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	<channel rdf:about="http://xlink.rsc.org/jumptojournal.cfm?journal_code=CC"><title>RSC - Chem. Commun. latest articles</title>
		<description>RSC - Chem. Commun. latest articles</description>
		<link>http://xlink.rsc.org/jumptojournal.cfm?journal_code=CC</link>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:language>en-gb</dc:language>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<prism:publicationName>Chem. Commun.</prism:publicationName>
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		<prism:issn>1359-7345</prism:issn><prism:eIssn>1364-548X</prism:eIssn><prism:publisher>The Royal Society of Chemistry</prism:publisher>
		<dc:creator>The Royal Society of Chemistry</dc:creator>
		<dc:description>Royal Society of Chemistry - Chem. Commun. latest articles</dc:description>
		<dc:title>RSC - Chem. Commun. latest articles </dc:title>
		<dc:source>http://www.rsc.org</dc:source>
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			<rdf:Seq><rdf:li rdf:resource="http://xlink.rsc.org/?DOI=b912326a&amp;RSS=1"/>
				<rdf:li rdf:resource="http://xlink.rsc.org/?DOI=b920865h&amp;RSS=1"/>
				<rdf:li rdf:resource="http://xlink.rsc.org/?DOI=b915825a&amp;RSS=1"/>
				<rdf:li rdf:resource="http://xlink.rsc.org/?DOI=b918444a&amp;RSS=1"/>
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				<rdf:li rdf:resource="http://xlink.rsc.org/?DOI=b917316a&amp;RSS=1"/>
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	<item rdf:about="http://xlink.rsc.org/?DOI=b912326a&amp;RSS=1"><title>Synthesis of nanostructured silicon carbide spheres from mesoporous C-SiO2 nanocomposites</title>
		<link>http://xlink.rsc.org/?DOI=b912326a&amp;RSS=1</link>
		<description>Nanostructured porous silicon carbide hollow spheres have been synthesized by phase separation in mesoporous silica-carbon nanocomposites at high temperatures and subsequent carbothermal reduction and crystallization.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b912326a-ga.gif"/&gt;
	&lt;/p&gt;Kun Wang, Huanting Wang, Yi-Bing Cheng &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Kun Wang, Chem. Commun., 2010, DOI: 10.1039/b912326a&lt;br/&gt;
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		<dc:title>Synthesis of nanostructured silicon carbide spheres from mesoporous C-SiO2 nanocomposites</dc:title>
		<dc:creator>Kun Wang</dc:creator>
		<dc:creator>Huanting Wang </dc:creator><dc:creator>Yi-Bing Cheng </dc:creator><dc:identifier>10.1039/b912326a</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b912326a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-24</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b912326a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b920865h&amp;RSS=1"><title>Directed evolution of gold nanoparticle delivery to cells</title>
		<link>http://xlink.rsc.org/?DOI=b920865h&amp;RSS=1</link>
		<description>A newly selected anti-receptor (anti-EGFR) aptamer was conjugated to gold nanoparticles via a facile hybridization method and was found to specifically direct the delivery of gold nanoparticles to cells expressing EGFR through receptor-mediated endocytosis.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b920865h-ga.gif"/&gt;
	&lt;/p&gt;Na Li, Timothy Larson, Hong H. Nguyen, Konstantin V. Sokolov, Andrew D. Ellington &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Na Li, Chem. Commun., 2010, DOI: 10.1039/b920865h&lt;br/&gt;
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		<dc:title>Directed evolution of gold nanoparticle delivery to cells</dc:title>
		<dc:creator>Na Li</dc:creator>
		<dc:creator>Timothy Larson </dc:creator><dc:creator>Hong H. Nguyen </dc:creator><dc:creator>Konstantin V. Sokolov </dc:creator><dc:creator>Andrew D. Ellington </dc:creator><dc:identifier>10.1039/b920865h</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b920865h</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-24</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b920865h</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b915825a&amp;RSS=1"><title>PPh3-catalyzed [2 + 2 + 2] and [4 + 2] annulations: synthesis of highly substituted 1,2-dihydropyridines (DHPs)</title>
		<link>http://xlink.rsc.org/?DOI=b915825a&amp;RSS=1</link>
		<description>PPh3-catalyzed [2 + 2 + 2] annulations between two units of an activated terminal alkyne and one unit of an aryl N-tosylimine have been developed to provide a synthetic method for highly substituted dihydropyridines.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b915825a-ga.gif"/&gt;
	&lt;/p&gt;Huimin Liu, Qiongmei Zhang, Limin Wang, Xiaofeng Tong &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Huimin Liu, Chem. Commun., 2010, DOI: 10.1039/b915825a&lt;br/&gt;
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		<dc:title>PPh3-catalyzed [2 + 2 + 2] and [4 + 2] annulations: synthesis of highly substituted 1,2-dihydropyridines (DHPs)</dc:title>
		<dc:creator>Huimin Liu</dc:creator>
		<dc:creator>Qiongmei Zhang </dc:creator><dc:creator>Limin Wang </dc:creator><dc:creator>Xiaofeng Tong </dc:creator><dc:identifier>10.1039/b915825a</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b915825a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-24</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b915825a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b918444a&amp;RSS=1"><title>Light wavelength-switchable photocatalytic reaction by gold nanoparticle-loaded titanium(iv) dioxide</title>
		<link>http://xlink.rsc.org/?DOI=b918444a&amp;RSS=1</link>
		<description>Surface plasmon resonance excitation of gold nanoparticles loaded on titanium(iv) dioxide (Au/TiO2) by visible light ([small lambda] &gt; 420 nm) has led to selective oxidation of thiol to disulfide, whereas the reaction is reversed by UV light irradiation ([small lambda] &gt; 300 nm).</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b918444a-ga.gif"/&gt;
	&lt;/p&gt;Shin-ichi Naya, Miwako Teranishi, Takeshi Isobe, Hiroaki Tada &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Shin-ichi Naya, Chem. Commun., 2010, DOI: 10.1039/b918444a&lt;br/&gt;
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		<dc:title>Light wavelength-switchable photocatalytic reaction by gold nanoparticle-loaded titanium(iv) dioxide</dc:title>
		<dc:creator>Shin-ichi Naya</dc:creator>
		<dc:creator>Miwako Teranishi </dc:creator><dc:creator>Takeshi Isobe </dc:creator><dc:creator>Hiroaki Tada </dc:creator><dc:identifier>10.1039/b918444a</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b918444a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-24</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b918444a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b917435d&amp;RSS=1"><title>Asymmetric synthesis of 2-substituted pyrrolidines by addition of Grignard reagents to [gamma]-chlorinated N-tert-butanesulfinyl imine</title>
		<link>http://xlink.rsc.org/?DOI=b917435d&amp;RSS=1</link>
		<description>A highly diastereoselective addition of various Grignard reagents to chiral [gamma]-chlorinated N-tert-butanesulfinyl imine resulting in the formation of 2-substituted pyrrolidines is reported.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b917435d-ga.gif"/&gt;
	&lt;/p&gt;Leleti Rajender Reddy, Mahavir Prashad &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Leleti Rajender Reddy, Chem. Commun., 2010, DOI: 10.1039/b917435d&lt;br/&gt;
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		<dc:title>Asymmetric synthesis of 2-substituted pyrrolidines by addition of Grignard reagents to [gamma]-chlorinated N-tert-butanesulfinyl imine</dc:title>
		<dc:creator>Leleti Rajender Reddy</dc:creator>
		<dc:creator>Mahavir Prashad </dc:creator><dc:identifier>10.1039/b917435d</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b917435d</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-24</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b917435d</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b917316a&amp;RSS=1"><title>Synthesis and characterization of diporphyrin sensitizers for dye-sensitized solar cells</title>
		<link>http://xlink.rsc.org/?DOI=b917316a&amp;RSS=1</link>
		<description>A dye-sensitized solar cell based on a novel meso-meso-linked porphyrin dimer exhibits a photovoltaic performance with conversion efficiency [small eta] = 5.23%.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b917316a-ga.gif"/&gt;
	&lt;/p&gt;Chi-Lun Mai, Wei-Kai Huang, Hsueh-Pei Lu, Cheng-Wei Lee, Chien-Lan Chiu, You-Ren Liang, Eric Wei-Guang Diau, Chen-Yu Yeh &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Chi-Lun Mai, Chem. Commun., 2010, DOI: 10.1039/b917316a&lt;br/&gt;
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		<dc:title>Synthesis and characterization of diporphyrin sensitizers for dye-sensitized solar cells</dc:title>
		<dc:creator>Chi-Lun Mai</dc:creator>
		<dc:creator>Wei-Kai Huang </dc:creator><dc:creator>Hsueh-Pei Lu </dc:creator><dc:creator>Cheng-Wei Lee </dc:creator><dc:creator>Chien-Lan Chiu </dc:creator><dc:creator>You-Ren Liang </dc:creator><dc:creator>Eric Wei-Guang Diau </dc:creator><dc:creator>Chen-Yu Yeh </dc:creator><dc:identifier>10.1039/b917316a</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b917316a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-24</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b917316a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b919902k&amp;RSS=1"><title>Highly enantioselective hydrogenation of [small alpha]-aryl-[small beta]-substituted acrylic acids catalyzed by Ir-SpinPHOX</title>
		<link>http://xlink.rsc.org/?DOI=b919902k&amp;RSS=1</link>
		<description>The enantioselective hydrogenation of a series of challenging substrates, [small alpha]-aryl-[small beta]-substituted acrylic acids, was realized with high efficiency and enantioselectivity (up to 96%) under the catalysis of Ir(i) complex of Spiro-based P,N ligand, SpinPHOX.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b919902k-ga.gif"/&gt;
	&lt;/p&gt;Yi Zhang, Zhaobin Han, Fuying Li, Kuiling Ding, Ao Zhang &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Yi Zhang, Chem. Commun., 2010, DOI: 10.1039/b919902k&lt;br/&gt;
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		<dc:title>Highly enantioselective hydrogenation of [small alpha]-aryl-[small beta]-substituted acrylic acids catalyzed by Ir-SpinPHOX</dc:title>
		<dc:creator>Yi Zhang</dc:creator>
		<dc:creator>Zhaobin Han </dc:creator><dc:creator>Fuying Li </dc:creator><dc:creator>Kuiling Ding </dc:creator><dc:creator>Ao Zhang </dc:creator><dc:identifier>10.1039/b919902k</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b919902k</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-24</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b919902k</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b916025f&amp;RSS=1"><title>Inducing synthesis of amorphous EuFePt nanorods and their comprehensive enhancement of magnetism, thermostability and photocatalysis</title>
		<link>http://xlink.rsc.org/?DOI=b916025f&amp;RSS=1</link>
		<description>The novel amorphous EuFePt nanorods are synthesized through inducing action, and exhibit the comprehensive enhancement effects on magnetism, thermostability and photocatalysis, suggesting applications in data storage, sensors, water photolysis, etc.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b916025f-ga.gif"/&gt;
	&lt;/p&gt;Ming Wen, Dan Yang, Qing-Sheng Wu, Ru-Ping Lu, Yuan-Zheng Zhu, Fan Zhang &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Ming Wen, Chem. Commun., 2010, DOI: 10.1039/b916025f&lt;br/&gt;
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		<dc:title>Inducing synthesis of amorphous EuFePt nanorods and their comprehensive enhancement of magnetism, thermostability and photocatalysis</dc:title>
		<dc:creator>Ming Wen</dc:creator>
		<dc:creator>Dan Yang </dc:creator><dc:creator>Qing-Sheng Wu </dc:creator><dc:creator>Ru-Ping Lu </dc:creator><dc:creator>Yuan-Zheng Zhu </dc:creator><dc:creator>Fan Zhang </dc:creator><dc:identifier>10.1039/b916025f</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b916025f</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-24</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b916025f</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b921113f&amp;RSS=1"><title>Organocatalytic asymmetric Povarov reactions with 2- and 3-vinylindoles</title>
		<link>http://xlink.rsc.org/?DOI=b921113f&amp;RSS=1</link>
		<description>The organocatalytic asymmetric Povarov reaction of N-arylimines with 2- and 3-vinylindoles has been developed. The peculiar reactivity of vinylindoles allowed the disclosure of versatile reaction manifolds for the preparation of highly enantioenriched indole derivatives.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b921113f-ga.gif"/&gt;
	&lt;/p&gt;Giulia Bergonzini, Lucia Gramigna, Andrea Mazzanti, Mariafrancesca Fochi, Luca Bernardi, Alfredo Ricci &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Giulia Bergonzini, Chem. Commun., 2010, DOI: 10.1039/b921113f&lt;br/&gt;
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		<dc:title>Organocatalytic asymmetric Povarov reactions with 2- and 3-vinylindoles</dc:title>
		<dc:creator>Giulia Bergonzini</dc:creator>
		<dc:creator>Lucia Gramigna </dc:creator><dc:creator>Andrea Mazzanti </dc:creator><dc:creator>Mariafrancesca Fochi </dc:creator><dc:creator>Luca Bernardi </dc:creator><dc:creator>Alfredo Ricci </dc:creator><dc:identifier>10.1039/b921113f</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b921113f</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-24</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b921113f</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b921237j&amp;RSS=1"><title>Total synthesis of a library of designed hybrids of the microtubule-stabilising anticancer agents taxol, discodermolide and dictyostatin</title>
