, Yang Li, Xi-Sha Zhang, Zhi-Quan Lei&lt;br/&gt;An unprecedented example of sequential pyridinyl directed C-C cleavage of secondary alcohols/ oxidative arylation with arylsilanes via Rh catalysis was reported. Preliminary studies indicated that the arylation initiated from Rh(III)-catalyzed...&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/SC/~4/ggqiZdAZY6w" height="1" width="1"/&gt;</description><a10:updated>2012-01-19T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Zhang-Jie Shi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kang Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hu Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yang Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xi-Sha Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhi-Quan Lei</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/SC/C2SC00923D</feedburner:origLink></item></channel></rss>