		<link>http://xlink.rsc.org/?DOI=b921237j&amp;RSS=1</link>
		<description>A hybrid library of the marine natural products dictyostatin and discodermolide, incorporating the taxol or taxotere side chains, were synthesised; preliminary biological evaluation in the PANC-1 cancer cell line revealed significant antiproliferative activity.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b921237j-ga.gif"/&gt;
	&lt;/p&gt;Ian Paterson, Guy J. Naylor, Takeshi Fujita, Esther Guzman, Amy E. Wright &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Ian Paterson, Chem. Commun., 2010, DOI: 10.1039/b921237j&lt;br/&gt;
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		<dc:title>Total synthesis of a library of designed hybrids of the microtubule-stabilising anticancer agents taxol, discodermolide and dictyostatin</dc:title>
		<dc:creator>Ian Paterson</dc:creator>
		<dc:creator>Guy J. Naylor </dc:creator><dc:creator>Takeshi Fujita </dc:creator><dc:creator>Esther Guzman </dc:creator><dc:creator>Amy E. Wright </dc:creator><dc:identifier>10.1039/b921237j</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b921237j</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-24</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b921237j</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b920623j&amp;RSS=1"><title>A facile method for preparing one-molecule-thick free-standing organic nanosheets with a regular square shape</title>
		<link>http://xlink.rsc.org/?DOI=b920623j&amp;RSS=1</link>
		<description>A rapid and facile method was found to access one-molecule-thick (1.8 nm) free-standing organic nanosheets in a high yield with controllable size and shape by self-assembly of cucurbit[8]uril and small organic molecules.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b920623j-ga.gif"/&gt;
	&lt;/p&gt;Qi An, Qing Chen, Wei Zhu, Yan Li, Cheng-an Tao, Haowei Yang, Zhanping Li, Lijun Wan, He Tian, Guangtao Li &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Qi An, Chem. Commun., 2010, DOI: 10.1039/b920623j&lt;br/&gt;
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		<dc:title>A facile method for preparing one-molecule-thick free-standing organic nanosheets with a regular square shape</dc:title>
		<dc:creator>Qi An</dc:creator>
		<dc:creator>Qing Chen </dc:creator><dc:creator>Wei Zhu </dc:creator><dc:creator>Yan Li </dc:creator><dc:creator>Cheng-an Tao </dc:creator><dc:creator>Haowei Yang </dc:creator><dc:creator>Zhanping Li </dc:creator><dc:creator>Lijun Wan </dc:creator><dc:creator>He Tian </dc:creator><dc:creator>Guangtao Li </dc:creator><dc:identifier>10.1039/b920623j</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b920623j</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-23</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b920623j</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b916911c&amp;RSS=1"><title>A liposome-based nanostructure for aptamer directed delivery</title>
		<link>http://xlink.rsc.org/?DOI=b916911c&amp;RSS=1</link>
		<description>A therapeutic aptamer conjugated liposome drug delivery system was prepared.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b916911c-ga.gif"/&gt;
	&lt;/p&gt;Huaizhi Kang, Meghan B. O'Donoghue, Haipeng Liu, Weihong Tan &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Huaizhi Kang, Chem. Commun., 2010, DOI: 10.1039/b916911c&lt;br/&gt;
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		<dc:title>A liposome-based nanostructure for aptamer directed delivery</dc:title>
		<dc:creator>Huaizhi Kang</dc:creator>
		<dc:creator>Meghan B. O'Donoghue </dc:creator><dc:creator>Haipeng Liu </dc:creator><dc:creator>Weihong Tan </dc:creator><dc:identifier>10.1039/b916911c</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b916911c</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-23</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b916911c</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b918984j&amp;RSS=1"><title>Efficient protein renaturation using tunable hemifluorinated anionic surfactants as additives</title>
		<link>http://xlink.rsc.org/?DOI=b918984j&amp;RSS=1</link>
		<description>Anionic hemifluorinated surfactants provide high refolding yields for thermally and chemically denatured bovine carbonic anhydrase below their critical micelle concentration and can be easily displaced from the protein-surfactant complex by dialysis.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b918984j-ga.gif"/&gt;
	&lt;/p&gt;Rajni Singh, Robert A. Flowers, II &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Rajni Singh, Chem. Commun., 2010, DOI: 10.1039/b918984j&lt;br/&gt;
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		<dc:title>Efficient protein renaturation using tunable hemifluorinated anionic surfactants as additives</dc:title>
		<dc:creator>Rajni Singh</dc:creator>
		<dc:creator>Robert A. Flowers </dc:creator><dc:creator>II </dc:creator><dc:identifier>10.1039/b918984j</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b918984j</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-23</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b918984j</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b914083b&amp;RSS=1"><title>Decarbonylation of ethanol to methane, carbon monoxide and hydrogen by a [PNP]Ir complex</title>
		<link>http://xlink.rsc.org/?DOI=b914083b&amp;RSS=1</link>
		<description>Ethanol decarbonylation by the putative pincer complex [PNPPri]Ir(i) (PNPPri = [N{2-P(CHMe2)2-4-MeC6H3}2]-) furnishes trans-[PNPPri]Ir(H)(Me)(CO), which undergoes photochemical reductive elimination of methane.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b914083b-ga.gif"/&gt;
	&lt;/p&gt;Jonathan G. Melnick, Alexander T. Radosevich, Dino Villagran, Daniel G. Nocera &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Jonathan G. Melnick, Chem. Commun., 2010, DOI: 10.1039/b914083b&lt;br/&gt;
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		<dc:title>Decarbonylation of ethanol to methane, carbon monoxide and hydrogen by a [PNP]Ir complex</dc:title>
		<dc:creator>Jonathan G. Melnick</dc:creator>
		<dc:creator>Alexander T. Radosevich </dc:creator><dc:creator>Dino Villagran </dc:creator><dc:creator>Daniel G. Nocera </dc:creator><dc:identifier>10.1039/b914083b</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b914083b</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-23</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b914083b</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b923948k&amp;RSS=1"><title>Building on success: ChemComm - the next generation</title>
		<link>http://xlink.rsc.org/?DOI=b923948k&amp;RSS=1</link>
		<description>Happy New Year and welcome to the first issue of ChemComm for 2010. In this Editorial we reflect on an excellent 2009 and look forward to the future and further exciting developments for both ChemComm and RSC Publishing.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b923948k-ga.gif"/&gt;
	&lt;/p&gt;
(Editorial from Chem. Commun.)&lt;br/&gt;
Chem. Commun., 2010, DOI: 10.1039/b923948k&lt;br/&gt;
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		<dc:title>Building on success: ChemComm - the next generation</dc:title>
		<dc:creator>RSC</dc:creator>
		<dc:identifier>10.1039/b923948k</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b923948k</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-23</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b923948k</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b918989k&amp;RSS=1"><title>A zwitterionic zirconium complex that catalyzes hydroamination of aminoalkenes at room temperature</title>
		<link>http://xlink.rsc.org/?DOI=b918989k&amp;RSS=1</link>
		<description>A new mixed cyclopentadienyl-bis(oxazolinyl)borato zirconium(iv) complex catalyzes intramolecular hydroamination of aminoalkenes at room temperature.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b918989k-ga.gif"/&gt;
	&lt;/p&gt;Kuntal Manna, Arkady Ellern, Aaron D. Sadow &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Kuntal Manna, Chem. Commun., 2010, DOI: 10.1039/b918989k&lt;br/&gt;
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		<dc:title>A zwitterionic zirconium complex that catalyzes hydroamination of aminoalkenes at room temperature</dc:title>
		<dc:creator>Kuntal Manna</dc:creator>
		<dc:creator>Arkady Ellern </dc:creator><dc:creator>Aaron D. Sadow </dc:creator><dc:identifier>10.1039/b918989k</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b918989k</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-23</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b918989k</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b914977e&amp;RSS=1"><title>Hydrophobic ionic liquids with strongly coordinating anions</title>
		<link>http://xlink.rsc.org/?DOI=b914977e&amp;RSS=1</link>
		<description>"Ionic liquids containing the hexafluoroacetylacetonate anion are immiscible with water and they exhibit strong metal-complexing ability. These hydrophobic ionic liquids can be used for extraction and complexation of metal ions from an aqueous phase.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b914977e-ga.gif"/&gt;
	&lt;/p&gt;Hasan Mehdi, Koen Binnemans, Kristof Van Hecke, Luc Van Meervelt, Peter Nockemann &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Hasan Mehdi, Chem. Commun., 2010, DOI: 10.1039/b914977e&lt;br/&gt;
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		<dc:title>Hydrophobic ionic liquids with strongly coordinating anions</dc:title>
		<dc:creator>Hasan Mehdi</dc:creator>
		<dc:creator>Koen Binnemans </dc:creator><dc:creator>Kristof Van Hecke </dc:creator><dc:creator>Luc Van Meervelt </dc:creator><dc:creator>Peter Nockemann </dc:creator><dc:identifier>10.1039/b914977e</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b914977e</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-21</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b914977e</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b913067e&amp;RSS=1"><title>Stepwise and hysteretic sorption of N2, O2, CO2, and H2 gases in a porous metal-organic framework [Zn2(BPnDC)2(bpy)]</title>
		<link>http://xlink.rsc.org/?DOI=b913067e&amp;RSS=1</link>
		<description>A doubly interpenetrated porous metal-organic framework [Zn2(BPnDC)2(bpy)]n (SNU-9) exhibits three-step adsorption isotherms for N2 and O2 gases and two-step adsorption isotherms for H2 and CO2 gases, with hysteretic desorptions, while not adsorbing CH4 gas.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b913067e-ga.gif"/&gt;
	&lt;/p&gt;Hye Jeong Park, Myunghyun Paik Suh &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Hye Jeong Park, Chem. Commun., 2010, DOI: 10.1039/b913067e&lt;br/&gt;
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		<dc:title>Stepwise and hysteretic sorption of N2, O2, CO2, and H2 gases in a porous metal-organic framework [Zn2(BPnDC)2(bpy)]</dc:title>
		<dc:creator>Hye Jeong Park</dc:creator>
		<dc:creator>Myunghyun Paik Suh </dc:creator><dc:identifier>10.1039/b913067e</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b913067e</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-20</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b913067e</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b906808b&amp;RSS=1"><title>One-pot tandem 1,4-1,2-addition of phosphites to quinolines</title>
		<link>http://xlink.rsc.org/?DOI=b906808b&amp;RSS=1</link>
		<description>Phosphites were evaluated as nucleophiles for the addition to quinolines in acidic medium, allowing consecutive 1,4- and 1,2-addition breaking up the aromatic stabilization, leading to 2,4-diphosphono-1,2,3,4-tetrahydroquinolines in a one-step reaction. .</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b906808b-ga.gif"/&gt;
	&lt;/p&gt;Ann De Blieck, Kurt G. R. Masschelein, Frederic Dhaene, Ewa Rozycka-Sokolowska, Bernard Marciniak, Jozef Drabowicz, Christian V. Stevens &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Ann De Blieck, Chem. Commun., 2010, DOI: 10.1039/b906808b&lt;br/&gt;
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		<dc:title>One-pot tandem 1,4-1,2-addition of phosphites to quinolines</dc:title>
		<dc:creator>Ann De Blieck</dc:creator>
		<dc:creator>Kurt G. R. Masschelein </dc:creator><dc:creator>Frederic Dhaene </dc:creator><dc:creator>Ewa Rozycka-Sokolowska </dc:creator><dc:creator>Bernard Marciniak </dc:creator><dc:creator>Jozef Drabowicz </dc:creator><dc:creator>Christian V. Stevens </dc:creator><dc:identifier>10.1039/b906808b</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b906808b</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-20</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b906808b</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b919421e&amp;RSS=1"><title>Aminoclay: a permselective matrix to stabilize copper nanoparticles</title>
		<link>http://xlink.rsc.org/?DOI=b919421e&amp;RSS=1</link>
		<description>Air sensitive copper nanoparticles have been stabilized using a water soluble aminoclay matrix. The aminoclay shows remarkable permselective behaviour allowing only the ionic species to diffuse through it and react with copper nanoparticles.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b919421e-ga.gif"/&gt;
	&lt;/p&gt;K. K. R. Datta, C. Kulkarni, M. Eswaramoorthy &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
K. K. R. Datta, Chem. Commun., 2010, DOI: 10.1039/b919421e&lt;br/&gt;
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		<dc:title>Aminoclay: a permselective matrix to stabilize copper nanoparticles</dc:title>
		<dc:creator>K. K. R. Datta</dc:creator>
		<dc:creator>C. Kulkarni </dc:creator><dc:creator>M. Eswaramoorthy </dc:creator><dc:identifier>10.1039/b919421e</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b919421e</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-20</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b919421e</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b916224k&amp;RSS=1"><title>Degradable hollow spheres based on self-assembly inclusion</title>
		<link>http://xlink.rsc.org/?DOI=b916224k&amp;RSS=1</link>
		<description>Degradable hollow nanospheres are prepared by self-assembly of rod-coil Alg-g-PEG/[small alpha]-CD complexes in water, in which the rod-like segments were formed by inclusion between [small alpha]-CDs and grafted PEG chains and the coil-like segments were protonated alginate backbones.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b916224k-ga.gif"/&gt;
	&lt;/p&gt;Xian-Wei Meng, Jie Qin, Yan Liu, Min-Min Fan, Bang-Jing Li, Sheng Zhang, Xiao-Qi Yu &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Xian-Wei Meng, Chem. Commun., 2010, DOI: 10.1039/b916224k&lt;br/&gt;
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		<dc:title>Degradable hollow spheres based on self-assembly inclusion</dc:title>
		<dc:creator>Xian-Wei Meng</dc:creator>
		<dc:creator>Jie Qin </dc:creator><dc:creator>Yan Liu </dc:creator><dc:creator>Min-Min Fan </dc:creator><dc:creator>Bang-Jing Li </dc:creator><dc:creator>Sheng Zhang </dc:creator><dc:creator>Xiao-Qi Yu </dc:creator><dc:identifier>10.1039/b916224k</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b916224k</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-20</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b916224k</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b920676k&amp;RSS=1"><title>Sensitization of the NIR emission of Nd(iii) by the [small alpha]4 atropoisomer of a meso-tetraphenyl porphyrin bearing four 8-hydroxyquinolinylamide chelates</title>
		<link>http://xlink.rsc.org/?DOI=b920676k&amp;RSS=1</link>
		<description>A preorganised porphyrin-based ligand bearing four 8-hydroxyquinoline binds Nd(iii) and leads to its efficient NIR emission upon excitation in the visible region.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b920676k-ga.gif"/&gt;
	&lt;/p&gt;Fabrice Eckes, Veronique Bulach, Aurelie Guenet, Cristian A. Strassert, Luisa De Cola, Mir Wais Hosseini &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Fabrice Eckes, Chem. Commun., 2010, DOI: 10.1039/b920676k&lt;br/&gt;
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		<dc:title>Sensitization of the NIR emission of Nd(iii) by the [small alpha]4 atropoisomer of a meso-tetraphenyl porphyrin bearing four 8-hydroxyquinolinylamide chelates</dc:title>
		<dc:creator>Fabrice Eckes</dc:creator>
		<dc:creator>Veronique Bulach </dc:creator><dc:creator>Aurelie Guenet </dc:creator><dc:creator>Cristian A. Strassert </dc:creator><dc:creator>Luisa De Cola </dc:creator><dc:creator>Mir Wais Hosseini </dc:creator><dc:identifier>10.1039/b920676k</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b920676k</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-20</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b920676k</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b916483a&amp;RSS=1"><title>Nanoscale Si coating on the pore walls of SnO2 nanotube anode for Li rechargeable batteries</title>
		<link>http://xlink.rsc.org/?DOI=b916483a&amp;RSS=1</link>
		<description>We demonstrate that Si-coated SnO2 nanotubes could significantly improve the electrochemical properties of SnO2 nanotubes. The core-shell nanotubes with length of [similar]50 [small mu]m and diameter of 250-300 nm were prepared from a butyl-capped Si gel coating of an SnO2-loaded Al2O3 template.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b916483a-ga.gif"/&gt;
	&lt;/p&gt;Woo Jin Lee, Mi-Hee Park, Yong Wang, Jim Yang Lee, Jaephil Cho &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Woo Jin Lee, Chem. Commun., 2010, DOI: 10.1039/b916483a&lt;br/&gt;
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		<dc:title>Nanoscale Si coating on the pore walls of SnO2 nanotube anode for Li rechargeable batteries</dc:title>
		<dc:creator>Woo Jin Lee</dc:creator>
		<dc:creator>Mi-Hee Park </dc:creator><dc:creator>Yong Wang </dc:creator><dc:creator>Jim Yang Lee </dc:creator><dc:creator>Jaephil Cho </dc:creator><dc:identifier>10.1039/b916483a</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b916483a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-20</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b916483a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b918964e&amp;RSS=1"><title>Cellular uptake and binding of guanidine-modified phthalocyanines to KRAS/HRAS G-quadruplexes</title>
		<link>http://xlink.rsc.org/?DOI=b918964e&amp;RSS=1</link>
		<description>NIH 3T3 cells treated for 24 h with 2 [small mu]M DIGP and Zn-DIGP and analysed by confocal microscopy. Excitation = 633 nm, emission = 680-800 nm.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b918964e-ga.gif"/&gt;
	&lt;/p&gt;Alexandro Membrino, Manikandan Paramasivam, Susanna Cogoi, Jawad Alzeer, Nathan W. Luedtke, Luigi E. Xodo &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Alexandro Membrino, Chem. Commun., 2010, DOI: 10.1039/b918964e&lt;br/&gt;
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		<dc:title>Cellular uptake and binding of guanidine-modified phthalocyanines to KRAS/HRAS G-quadruplexes</dc:title>
		<dc:creator>Alexandro Membrino</dc:creator>
		<dc:creator>Manikandan Paramasivam </dc:creator><dc:creator>Susanna Cogoi </dc:creator><dc:creator>Jawad Alzeer </dc:creator><dc:creator>Nathan W. Luedtke </dc:creator><dc:creator>Luigi E. Xodo </dc:creator><dc:identifier>10.1039/b918964e</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b918964e</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-20</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b918964e</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b918881a&amp;RSS=1"><title>Hydrophobic chromophore cargo in micellar structures: a different strategy to sensitize lanthanide cations</title>
		<link>http://xlink.rsc.org/?DOI=b918881a&amp;RSS=1</link>
		<description>2,3-Naphthalimide is incorporated as a chromophore into a micellar assembly formed by an amphiphilic lanthanide chelate. The sensitizer to lanthanide energy transfer occurs between the two moieties without covalent linkage.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b918881a-ga.gif"/&gt;
	&lt;/p&gt;Celia S. Bonnet, Laurent Pellegatti, Frederic Buron, Chad M. Shade, Sandrine Villette, Vojtech Kubicek, Gerald Guillaumet, Franck Suzenet, Stephane Petoud, Eva Toth &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Celia S. Bonnet, Chem. Commun., 2010, DOI: 10.1039/b918881a&lt;br/&gt;
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		<dc:title>Hydrophobic chromophore cargo in micellar structures: a different strategy to sensitize lanthanide cations</dc:title>
		<dc:creator>Celia S. Bonnet</dc:creator>
		<dc:creator>Laurent Pellegatti </dc:creator><dc:creator>Frederic Buron </dc:creator><dc:creator>Chad M. Shade </dc:creator><dc:creator>Sandrine Villette </dc:creator><dc:creator>Vojtech Kubicek </dc:creator><dc:creator>Gerald Guillaumet </dc:creator><dc:creator>Franck Suzenet </dc:creator><dc:creator>Stephane Petoud </dc:creator><dc:creator>Eva Toth </dc:creator><dc:identifier>10.1039/b918881a</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b918881a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-20</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b918881a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b918433c&amp;RSS=1"><title>Conformations of a model protein revealed by an aggregating CuII porphyrin: sensing the difference</title>
		<link>http://xlink.rsc.org/?DOI=b918433c&amp;RSS=1</link>
		<description>A dicationic metalloporphyrin derivative acts as an extremely sensitive chiroptical probe for the major conformations of a model protein, binding as dimers on [small alpha]-helices or as aggregates on random coils, each mode displaying distinctive optical features.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b918433c-ga.gif"/&gt;
	&lt;/p&gt;Giovanna De Luca, Andrea Romeo, Luigi Monsu Scolaro, Robert F. Pasternack &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Giovanna De Luca, Chem. Commun., 2010, DOI: 10.1039/b918433c&lt;br/&gt;
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		<dc:title>Conformations of a model protein revealed by an aggregating CuII porphyrin: sensing the difference</dc:title>
		<dc:creator>Giovanna De Luca</dc:creator>
		<dc:creator>Andrea Romeo </dc:creator><dc:creator>Luigi Monsu Scolaro </dc:creator><dc:creator>Robert F. Pasternack </dc:creator><dc:identifier>10.1039/b918433c</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b918433c</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-19</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b918433c</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b914582f&amp;RSS=1"><title>Metal-organic replica of chiral natural material [small beta]-SnF2: an enantiopure binodal (3,5)-connected net based on triangular and trigonal bipyramidal coordination</title>
		<link>http://xlink.rsc.org/?DOI=b914582f&amp;RSS=1</link>
		<description>An enantiopure (3,5)-connected metal-organic framework, exhibiting a chiral [small beta]-SnF2 topology, is presented, which represents the first heterocoordinated chiral metal-organic analogue presently known with a natural material topology.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b914582f-ga.gif"/&gt;
	&lt;/p&gt;Jie Qin, Chao Qin, Xin-Long Wang, En-Bo Wang, Zhong-Min Su &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Jie Qin, Chem. Commun., 2010, DOI: 10.1039/b914582f&lt;br/&gt;
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		<dc:title>Metal-organic replica of chiral natural material [small beta]-SnF2: an enantiopure binodal (3,5)-connected net based on triangular and trigonal bipyramidal coordination</dc:title>
		<dc:creator>Jie Qin</dc:creator>
		<dc:creator>Chao Qin </dc:creator><dc:creator>Xin-Long Wang </dc:creator><dc:creator>En-Bo Wang </dc:creator><dc:creator>Zhong-Min Su </dc:creator><dc:identifier>10.1039/b914582f</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b914582f</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-19</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b914582f</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b918611e&amp;RSS=1"><title>Multimodal cell imaging by ruthenium polypyridyl labelled cell penetrating peptides</title>
		<link>http://xlink.rsc.org/?DOI=b918611e&amp;RSS=1</link>
		<description>The capacity of ruthenium polypyridyl complexes as probes for combined confocal luminescence and resonance Raman imaging, enabled by their large Stokes shift, is demonstrated for a novel membrane sensitive Ru(ii) polypyridyl peptide.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b918611e-ga.gif"/&gt;
	&lt;/p&gt;Lynda Cosgrave, Marc Devocelle, Robert J. Forster, Tia E. Keyes &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Lynda Cosgrave, Chem. Commun., 2010, DOI: 10.1039/b918611e&lt;br/&gt;
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		<dc:title>Multimodal cell imaging by ruthenium polypyridyl labelled cell penetrating peptides</dc:title>
		<dc:creator>Lynda Cosgrave</dc:creator>
		<dc:creator>Marc Devocelle </dc:creator><dc:creator>Robert J. Forster </dc:creator><dc:creator>Tia E. Keyes </dc:creator><dc:identifier>10.1039/b918611e</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b918611e</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-19</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b918611e</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b918923h&amp;RSS=1"><title>Bis(oxazolinyl)phenyl transition-metal complexes: asymmetric catalysis and some reactions of the metals</title>
		<link>http://xlink.rsc.org/?DOI=b918923h&amp;RSS=1</link>
		<description>Rh, Ru, Pt, Pd and Ni complexes binding bis(oxazolinyl)phenyl ligands have been prepared to showcase their highly potent activities for asymmetric catalysis in conjugate reductions, reductive aldol reactions, etc.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b918923h-ga.gif"/&gt;
	&lt;/p&gt;Hisao Nishiyama, Jun-ichi Ito &lt;br/&gt;
(Feature Article from Chem. Commun.)&lt;br/&gt;
Hisao Nishiyama, Chem. Commun., 2010, DOI: 10.1039/b918923h&lt;br/&gt;
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		<dc:title>Bis(oxazolinyl)phenyl transition-metal complexes: asymmetric catalysis and some reactions of the metals</dc:title>
		<dc:creator>Hisao Nishiyama</dc:creator>
		<dc:creator>Jun-ichi Ito </dc:creator><dc:identifier>10.1039/b918923h</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b918923h</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-19</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b918923h</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b914430g&amp;RSS=1"><title>Ionophore-gold nanoparticle conjugates for Ag+-selective sensors with nanomolar detection limit</title>
		<link>http://xlink.rsc.org/?DOI=b914430g&amp;RSS=1</link>
		<description>We report on the synthesis and trace analytical application of ionophore-gold nanoparticle conjugates as a basis of a new concept in confining ionophores to ion-selective membranes using inert nanoparticle carriers.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b914430g-ga.gif"/&gt;
	&lt;/p&gt;Gyula Jagerszki, Alajos Grun, Istvan Bitter, Klara Toth, Robert E. Gyurcsanyi &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Gyula Jagerszki, Chem. Commun., 2010, DOI: 10.1039/b914430g&lt;br/&gt;
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		<dc:title>Ionophore-gold nanoparticle conjugates for Ag+-selective sensors with nanomolar detection limit</dc:title>
		<dc:creator>Gyula Jagerszki</dc:creator>
		<dc:creator>Alajos Grun </dc:creator><dc:creator>Istvan Bitter </dc:creator><dc:creator>Klara Toth </dc:creator><dc:creator>Robert E. Gyurcsanyi </dc:creator><dc:identifier>10.1039/b914430g</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b914430g</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-19</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b914430g</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b921363e&amp;RSS=1"><title>Synthesis and photophysical properties of a hydrogen-bonded phthalocyanine-perylenediimide assembly</title>
		<link>http://xlink.rsc.org/?DOI=b921363e&amp;RSS=1</link>
		<description>A supramolecular Pc-PDI donor-acceptor array has been assembled by means of hydrogen bonding interactions using a melamine/perylenediimide motif. Photoexcitation of the PDI component affords transduction of singlet excited state energy to the energetically lower lying Pc.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b921363e-ga.gif"/&gt;
	&lt;/p&gt;Wolfgang Seitz, Angel J. Jimenez, Esther Carbonell, Bruno Grimm, M. Salome Rodriguez-Morgade, Dirk M. Guldi, Tomas Torres &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Wolfgang Seitz, Chem. Commun., 2010, DOI: 10.1039/b921363e&lt;br/&gt;
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		<dc:title>Synthesis and photophysical properties of a hydrogen-bonded phthalocyanine-perylenediimide assembly</dc:title>
		<dc:creator>Wolfgang Seitz</dc:creator>
		<dc:creator>Angel J. Jimenez </dc:creator><dc:creator>Esther Carbonell </dc:creator><dc:creator>Bruno Grimm </dc:creator><dc:creator>M. Salome Rodriguez-Morgade </dc:creator><dc:creator>Dirk M. Guldi </dc:creator><dc:creator>Tomas Torres </dc:creator><dc:identifier>10.1039/b921363e</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b921363e</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-19</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b921363e</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b920090h&amp;RSS=1"><title>Single and double substrate insertion into the Ti[double bond, length as m-dash]N[small alpha] bonds of terminal titanium hydrazides</title>
		<link>http://xlink.rsc.org/?DOI=b920090h&amp;RSS=1</link>
		<description>The first M[double bond, length as m-dash]N[small alpha] bond insertion reactions of any transition metal hydrazide complex are reported.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b920090h-ga.gif"/&gt;
	&lt;/p&gt;Pei-Jen Tiong, A. Daniel Schofield, Jonathan D. Selby, Ainara Nova, Eric Clot, Philip Mountford &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Pei-Jen Tiong, Chem. Commun., 2010, DOI: 10.1039/b920090h&lt;br/&gt;
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		<dc:title>Single and double substrate insertion into the Ti[double bond, length as m-dash]N[small alpha] bonds of terminal titanium hydrazides</dc:title>
		<dc:creator>Pei-Jen Tiong</dc:creator>
		<dc:creator>A. Daniel Schofield </dc:creator><dc:creator>Jonathan D. Selby </dc:creator><dc:creator>Ainara Nova </dc:creator><dc:creator>Eric Clot </dc:creator><dc:creator>Philip Mountford </dc:creator><dc:identifier>10.1039/b920090h</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b920090h</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-19</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b920090h</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b911777f&amp;RSS=1"><title>Highly ordered rectangular silver nanowire monolayers: water-assisted synthesis and galvanic replacement reaction with HAuCl4</title>
		<link>http://xlink.rsc.org/?DOI=b911777f&amp;RSS=1</link>
		<description>We demonstrate a simple water washing process for large-scale fabrication of highly ordered and aligned rectangular silver nanowire monolayers, which exhibit unique structure-dependent chemical reactivities for the galvanic replacement reaction with HAuCl4.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b911777f-ga.gif"/&gt;
	&lt;/p&gt;Yingpu Bi, Hongyan Hu, Gongxuan Lu &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Yingpu Bi, Chem. Commun., 2010, DOI: 10.1039/b911777f&lt;br/&gt;
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		<dc:title>Highly ordered rectangular silver nanowire monolayers: water-assisted synthesis and galvanic replacement reaction with HAuCl4</dc:title>
		<dc:creator>Yingpu Bi</dc:creator>
		<dc:creator>Hongyan Hu </dc:creator><dc:creator>Gongxuan Lu </dc:creator><dc:identifier>10.1039/b911777f</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b911777f</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-18</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b911777f</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b919279d&amp;RSS=1"><title>Trityl-nitroxide biradicals as unique molecular probes for the simultaneous measurement of redox status and oxygenation</title>
		<link>http://xlink.rsc.org/?DOI=b919279d&amp;RSS=1</link>
		<description>Novel trityl-nitroxide biradicals were synthesized and exhibited enhanced sensitivity and stability for rapid and simultaneous measurement of redox status and oxygenation by electron paramagnetic resonance spectroscopy.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b919279d-ga.gif"/&gt;
	&lt;/p&gt;Yangping Liu, Frederick A. Villamena, Antal Rockenbauer, Jay L. Zweier &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Yangping Liu, Chem. Commun., 2010, DOI: 10.1039/b919279d&lt;br/&gt;
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		<dc:title>Trityl-nitroxide biradicals as unique molecular probes for the simultaneous measurement of redox status and oxygenation</dc:title>
		<dc:creator>Yangping Liu</dc:creator>
		<dc:creator>Frederick A. Villamena </dc:creator><dc:creator>Antal Rockenbauer </dc:creator><dc:creator>Jay L. Zweier </dc:creator><dc:identifier>10.1039/b919279d</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b919279d</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-18</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b919279d</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b912769k&amp;RSS=1"><title>Meso-macro-porous monolithic Pt-Ni/Al2O3 catalysts used for miniaturizing preferential carbon monoxide oxidation reactor</title>
		<link>http://xlink.rsc.org/?DOI=b912769k&amp;RSS=1</link>
		<description>CO can be removed from H2-rich gases efficiently over meso-macroporous monolithic Pt-Ni/Al2O3 catalysts via preferential oxidation (PROX), and the miniaturization of CO-PROX reactor can be achieved.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b912769k-ga.gif"/&gt;
	&lt;/p&gt;Suhong Lu, Yuan Liu, Yaquan Wang &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Suhong Lu, Chem. Commun., 2010, DOI: 10.1039/b912769k&lt;br/&gt;
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		<dc:title>Meso-macro-porous monolithic Pt-Ni/Al2O3 catalysts used for miniaturizing preferential carbon monoxide oxidation reactor</dc:title>
		<dc:creator>Suhong Lu</dc:creator>
		<dc:creator>Yuan Liu </dc:creator><dc:creator>Yaquan Wang </dc:creator><dc:identifier>10.1039/b912769k</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b912769k</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-18</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b912769k</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b915712c&amp;RSS=1"><title>Photonic interaction between quantum dots and gold nanoparticles in discrete nanostructures through DNA directed self-assembly</title>
		<link>http://xlink.rsc.org/?DOI=b915712c&amp;RSS=1</link>
		<description>Discrete nanostructures of CdSe@ZnS QDs and Au NPs were prepared and the photonic interactions between the QDs and Au NPs were systematically investigated.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b915712c-ga.gif"/&gt;
	&lt;/p&gt;Qiangbin Wang, Haining Wang, Chenxiang Lin, Jaswinder Sharma, Shengli Zou, Yan Liu &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Qiangbin Wang, Chem. Commun., 2010, DOI: 10.1039/b915712c&lt;br/&gt;
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		<dc:title>Photonic interaction between quantum dots and gold nanoparticles in discrete nanostructures through DNA directed self-assembly</dc:title>
		<dc:creator>Qiangbin Wang</dc:creator>
		<dc:creator>Haining Wang </dc:creator><dc:creator>Chenxiang Lin </dc:creator><dc:creator>Jaswinder Sharma </dc:creator><dc:creator>Shengli Zou </dc:creator><dc:creator>Yan Liu </dc:creator><dc:identifier>10.1039/b915712c</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b915712c</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-18</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b915712c</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b920606j&amp;RSS=1"><title>Simultaneous production of p-tolualdehyde and hydrogen peroxide in photocatalytic oxygenation of p-xylene and reduction of oxygen with 9-mesityl-10-methylacridinium ion derivatives</title>
		<link>http://xlink.rsc.org/?DOI=b920606j&amp;RSS=1</link>
		<description>Photooxygenation of p-xylene by oxygen occurs efficiently under photoirradiation of mesitylacridinium in an O2-saturated acetonitrile solution to yield p-tolualdehyde and hydrogen peroxide.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b920606j-ga.gif"/&gt;
	&lt;/p&gt;Kei Ohkubo, Kentaro Mizushima, Ryosuke Iwata, Kazunori Souma, Nobuo Suzuki, Shunichi Fukuzumi &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Kei Ohkubo, Chem. Commun., 2010, DOI: 10.1039/b920606j&lt;br/&gt;
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		<dc:title>Simultaneous production of p-tolualdehyde and hydrogen peroxide in photocatalytic oxygenation of p-xylene and reduction of oxygen with 9-mesityl-10-methylacridinium ion derivatives</dc:title>
		<dc:creator>Kei Ohkubo</dc:creator>
		<dc:creator>Kentaro Mizushima </dc:creator><dc:creator>Ryosuke Iwata </dc:creator><dc:creator>Kazunori Souma </dc:creator><dc:creator>Nobuo Suzuki </dc:creator><dc:creator>Shunichi Fukuzumi </dc:creator><dc:identifier>10.1039/b920606j</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b920606j</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-18</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b920606j</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b914624e&amp;RSS=1"><title>The effect of atomic nitrogen on the C60 cage</title>
		<link>http://xlink.rsc.org/?DOI=b914624e&amp;RSS=1</link>
		<description>The investigation of N@C60 by laser flash photolysis demonstrates that the nonradiative relaxation from 3(N@C60)*, generated by photoirradiation, to its ground state is enhanced by N atom inside C60.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b914624e-ga.gif"/&gt;
	&lt;/p&gt;Hidefumi Nikawa, Yasuyuki Araki, Zdenek Slanina, Takahiro Tsuchiya, Takeshi Akasaka, Takehiko Wada, Osamu Ito, Klaus-Peter Dinse, Masafumi Ata, Tatsuhisa Kato, Shigeru Nagase &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Hidefumi Nikawa, Chem. Commun., 2010, DOI: 10.1039/b914624e&lt;br/&gt;
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		<dc:title>The effect of atomic nitrogen on the C60 cage</dc:title>
		<dc:creator>Hidefumi Nikawa</dc:creator>
		<dc:creator>Yasuyuki Araki </dc:creator><dc:creator>Zdenek Slanina </dc:creator><dc:creator>Takahiro Tsuchiya </dc:creator><dc:creator>Takeshi Akasaka </dc:creator><dc:creator>Takehiko Wada </dc:creator><dc:creator>Osamu Ito </dc:creator><dc:creator>Klaus-Peter Dinse </dc:creator><dc:creator>Masafumi Ata </dc:creator><dc:creator>Tatsuhisa Kato </dc:creator><dc:creator>Shigeru Nagase </dc:creator><dc:identifier>10.1039/b914624e</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b914624e</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-18</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b914624e</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b916822b&amp;RSS=1"><title>Hydrodeoxygenation of bio-derived phenols to hydrocarbons using Raney Ni and Nafion/SiO2 catalysts</title>
		<link>http://xlink.rsc.org/?DOI=b916822b&amp;RSS=1</link>
		<description>A simple, green, cost- and energy-efficient route for converting phenolic components in bio-oil to hydrocarbons and methanol has been developed, with nearly 100% yields. In the heterogeneous catalysts, Raney Ni acts as the hydrogenation catalysts and Nafion/SiO2 acts as the Bronsted solid acid for hydrolysis and dehydration.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b916822b-ga.gif"/&gt;
	&lt;/p&gt;Chen Zhao, Yuan Kou, Angeliki A. Lemonidou, Xuebing Li, Johannes A. Lercher &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Chen Zhao, Chem. Commun., 2010, DOI: 10.1039/b916822b&lt;br/&gt;
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		<dc:title>Hydrodeoxygenation of bio-derived phenols to hydrocarbons using Raney Ni and Nafion/SiO2 catalysts</dc:title>
		<dc:creator>Chen Zhao</dc:creator>
		<dc:creator>Yuan Kou </dc:creator><dc:creator>Angeliki A. Lemonidou </dc:creator><dc:creator>Xuebing Li </dc:creator><dc:creator>Johannes A. Lercher </dc:creator><dc:identifier>10.1039/b916822b</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b916822b</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-18</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b916822b</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b919815f&amp;RSS=1"><title>Chemical rescue of protein tyrosine phosphatase activity</title>
		<link>http://xlink.rsc.org/?DOI=b919815f&amp;RSS=1</link>
		<description>A rationally engineered protein tyrosine phosphatase mutant is potently and specifically activated by the addition of the biarsenical fluorescein derivative FlAsH.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b919815f-ga.gif"/&gt;
	&lt;/p&gt;Vincent L. Chen, Anthony C. Bishop &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Vincent L. Chen, Chem. Commun., 2010, DOI: 10.1039/b919815f&lt;br/&gt;
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		<dc:title>Chemical rescue of protein tyrosine phosphatase activity</dc:title>
		<dc:creator>Vincent L. Chen</dc:creator>
		<dc:creator>Anthony C. Bishop </dc:creator><dc:identifier>10.1039/b919815f</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b919815f</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-18</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b919815f</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b919607b&amp;RSS=1"><title>SERS aptasensor from nanorod-nanoparticle junction for protein detection</title>
		<link>http://xlink.rsc.org/?DOI=b919607b&amp;RSS=1</link>
		<description>A multicomponent nanostructure comprising of gold nanorod-nanoparticle junctions was fabricated. Experiments revealed that the strong electromagnetic coupling resonance at the nanorod-nanoparticle junction can be used to construct highly sensitive SERS aptasensors for protein detection.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b919607b-ga.gif"/&gt;
	&lt;/p&gt;Yuling Wang, Kyuwan Lee, Joseph Irudayaraj &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Yuling Wang, Chem. Commun., 2010, DOI: 10.1039/b919607b&lt;br/&gt;
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		<dc:title>SERS aptasensor from nanorod-nanoparticle junction for protein detection</dc:title>
		<dc:creator>Yuling Wang</dc:creator>
		<dc:creator>Kyuwan Lee </dc:creator><dc:creator>Joseph Irudayaraj </dc:creator><dc:identifier>10.1039/b919607b</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b919607b</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-18</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b919607b</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b919301d&amp;RSS=1"><title>Copper-catalysed bromoalkynylation of arynes</title>
		<link>http://xlink.rsc.org/?DOI=b919301d&amp;RSS=1</link>
		<description>Predominant insertion of two molar amounts of arynes into a C(sp)-Br bond of bromoalkynes readily proceeds in the presence of a substoichiometric amount of cupric bromide.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b919301d-ga.gif"/&gt;
	&lt;/p&gt;Takami Morishita, Hiroto Yoshida, Joji Ohshita &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Takami Morishita, Chem. Commun., 2010, DOI: 10.1039/b919301d&lt;br/&gt;
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		<dc:title>Copper-catalysed bromoalkynylation of arynes</dc:title>
		<dc:creator>Takami Morishita</dc:creator>
		<dc:creator>Hiroto Yoshida </dc:creator><dc:creator>Joji Ohshita </dc:creator><dc:identifier>10.1039/b919301d</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b919301d</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-18</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b919301d</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b919991h&amp;RSS=1"><title>Pd-catalyzed cascade carbopalladation-annulation reaction of 3-(2-iodobenzyl)-indoles into fused 6/5/7/6- and 6/5/5/6- heterocyclic systems</title>
		<link>http://xlink.rsc.org/?DOI=b919991h&amp;RSS=1</link>
		<description>Polycyclic indole structures, possessing fused seven-membered rings were efficiently synthesized via the Pd-catalyzed intramolecular carbopalladation-annulation of 3-(2-iodobenzyl)-indoles with alkynes.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b919991h-ga.gif"/&gt;
	&lt;/p&gt;Natalia Chernyak, David Tilly, Zhou Li, Vladimir Gevorgyan &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Natalia Chernyak, Chem. Commun., 2010, DOI: 10.1039/b919991h&lt;br/&gt;
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		<dc:title>Pd-catalyzed cascade carbopalladation-annulation reaction of 3-(2-iodobenzyl)-indoles into fused 6/5/7/6- and 6/5/5/6- heterocyclic systems</dc:title>
		<dc:creator>Natalia Chernyak</dc:creator>
		<dc:creator>David Tilly </dc:creator><dc:creator>Zhou Li </dc:creator><dc:creator>Vladimir Gevorgyan </dc:creator><dc:identifier>10.1039/b919991h</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b919991h</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-17</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b919991h</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b904135d&amp;RSS=1"><title>Spontaneous formation of vesicles in a catanionic association involving a head and tail functionalized amino-calix[6]arene</title>
		<link>http://xlink.rsc.org/?DOI=b904135d&amp;RSS=1</link>
		<description>Catanionic association of a calix[6]arene with a sugar-based surfactant forms spontaneous and stable unilamellar vesicles in aqueous solution.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b904135d-ga.gif"/&gt;
	&lt;/p&gt;Cecile Bize, Jean-Christophe Garrigues, Muriel Blanzat, Isabelle Rico-Lattes, Olivia Bistri, Benoit Colasson, Olivia Reinaud &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Cecile Bize, Chem. Commun., 2010, DOI: 10.1039/b904135d&lt;br/&gt;
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		<dc:title>Spontaneous formation of vesicles in a catanionic association involving a head and tail functionalized amino-calix[6]arene</dc:title>
		<dc:creator>Cecile Bize</dc:creator>
		<dc:creator>Jean-Christophe Garrigues </dc:creator><dc:creator>Muriel Blanzat </dc:creator><dc:creator>Isabelle Rico-Lattes </dc:creator><dc:creator>Olivia Bistri </dc:creator><dc:creator>Benoit Colasson </dc:creator><dc:creator>Olivia Reinaud </dc:creator><dc:identifier>10.1039/b904135d</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b904135d</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-17</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b904135d</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b920605a&amp;RSS=1"><title>Supramolecular photocatalysis by confinement-photodimerization of coumarins within cucurbit[8]urils</title>
		<link>http://xlink.rsc.org/?DOI=b920605a&amp;RSS=1</link>
		<description>Cucurbit[8]uril (as low as 10 mol%) acts as a supramolecular catalytic nanoreaction vessel and facilitates the photodimerization of coumarins leading to syn dimers. Saturation kinetics shows a sigmoidal dependence indicating a co-operative mechanism in the catalytic process.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b920605a-ga.gif"/&gt;
	&lt;/p&gt;Barry C. Pemberton, Nilotpal Barooah, D. K. Srivatsava, J. Sivaguru &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Barry C. Pemberton, Chem. Commun., 2010, DOI: 10.1039/b920605a&lt;br/&gt;
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		<dc:title>Supramolecular photocatalysis by confinement-photodimerization of coumarins within cucurbit[8]urils</dc:title>
		<dc:creator>Barry C. Pemberton</dc:creator>
		<dc:creator>Nilotpal Barooah </dc:creator><dc:creator>D. K. Srivatsava </dc:creator><dc:creator>J. Sivaguru </dc:creator><dc:identifier>10.1039/b920605a</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b920605a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-17</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b920605a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b910298a&amp;RSS=1"><title>Ortho-C-H borylation of benzoate esters with bis(pinacolato)diboron catalyzed by iridium-phosphine complexes</title>
		<link>http://xlink.rsc.org/?DOI=b910298a&amp;RSS=1</link>
		<description>Iridium complexes generated from [Ir(OMe)(COD)]2 and tris[3,5-bis(trifluoromethyl)phenyl]phosphine efficiently catalyzed the ortho-C-H borylation of benzoate esters with bis(pinacolato)diboron in octane at 80 [degree]C to produce the corresponding arylboronates in high yields.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b910298a-ga.gif"/&gt;
	&lt;/p&gt;Tatsuo Ishiyama, Hironori Isou, Takao Kikuchi, Norio Miyaura &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Tatsuo Ishiyama, Chem. Commun., 2010, DOI: 10.1039/b910298a&lt;br/&gt;
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		<dc:title>Ortho-C-H borylation of benzoate esters with bis(pinacolato)diboron catalyzed by iridium-phosphine complexes</dc:title>
		<dc:creator>Tatsuo Ishiyama</dc:creator>
		<dc:creator>Hironori Isou </dc:creator><dc:creator>Takao Kikuchi </dc:creator><dc:creator>Norio Miyaura </dc:creator><dc:identifier>10.1039/b910298a</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b910298a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-17</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b910298a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b919744c&amp;RSS=1"><title>Peptide-based activity-based probes (ABPs) for target-specific profiling of protein tyrosine phosphatases (PTPs)</title>
		<link>http://xlink.rsc.org/?DOI=b919744c&amp;RSS=1</link>
		<description>We report the synthesis of an unnatural amino acid for solid-phase synthesis of peptide-based probes suitable for activity-based profiling of endogenously expressed protein tyrosine phosphatases from mammalian cell lysates in a target specific manner.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b919744c-ga.gif"/&gt;
	&lt;/p&gt;Karunakaran A. Kalesh, Lay Pheng Tan, Kai Lu, Liqian Gao, Jigang Wang, Shao Q. Yao &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Karunakaran A. Kalesh, Chem. Commun., 2010, DOI: 10.1039/b919744c&lt;br/&gt;
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		<dc:title>Peptide-based activity-based probes (ABPs) for target-specific profiling of protein tyrosine phosphatases (PTPs)</dc:title>
		<dc:creator>Karunakaran A. Kalesh</dc:creator>
		<dc:creator>Lay Pheng Tan </dc:creator><dc:creator>Kai Lu </dc:creator><dc:creator>Liqian Gao </dc:creator><dc:creator>Jigang Wang </dc:creator><dc:creator>Shao Q. Yao </dc:creator><dc:identifier>10.1039/b919744c</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b919744c</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-17</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b919744c</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b920868b&amp;RSS=1"><title>A click chemistry based coordination polymer inside small heat shock protein</title>
		<link>http://xlink.rsc.org/?DOI=b920868b&amp;RSS=1</link>
		<description>A branched coordination polymer was formed within Hsp G41C using azide-alkyne click chemistry.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b920868b-ga.gif"/&gt;
	&lt;/p&gt;Janice Lucon, Md Joynal Abedin, Masaki Uchida, Lars Liepold, Craig C. Jolley, Mark Young, Trevor Douglas &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Janice Lucon, Chem. Commun., 2010, DOI: 10.1039/b920868b&lt;br/&gt;
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		<dc:title>A click chemistry based coordination polymer inside small heat shock protein</dc:title>
		<dc:creator>Janice Lucon</dc:creator>
		<dc:creator>Md Joynal Abedin </dc:creator><dc:creator>Masaki Uchida </dc:creator><dc:creator>Lars Liepold </dc:creator><dc:creator>Craig C. Jolley </dc:creator><dc:creator>Mark Young </dc:creator><dc:creator>Trevor Douglas </dc:creator><dc:identifier>10.1039/b920868b</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b920868b</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-17</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b920868b</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b916304b&amp;RSS=1"><title>Electrochemical analysis of two analytes based on a dual-functional aptamer DNA sequence</title>
		<link>http://xlink.rsc.org/?DOI=b916304b&amp;RSS=1</link>
		<description>A multifunctional electrochemical strategy based on a dual-aptamer for the detection of adenosine and thrombin in one-pot has been developed, by coupling the enhancement of bio-bar-code technology and anodic stripping voltammetry (ASV). Limits of detection are as low as 8.8 [times] 10-12 M and 7.6 [times] 10-13 M for adenosine and thrombin, respectively.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b916304b-ga.gif"/&gt;
	&lt;/p&gt;Xuemei Li, Jinming Liu, Shusheng Zhang &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Xuemei Li, Chem. Commun., 2010, DOI: 10.1039/b916304b&lt;br/&gt;
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		<dc:title>Electrochemical analysis of two analytes based on a dual-functional aptamer DNA sequence</dc:title>
		<dc:creator>Xuemei Li</dc:creator>
		<dc:creator>Jinming Liu </dc:creator><dc:creator>Shusheng Zhang </dc:creator><dc:identifier>10.1039/b916304b</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b916304b</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-17</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b916304b</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b919044a&amp;RSS=1"><title>Facile EG/ionic liquid interfacial synthesis of uniform RE3+ doped NaYF4 nanocubes</title>
		<link>http://xlink.rsc.org/?DOI=b919044a&amp;RSS=1</link>
		<description>A facile EG/ionic liquid interfacial synthesis route has been developed to fabricate uniform RE3+ doped NaYF4 nanocubes. Multicolor upconversion luminescence is achieved in the nanocubes by tuning the dopants and dopant concentration.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b919044a-ga.gif"/&gt;
	&lt;/p&gt;Chao Zhang, Ji Chen &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Chao Zhang, Chem. Commun., 2010, DOI: 10.1039/b919044a&lt;br/&gt;
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		<dc:title>Facile EG/ionic liquid interfacial synthesis of uniform RE3+ doped NaYF4 nanocubes</dc:title>
		<dc:creator>Chao Zhang</dc:creator>
		<dc:creator>Ji Chen </dc:creator><dc:identifier>10.1039/b919044a</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b919044a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-17</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b919044a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b918505d&amp;RSS=1"><title>Synthesis of monodispersed nanoparticles functionalized carbon nanotubes in plasma-ionic liquid interfacial fields</title>
		<link>http://xlink.rsc.org/?DOI=b918505d&amp;RSS=1</link>
		<description>High-density and monodispersed metal nanoparticles intercalated into and encapsulated inside single-walled and double-walled carbon nanotubes are synthesized using a plasma technique combined with the introduction of ionic liquids.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b918505d-ga.gif"/&gt;
	&lt;/p&gt;Kazuhiko Baba, Toshiro Kaneko, Rikizo Hatakeyama, Kenichi Motomiya, Kazuyuki Tohji &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Kazuhiko Baba, Chem. Commun., 2010, DOI: 10.1039/b918505d&lt;br/&gt;
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&lt;br/&gt;&lt;a href='http://obofoundry.org/' target="'_BLANK'"&gt;Ontology Terms:&lt;/a&gt;
	catalyst; carbon nanotube; single-walled carbon nanotube; double-walled carbon nanotube; gold nanoparticle; nanoparticle; transmission electron microscopy; energy-dispersive X-ray emission spectroscopy; transmission electron microscope; sonication; synthesis method; transmission electron micrograph; supercritical fluid method; energy-dispersive X-ray spectrum; palladium nanoparticle; electrode
&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry</content:encoded>
		<dc:title>Synthesis of monodispersed nanoparticles functionalized carbon nanotubes in plasma-ionic liquid interfacial fields</dc:title>
		<dc:creator>Kazuhiko Baba</dc:creator>
		<dc:creator>Toshiro Kaneko </dc:creator><dc:creator>Rikizo Hatakeyama </dc:creator><dc:creator>Kenichi Motomiya </dc:creator><dc:creator>Kazuyuki Tohji </dc:creator><dc:identifier>10.1039/b918505d</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b918505d</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-17</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b918505d</dc:identifier>
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				<rdf:li><content:item rdf:about="http://purl.org/obo/owl/CHEBI#CHEBI_50595"/>
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				<rdf:li><content:item rdf:about="http://purl.org/obo/owl/CHEBI#CHEBI_50797"/>
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				<rdf:li><content:item rdf:about="http://purl.org/obo/owl/CHEBI#CHEBI_50825"/>
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				<rdf:li><content:item rdf:about="http://purl.org/obo/owl/CHEBI#CHEBI_50803"/>
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				<rdf:li><content:item rdf:about="http://www.rsc.org/ontologies/CMO_OWL.owl#CMO_0001707"/>
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				<rdf:li><content:item rdf:about="http://www.rsc.org/ontologies/CMO_OWL.owl#CMO_0001301"/>
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				<rdf:li><content:item rdf:about="http://www.rsc.org/ontologies/CMO_OWL.owl#CMO_0001802"/>
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				<rdf:li><content:item rdf:about="http://www.rsc.org/ontologies/CMO_OWL.owl#CMO_0001904"/>
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				<rdf:li><content:item rdf:about="http://www.rsc.org/ontologies/CMO_OWL.owl#CMO_0002227"/>
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				<rdf:li><content:item rdf:about="http://purl.org/obo/owl/CHEBI#CHEBI_52853"/>
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				<rdf:li><content:item rdf:about="http://www.rsc.org/ontologies/CMO_OWL.owl#CMO_0002344"/>
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	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b915589a&amp;RSS=1"><title>Increasing the hydrophobicity and electrospray response of glycans through derivatization with novel cationic hydrazides</title>
		<link>http://xlink.rsc.org/?DOI=b915589a&amp;RSS=1</link>
		<description>Novel reagents are utilized to increase the hydrophobicity of glycans yielding an increase in electrospray response and a decrease in retention time under hydrophilic interaction liquid chromatography conditions.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b915589a-ga.gif"/&gt;
	&lt;/p&gt;Michael S. Bereman, Daniel L. Comins, David C. Muddiman &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Michael S. Bereman, Chem. Commun., 2010, DOI: 10.1039/b915589a&lt;br/&gt;
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&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry</content:encoded>
		<dc:title>Increasing the hydrophobicity and electrospray response of glycans through derivatization with novel cationic hydrazides</dc:title>
		<dc:creator>Michael S. Bereman</dc:creator>
		<dc:creator>Daniel L. Comins </dc:creator><dc:creator>David C. Muddiman </dc:creator><dc:identifier>10.1039/b915589a</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b915589a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-17</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b915589a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b921000h&amp;RSS=1"><title>Total synthesis of largamide H</title>
		<link>http://xlink.rsc.org/?DOI=b921000h&amp;RSS=1</link>
		<description>The first total synthesis of largamide H has been completed, utilising the oxidative elimination reaction of enantiomerically pure 2-amino-3-(phenylselenyl)butanoic acid residues to stereospecifically install both (Z)-and (E)-2,3-dehydro-2-aminobutanoic moieties.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b921000h-ga.gif"/&gt;
	&lt;/p&gt;Shuo Liang, Zhengshuang Xu, Tao Ye &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Shuo Liang, Chem. Commun., 2010, DOI: 10.1039/b921000h&lt;br/&gt;
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&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry</content:encoded>
		<dc:title>Total synthesis of largamide H</dc:title>
		<dc:creator>Shuo Liang</dc:creator>
		<dc:creator>Zhengshuang Xu </dc:creator><dc:creator>Tao Ye </dc:creator><dc:identifier>10.1039/b921000h</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b921000h</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-16</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b921000h</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b913879j&amp;RSS=1"><title>Ionogels as drug delivery system: one-step sol-gel synthesis using imidazolium ibuprofenate ionic liquid</title>
		<link>http://xlink.rsc.org/?DOI=b913879j&amp;RSS=1</link>
		<description>Ionogels containing imidazolium ibuprofenate synthesized by a one-step sol-gel synthesis have been shown to be an efficient drug delivery system with kinetics controlled by the nature of the silica wall.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b913879j-ga.gif"/&gt;
	&lt;/p&gt;Lydie Viau, Corine Tourne-Peteilh, Jean-Marie Devoisselle, Andre Vioux &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Lydie Viau, Chem. Commun., 2010, DOI: 10.1039/b913879j&lt;br/&gt;
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&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry</content:encoded>
		<dc:title>Ionogels as drug delivery system: one-step sol-gel synthesis using imidazolium ibuprofenate ionic liquid</dc:title>
		<dc:creator>Lydie Viau</dc:creator>
		<dc:creator>Corine Tourne-Peteilh </dc:creator><dc:creator>Jean-Marie Devoisselle </dc:creator><dc:creator>Andre Vioux </dc:creator><dc:identifier>10.1039/b913879j</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b913879j</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-16</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b913879j</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b917016b&amp;RSS=1"><title>Can nitrones functionalize carbon nanotubes?</title>
		<link>http://xlink.rsc.org/?DOI=b917016b&amp;RSS=1</link>
		<description>Functionalization of Multi-Walled Carbon Nanotubes by the 1,3-dipolar cycloaddition of a cyclic nitrone yields material with great solubility in DMF, preferentially occurring at the defects of the MWCNT sp2 network.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b917016b-ga.gif"/&gt;
	&lt;/p&gt;Giacomo Ghini, Lapo Luconi, Andrea Rossin, Claudio Bianchini, Giuliano Giambastiani, Stefano Cicchi, Luisa Lascialfari, Alberto Brandi, Alessandra Giannasi &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Giacomo Ghini, Chem. Commun., 2010, DOI: 10.1039/b917016b&lt;br/&gt;
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&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry</content:encoded>
		<dc:title>Can nitrones functionalize carbon nanotubes?</dc:title>
		<dc:creator>Giacomo Ghini</dc:creator>
		<dc:creator>Lapo Luconi </dc:creator><dc:creator>Andrea Rossin </dc:creator><dc:creator>Claudio Bianchini </dc:creator><dc:creator>Giuliano Giambastiani </dc:creator><dc:creator>Stefano Cicchi </dc:creator><dc:creator>Luisa Lascialfari </dc:creator><dc:creator>Alberto Brandi </dc:creator><dc:creator>Alessandra Giannasi </dc:creator><dc:identifier>10.1039/b917016b</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b917016b</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-16</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b917016b</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b915871e&amp;RSS=1"><title>Addressable electrochemiluminescence detection system based on redox-cycling of Ru(bpy)32+</title>
		<link>http://xlink.rsc.org/?DOI=b915871e&amp;RSS=1</link>
		<description>An addressable ECL detection system based on redox-cycling of (Ru(bpy)32+ is developed. By changing the column or row electrodes addressed, the ECL at each address point can be detected separately.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b915871e-ga.gif"/&gt;
	&lt;/p&gt;Zhenyu Lin, Kosuke Ino, Hitoshi Shiku, Tomokazu Matsue, Guonan Chen &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Zhenyu Lin, Chem. Commun., 2010, DOI: 10.1039/b915871e&lt;br/&gt;
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&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry</content:encoded>
		<dc:title>Addressable electrochemiluminescence detection system based on redox-cycling of Ru(bpy)32+</dc:title>
		<dc:creator>Zhenyu Lin</dc:creator>
		<dc:creator>Kosuke Ino </dc:creator><dc:creator>Hitoshi Shiku </dc:creator><dc:creator>Tomokazu Matsue </dc:creator><dc:creator>Guonan Chen </dc:creator><dc:identifier>10.1039/b915871e</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b915871e</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-16</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b915871e</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b915650j&amp;RSS=1"><title>A novel coral-like porous SnO2 hollow architecture: biomimetic swallowing growth mechanism and enhanced photovoltaic property for dye-sensitized solar cell application</title>
		<link>http://xlink.rsc.org/?DOI=b915650j&amp;RSS=1</link>
		<description>A unique coral-like porous SnO2 hollow architecture with enhanced photovoltaic property for dye-sensitized solar cell application was prepared, and a biomimetic swallowing growth mechanism for the formation of the special structure was also proposed for the first time.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b915650j-ga.gif"/&gt;
	&lt;/p&gt;Jinyun Liu, Tao Luo, Sitaramanjaneya Mouli T, Fanli Meng, Bai Sun, Minqiang Li, Jinhuai Liu &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Jinyun Liu, Chem. Commun., 2010, DOI: 10.1039/b915650j&lt;br/&gt;
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		<dc:title>A novel coral-like porous SnO2 hollow architecture: biomimetic swallowing growth mechanism and enhanced photovoltaic property for dye-sensitized solar cell application</dc:title>
		<dc:creator>Jinyun Liu</dc:creator>
		<dc:creator>Tao Luo </dc:creator><dc:creator>Sitaramanjaneya Mouli T </dc:creator><dc:creator>Fanli Meng </dc:creator><dc:creator>Bai Sun </dc:creator><dc:creator>Minqiang Li </dc:creator><dc:creator>Jinhuai Liu </dc:creator><dc:identifier>10.1039/b915650j</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b915650j</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-16</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b915650j</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b919353g&amp;RSS=1"><title>Immobilization of calix[4]arene-based glycoclusters on TiO2 nanoparticles via click Cu(i)-catalyzed azide-alkyne coupling</title>
		<link>http://xlink.rsc.org/?DOI=b919353g&amp;RSS=1</link>
		<description>The first preparation of TiO2 nanoparticles coated by a monolayer of calixarene-based galactoside or sialoside clusters.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b919353g-ga.gif"/&gt;
	&lt;/p&gt;Lisa Moni, Stefano Rossetti, Marco Scoponi, Alberto Marra, Alessandro Dondoni &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Lisa Moni, Chem. Commun., 2010, DOI: 10.1039/b919353g&lt;br/&gt;
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&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry</content:encoded>
		<dc:title>Immobilization of calix[4]arene-based glycoclusters on TiO2 nanoparticles via click Cu(i)-catalyzed azide-alkyne coupling</dc:title>
		<dc:creator>Lisa Moni</dc:creator>
		<dc:creator>Stefano Rossetti </dc:creator><dc:creator>Marco Scoponi </dc:creator><dc:creator>Alberto Marra </dc:creator><dc:creator>Alessandro Dondoni </dc:creator><dc:identifier>10.1039/b919353g</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b919353g</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-16</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b919353g</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b920037a&amp;RSS=1"><title>Facile scalable synthesis of magnetite nanocrystals embedded in carbon matrix as superior anode materials for lithium-ion batteries</title>
		<link>http://xlink.rsc.org/?DOI=b920037a&amp;RSS=1</link>
		<description>A simple and scalable process was developed for the synthesis of highly crystalline magnetite nanocrystals embedded in a carbon matrix; the resulting nanocomposite showed a very high specific capacity of 863 mA hg-1 in the initial cycle and high capacity retention of 90% after 30 cycles.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b920037a-ga.gif"/&gt;
	&lt;/p&gt;Yuanzhe Piao, Hyun Sik Kim, Yung-Eun Sung, Taeghwan Hyeon &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Yuanzhe Piao, Chem. Commun., 2010, DOI: 10.1039/b920037a&lt;br/&gt;
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&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry</content:encoded>
		<dc:title>Facile scalable synthesis of magnetite nanocrystals embedded in carbon matrix as superior anode materials for lithium-ion batteries</dc:title>
		<dc:creator>Yuanzhe Piao</dc:creator>
		<dc:creator>Hyun Sik Kim </dc:creator><dc:creator>Yung-Eun Sung </dc:creator><dc:creator>Taeghwan Hyeon </dc:creator><dc:identifier>10.1039/b920037a</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b920037a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-16</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b920037a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b919971n&amp;RSS=1"><title>Facile synthesis of robust and biocompatible gold nanoparticles</title>
		<link>http://xlink.rsc.org/?DOI=b919971n&amp;RSS=1</link>
		<description>Gold nanoparticles (AuNPs) were prepared by employing dextran as a reducing agent and surface coating material. Colloidal stability, biocompatibility, and capability of bioconjugation will make the AuNPs readily applicable in biology.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b919971n-ga.gif"/&gt;
	&lt;/p&gt;Hongje Jang, Young-Kwan Kim, Soo-Ryoon Ryoo, Mi-Hee Kim, Dal-Hee Min &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Hongje Jang, Chem. Commun., 2010, DOI: 10.1039/b919971n&lt;br/&gt;
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&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry</content:encoded>
		<dc:title>Facile synthesis of robust and biocompatible gold nanoparticles</dc:title>
		<dc:creator>Hongje Jang</dc:creator>
		<dc:creator>Young-Kwan Kim </dc:creator><dc:creator>Soo-Ryoon Ryoo </dc:creator><dc:creator>Mi-Hee Kim </dc:creator><dc:creator>Dal-Hee Min </dc:creator><dc:identifier>10.1039/b919971n</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b919971n</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-16</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b919971n</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b919298k&amp;RSS=1"><title>Direct template-free electrochemical growth of hexagonal CuSn tubes from an ionic liquid</title>
		<link>http://xlink.rsc.org/?DOI=b919298k&amp;RSS=1</link>
		<description>Free standing hexagonal hollow copper-tin tube arrays are formed by direct cathodic electrolysis in the 1-ethyl-3-methylimidazolium dicyanamide ionic liquid.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b919298k-ga.gif"/&gt;
	&lt;/p&gt;Yi-Ting Hsieh, Tin-Iao Leong, Chih-Chia Huang, Chen-Sheng Yeh, I-Wen Sun &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Yi-Ting Hsieh, Chem. Commun., 2010, DOI: 10.1039/b919298k&lt;br/&gt;
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		<dc:title>Direct template-free electrochemical growth of hexagonal CuSn tubes from an ionic liquid</dc:title>
		<dc:creator>Yi-Ting Hsieh</dc:creator>
		<dc:creator>Tin-Iao Leong </dc:creator><dc:creator>Chih-Chia Huang </dc:creator><dc:creator>Chen-Sheng Yeh </dc:creator><dc:creator>I-Wen Sun </dc:creator><dc:identifier>10.1039/b919298k</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b919298k</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-16</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b919298k</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b915843j&amp;RSS=1"><title>FLAG tagging by CuAAC and nanogram-scale purification of the target protein for a bioactive metabolite involved in circadian rhythmic leaf movement in Leguminosae</title>
		<link>http://xlink.rsc.org/?DOI=b915843j&amp;RSS=1</link>
		<description>A stepwise FLAG-tagging strategy for the purification of a target protein for bioactive metabolites is reported. A target protein of isolespedezate, a bioactive metabolite controlling plant nyctinasty, was identified by this method.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b915843j-ga.gif"/&gt;
	&lt;/p&gt;Yoshiyuki Manabe, Makoto Mukai, Satoko Ito, Nobuki Kato, Minoru Ueda &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Yoshiyuki Manabe, Chem. Commun., 2010, DOI: 10.1039/b915843j&lt;br/&gt;
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		<dc:title>FLAG tagging by CuAAC and nanogram-scale purification of the target protein for a bioactive metabolite involved in circadian rhythmic leaf movement in Leguminosae</dc:title>
		<dc:creator>Yoshiyuki Manabe</dc:creator>
		<dc:creator>Makoto Mukai </dc:creator><dc:creator>Satoko Ito </dc:creator><dc:creator>Nobuki Kato </dc:creator><dc:creator>Minoru Ueda </dc:creator><dc:identifier>10.1039/b915843j</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b915843j</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-16</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b915843j</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b917137a&amp;RSS=1"><title>A rapid and efficient strategy for preparation of super-hydrophobic surface with cross-linked cyclotriphosphazene/6F-bisphenol A copolymer microspheres</title>
		<link>http://xlink.rsc.org/?DOI=b917137a&amp;RSS=1</link>
		<description>A novel super-hydrophobic surface formed with cross-linked cyclotriphosphazene/6F-bisphenol A copolymer microspheres was prepared via a single-step precipitation polymerization and a technology-free dip-coating route.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b917137a-ga.gif"/&gt;
	&lt;/p&gt;Wei Wei, Xiaobin Huang, Xiaoli Zhao, Peng Zhang, Xiaozhen Tang &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Wei Wei, Chem. Commun., 2010, DOI: 10.1039/b917137a&lt;br/&gt;
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		<dc:title>A rapid and efficient strategy for preparation of super-hydrophobic surface with cross-linked cyclotriphosphazene/6F-bisphenol A copolymer microspheres</dc:title>
		<dc:creator>Wei Wei</dc:creator>
		<dc:creator>Xiaobin Huang </dc:creator><dc:creator>Xiaoli Zhao </dc:creator><dc:creator>Peng Zhang </dc:creator><dc:creator>Xiaozhen Tang </dc:creator><dc:identifier>10.1039/b917137a</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b917137a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-16</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b917137a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b918912b&amp;RSS=1"><title>A short, unsupported Cu(i)Cu(i) interaction, 2.65 A, in a dinuclear guanidine chloride complex</title>
		<link>http://xlink.rsc.org/?DOI=b918912b&amp;RSS=1</link>
		<description>The reaction of copper(i) chloride in THF with the guanidinate ligand Hhpp leads to the formation of a product with a short, unsupported Cu(i)-Cu(i) interaction of 2.65 A.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b918912b-ga.gif"/&gt;
	&lt;/p&gt;Gina M. Chiarella, Doris Y. Melgarejo, Alex Rozanski, Pierre Hempte, Lisa M. Perez, Christian Reber, John P. Fackler Jr. &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Gina M. Chiarella, Chem. Commun., 2010, DOI: 10.1039/b918912b&lt;br/&gt;
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		<dc:title>A short, unsupported Cu(i)Cu(i) interaction, 2.65 A, in a dinuclear guanidine chloride complex</dc:title>
		<dc:creator>Gina M. Chiarella</dc:creator>
		<dc:creator>Doris Y. Melgarejo </dc:creator><dc:creator>Alex Rozanski </dc:creator><dc:creator>Pierre Hempte </dc:creator><dc:creator>Lisa M. Perez </dc:creator><dc:creator>Christian Reber </dc:creator><dc:creator>John P. Fackler Jr. </dc:creator><dc:identifier>10.1039/b918912b</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b918912b</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-13</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b918912b</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b901889a&amp;RSS=1"><title>Selectivity in small molecule binding to human telomeric RNA and DNA quadruplexes</title>
		<link>http://xlink.rsc.org/?DOI=b901889a&amp;RSS=1</link>
		<description>Quadruplex RNAs are less well understood than their DNA counterparts, yet of potentially high biological relevance. The interactions of several quadruplex-binding ligands with telomeric RNA quadruplexes are reported and compared with their binding to the analogous DNA quadruplexes.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2009/b901889a-ga.gif"/&gt;
	&lt;/p&gt;Gavin Collie, Anthony P. Reszka, Shozeb M. Haider, Valerie Gabelica, Gary N. Parkinson, Stephen Neidle &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Gavin Collie, Chem. Commun., 2009, DOI: 10.1039/b901889a&lt;br/&gt;
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		<dc:title>Selectivity in small molecule binding to human telomeric RNA and DNA quadruplexes</dc:title>
		<dc:creator>Gavin Collie</dc:creator>
		<dc:creator>Anthony P. Reszka </dc:creator><dc:creator>Shozeb M. Haider </dc:creator><dc:creator>Valerie Gabelica </dc:creator><dc:creator>Gary N. Parkinson </dc:creator><dc:creator>Stephen Neidle </dc:creator><dc:identifier>10.1039/b901889a</dc:identifier>
		<dc:source>Chem. Commun., 2009, DOI: 10.1039/b901889a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-13</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b901889a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b915665h&amp;RSS=1"><title>Molecular tectonics: tubular crystals with controllable channel size and orientation</title>
		<link>http://xlink.rsc.org/?DOI=b915665h&amp;RSS=1</link>
		<description>Crystals offering controllable tubular channels with imposed size and orientation may be generated by combining a ZnSiF6 pillar as an infinite tecton and flexible bismonodentate organic tectons of different length.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b915665h-ga.gif"/&gt;
	&lt;/p&gt;Mei-Jin Lin, Abdelaziz Jouaiti, David Pocic, Nathalie Kyritsakas, Jean-Marc Planeix, Mir Wais Hosseini &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Mei-Jin Lin, Chem. Commun., 2010, DOI: 10.1039/b915665h&lt;br/&gt;
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		<dc:title>Molecular tectonics: tubular crystals with controllable channel size and orientation</dc:title>
		<dc:creator>Mei-Jin Lin</dc:creator>
		<dc:creator>Abdelaziz Jouaiti </dc:creator><dc:creator>David Pocic </dc:creator><dc:creator>Nathalie Kyritsakas </dc:creator><dc:creator>Jean-Marc Planeix </dc:creator><dc:creator>Mir Wais Hosseini </dc:creator><dc:identifier>10.1039/b915665h</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b915665h</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-13</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b915665h</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b919383a&amp;RSS=1"><title>Recycle of tin thiolate compounds relevant to ammonia-borane regeneration</title>
		<link>http://xlink.rsc.org/?DOI=b919383a&amp;RSS=1</link>
		<description>The use of benzenedithiol as a digestant for ammonia-borane spent fuel has been shown to result in tin thiolate compounds which we demonstrate can be recycled, yielding Bu3SnH and ortho-benzenedithiol for reintroduction to the ammonia-borane regeneration scheme.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b919383a-ga.gif"/&gt;
	&lt;/p&gt;Andrew D. Sutton, Benjamin L. Davis, Koyel X. Bhattacharyya, Bobby D. Ellis, John C. Gordon, Philip P. Power &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Andrew D. Sutton, Chem. Commun., 2010, DOI: 10.1039/b919383a&lt;br/&gt;
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		<dc:title>Recycle of tin thiolate compounds relevant to ammonia-borane regeneration</dc:title>
		<dc:creator>Andrew D. Sutton</dc:creator>
		<dc:creator>Benjamin L. Davis </dc:creator><dc:creator>Koyel X. Bhattacharyya </dc:creator><dc:creator>Bobby D. Ellis </dc:creator><dc:creator>John C. Gordon </dc:creator><dc:creator>Philip P. Power </dc:creator><dc:identifier>10.1039/b919383a</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b919383a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-13</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b919383a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b910575a&amp;RSS=1"><title>Unusual partner radical trimer formation in a host complex of cucurbit[8]uril, ruthenium(ii) tris-bipyridine linked phenol and methyl viologen</title>
		<link>http://xlink.rsc.org/?DOI=b910575a&amp;RSS=1</link>
		<description>A stable 1 : 1 : 1 inclusion complex of Ru(bpy)3-phenol (1), MV2+ and cucurbit[8]uril (CB[8]) is formed in aqueous solution. In the presence of triethanolamine (TEOA), a light-induced formation of the unusual partner radical trimer 1-(MV+[radical dot])2-CB[8] has been observed for the first time.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b910575a-ga.gif"/&gt;
	&lt;/p&gt;Shiguo Sun, Samir Andersson, Rong Zhang, Licheng Sun &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Shiguo Sun, Chem. Commun., 2010, DOI: 10.1039/b910575a&lt;br/&gt;
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		<dc:title>Unusual partner radical trimer formation in a host complex of cucurbit[8]uril, ruthenium(ii) tris-bipyridine linked phenol and methyl viologen</dc:title>
		<dc:creator>Shiguo Sun</dc:creator>
		<dc:creator>Samir Andersson </dc:creator><dc:creator>Rong Zhang </dc:creator><dc:creator>Licheng Sun </dc:creator><dc:identifier>10.1039/b910575a</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b910575a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-13</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b910575a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b917781g&amp;RSS=1"><title>CuO hollow nanostructures catalyze [3 + 2] cycloaddition of azides with terminal alkynes</title>
		<link>http://xlink.rsc.org/?DOI=b917781g&amp;RSS=1</link>
		<description>CuO hollow nanostructures have been used for the catalytic [3 + 2] cycloaddition of azides with terminal alkynes to provide the products in good yields with high regioselectivity.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b917781g-ga.gif"/&gt;
	&lt;/p&gt;Jee Young Kim, Ji Chan Park, Hyuntae Kang, Hyunjoon Song, Kang Hyun Park &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Jee Young Kim, Chem. Commun., 2010, DOI: 10.1039/b917781g&lt;br/&gt;
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		<dc:title>CuO hollow nanostructures catalyze [3 + 2] cycloaddition of azides with terminal alkynes</dc:title>
		<dc:creator>Jee Young Kim</dc:creator>
		<dc:creator>Ji Chan Park </dc:creator><dc:creator>Hyuntae Kang </dc:creator><dc:creator>Hyunjoon Song </dc:creator><dc:creator>Kang Hyun Park </dc:creator><dc:identifier>10.1039/b917781g</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b917781g</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-13</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b917781g</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b913209k&amp;RSS=1"><title>Energy barriers between H-bonded and stacked structures of 9-methyladenine1-methylthymine and 9-methylguanine1-methylcytosine complexes</title>
		<link>http://xlink.rsc.org/?DOI=b913209k&amp;RSS=1</link>
		<description>The energy barrier between stacked (S) and transition structures (TS) of methyladeninemethylthymine is high enough to support the existence of the stacked structure even at high temperatures.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b913209k-ga.gif"/&gt;
	&lt;/p&gt;Jiri Cerny, Pavel Hobza &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Jiri Cerny, Chem. Commun., 2010, DOI: 10.1039/b913209k&lt;br/&gt;
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		<dc:title>Energy barriers between H-bonded and stacked structures of 9-methyladenine1-methylthymine and 9-methylguanine1-methylcytosine complexes</dc:title>
		<dc:creator>Jiri Cerny</dc:creator>
		<dc:creator>Pavel Hobza </dc:creator><dc:identifier>10.1039/b913209k</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b913209k</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-13</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b913209k</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b917765e&amp;RSS=1"><title>Are there single-well hydrogen bonds in pyridine-dichloroacetic acid complexes?</title>
		<link>http://xlink.rsc.org/?DOI=b917765e&amp;RSS=1</link>
		<description>Isotope shifts of Cl2CHC18O2H-pyridine complexes in CD2Cl2 at low temperature reach a maximum when the basicities of the hydrogen-bond donors are matched, consistent with a mixture of tautomers.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b917765e-ga.gif"/&gt;
	&lt;/p&gt;Charles L. Perrin, Phaneendrasai Karri &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Charles L. Perrin, Chem. Commun., 2010, DOI: 10.1039/b917765e&lt;br/&gt;
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		<dc:title>Are there single-well hydrogen bonds in pyridine-dichloroacetic acid complexes?</dc:title>
		<dc:creator>Charles L. Perrin</dc:creator>
		<dc:creator>Phaneendrasai Karri </dc:creator><dc:identifier>10.1039/b917765e</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b917765e</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-13</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b917765e</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b916307g&amp;RSS=1"><title>13C Labeling reveals multiple amination reactions in the biosynthesis of a novel polyketide polyamine antibiotic zeamine from Dickeya zeae</title>
		<link>http://xlink.rsc.org/?DOI=b916307g&amp;RSS=1</link>
		<description>Zeamine, a novel polyamino-amide antibiotic, which has potent activity against methicillin-resistant Staphylococcus aureus (MRSA), may represent a novel extension of the mechanisms for incorporation of nitrogen into polyketide chains.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b916307g-ga.gif"/&gt;
	&lt;/p&gt;Jien Wu, Hai-Bao Zhang, Jin-Ling Xu, Russell J. Cox, Thomas J. Simpson, Lian-Hui Zhang &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Jien Wu, Chem. Commun., 2010, DOI: 10.1039/b916307g&lt;br/&gt;
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		<dc:title>13C Labeling reveals multiple amination reactions in the biosynthesis of a novel polyketide polyamine antibiotic zeamine from Dickeya zeae</dc:title>
		<dc:creator>Jien Wu</dc:creator>
		<dc:creator>Hai-Bao Zhang </dc:creator><dc:creator>Jin-Ling Xu </dc:creator><dc:creator>Russell J. Cox </dc:creator><dc:creator>Thomas J. Simpson </dc:creator><dc:creator>Lian-Hui Zhang </dc:creator><dc:identifier>10.1039/b916307g</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b916307g</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-13</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b916307g</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b918330b&amp;RSS=1"><title>Unique metabolites of Pestalotiopsis fici suggest a biosynthetic hypothesis involving a Diels-Alder reaction and then mechanistic diversification</title>
		<link>http://xlink.rsc.org/?DOI=b918330b&amp;RSS=1</link>
		<description>Chloropupukeanolides A (1) and B (2), unprecedented spiroketal peroxides, and chloropupukeanone A (3), three metabolites featuring a chlorinated pupukeanane core, were isolated from an endophytic fungus Pestalotiopsis fici, with 1 showing significant anti-HIV-1 and cytotoxic effects.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b918330b-ga.gif"/&gt;
	&lt;/p&gt;Ling Liu, Shubin Niu, Xinhua Lu, Xulin Chen, Hua Zhang, Liangdong Guo, Yongsheng Che &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Ling Liu, Chem. Commun., 2010, DOI: 10.1039/b918330b&lt;br/&gt;
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		<dc:title>Unique metabolites of Pestalotiopsis fici suggest a biosynthetic hypothesis involving a Diels-Alder reaction and then mechanistic diversification</dc:title>
		<dc:creator>Ling Liu</dc:creator>
		<dc:creator>Shubin Niu </dc:creator><dc:creator>Xinhua Lu </dc:creator><dc:creator>Xulin Chen </dc:creator><dc:creator>Hua Zhang </dc:creator><dc:creator>Liangdong Guo </dc:creator><dc:creator>Yongsheng Che </dc:creator><dc:identifier>10.1039/b918330b</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b918330b</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-13</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b918330b</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b918626c&amp;RSS=1"><title>Cyanative alkene-aldehyde coupling: Ni(0)-NHC-Et2AlCN mediated chromanol synthesis with high cis-selectivity at room temperature</title>
		<link>http://xlink.rsc.org/?DOI=b918626c&amp;RSS=1</link>
		<description>Several classes of Ni(0) mediated cyanative alkene-aldehyde coupling reactions are described.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b918626c-ga.gif"/&gt;
	&lt;/p&gt;Chun-Yu Ho &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Chun-Yu Ho, Chem. Commun., 2010, DOI: 10.1039/b918626c&lt;br/&gt;
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		<dc:title>Cyanative alkene-aldehyde coupling: Ni(0)-NHC-Et2AlCN mediated chromanol synthesis with high cis-selectivity at room temperature</dc:title>
		<dc:creator>Chun-Yu Ho</dc:creator>
		<dc:identifier>10.1039/b918626c</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b918626c</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-13</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b918626c</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b916426j&amp;RSS=1"><title>Porous ionic/molecular crystal composed of highly symmetric magnetic clusters</title>
		<link>http://xlink.rsc.org/?DOI=b916426j&amp;RSS=1</link>
		<description>A porous ionic/molecular crystal composed of discrete triakis tetrahedral Co8 clusters with an ideal Td symmetry shows not only spin glass, canted antiferromagnetism and guest modulated magnetic behaviors but also high CO2 adsorption ability and exceptional CO2/CH4 selectivity at ambient conditions.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b916426j-ga.gif"/&gt;
	&lt;/p&gt;Xiao-Ning Cheng, Wei Xue, Jian-Bin Lin, Xiao-Ming Chen &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Xiao-Ning Cheng, Chem. Commun., 2010, DOI: 10.1039/b916426j&lt;br/&gt;
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		<dc:title>Porous ionic/molecular crystal composed of highly symmetric magnetic clusters</dc:title>
		<dc:creator>Xiao-Ning Cheng</dc:creator>
		<dc:creator>Wei Xue </dc:creator><dc:creator>Jian-Bin Lin </dc:creator><dc:creator>Xiao-Ming Chen </dc:creator><dc:identifier>10.1039/b916426j</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b916426j</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-13</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b916426j</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b914563j&amp;RSS=1"><title>Dioxygen mediated hydroacylation of vinyl sulfonates and sulfones on water</title>
		<link>http://xlink.rsc.org/?DOI=b914563j&amp;RSS=1</link>
		<description>We report a mild, facile method for the preparation of 1,4-keto-sulfonates and sulfones on water.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b914563j-ga.gif"/&gt;
	&lt;/p&gt;Vijay Chudasama, Richard J. Fitzmaurice, Jenna M. Ahern, Stephen Caddick &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Vijay Chudasama, Chem. Commun., 2010, DOI: 10.1039/b914563j&lt;br/&gt;
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		<dc:title>Dioxygen mediated hydroacylation of vinyl sulfonates and sulfones on water</dc:title>
		<dc:creator>Vijay Chudasama</dc:creator>
		<dc:creator>Richard J. Fitzmaurice </dc:creator><dc:creator>Jenna M. Ahern </dc:creator><dc:creator>Stephen Caddick </dc:creator><dc:identifier>10.1039/b914563j</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b914563j</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-13</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b914563j</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b916858c&amp;RSS=1"><title>Discovery of a green DNA probe for live-cell imaging</title>
		<link>http://xlink.rsc.org/?DOI=b916858c&amp;RSS=1</link>
		<description>We discovered a green fluorescent probe, C61, which can selectively label DNA in living cells.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2009/b916858c-ga.gif"/&gt;
	&lt;/p&gt;Suihan Feng, Yun Kyung Kim, Siqiang Yang, Young-Tae Chang &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Suihan Feng, Chem. Commun., 2009, DOI: 10.1039/b916858c&lt;br/&gt;
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		<dc:title>Discovery of a green DNA probe for live-cell imaging</dc:title>
		<dc:creator>Suihan Feng</dc:creator>
		<dc:creator>Yun Kyung Kim </dc:creator><dc:creator>Siqiang Yang </dc:creator><dc:creator>Young-Tae Chang </dc:creator><dc:identifier>10.1039/b916858c</dc:identifier>
		<dc:source>Chem. Commun., 2009, DOI: 10.1039/b916858c</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-12</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b916858c</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b919587d&amp;RSS=1"><title>Temperature-induced solid-phase oriented rearrangement route to the fabrication of NaNbO3 nanowires</title>
		<link>http://xlink.rsc.org/?DOI=b919587d&amp;RSS=1</link>
		<description>We proposed here a temperature-induced solid-phase oriented rearrangement route to the fabrication of NaNbO3 nanowires by using sandia octahedral molecular sieves (SOMS) Na2Nb2O6[middle dot]H2O as a precursor. The SOMS precursor was prepared by using metallic Nb powder as a raw material through the hydrothermal approach.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2009/b919587d-ga.gif"/&gt;
	&lt;/p&gt;Lei Liu, Bo Li, Dinghua Yu, Yuming Cui, Xingfu Zhou, Weiping Ding &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Lei Liu, Chem. Commun., 2009, DOI: 10.1039/b919587d&lt;br/&gt;
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		<dc:title>Temperature-induced solid-phase oriented rearrangement route to the fabrication of NaNbO3 nanowires</dc:title>
		<dc:creator>Lei Liu</dc:creator>
		<dc:creator>Bo Li </dc:creator><dc:creator>Dinghua Yu </dc:creator><dc:creator>Yuming Cui </dc:creator><dc:creator>Xingfu Zhou </dc:creator><dc:creator>Weiping Ding </dc:creator><dc:identifier>10.1039/b919587d</dc:identifier>
		<dc:source>Chem. Commun., 2009, DOI: 10.1039/b919587d</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-12</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b919587d</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b915775a&amp;RSS=1"><title>Spontaneous and reversible self-assembly of a polypeptide fragment of insulin-like growth factor binding protein-2 into fluorescent nanotubular structures</title>
		<link>http://xlink.rsc.org/?DOI=b915775a&amp;RSS=1</link>
		<description>The C-terminal fragment of IGFBP-2 undergoes spontaneous, reversible self-assembly into soluble nanotubes exhibiting enhanced fluorescence via a novel mechanism involving inter-molecular disulfide bonds.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b915775a-ga.gif"/&gt;
	&lt;/p&gt;Monalisa Swain, R. Thirupathi, B. Krishnarjuna, Erin M. Eaton, Megan M. Kibbey, Steven A. Rosenzweig, Hanudatta S. Atreya &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Monalisa Swain, Chem. Commun., 2010, DOI: 10.1039/b915775a&lt;br/&gt;
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		<dc:title>Spontaneous and reversible self-assembly of a polypeptide fragment of insulin-like growth factor binding protein-2 into fluorescent nanotubular structures</dc:title>
		<dc:creator>Monalisa Swain</dc:creator>
		<dc:creator>R. Thirupathi </dc:creator><dc:creator>B. Krishnarjuna </dc:creator><dc:creator>Erin M. Eaton </dc:creator><dc:creator>Megan M. Kibbey </dc:creator><dc:creator>Steven A. Rosenzweig </dc:creator><dc:creator>Hanudatta S. Atreya </dc:creator><dc:identifier>10.1039/b915775a</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b915775a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-12</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b915775a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b917195a&amp;RSS=1"><title>Human serum albumin coated iron oxide nanoparticles for efficient cell labeling</title>
		<link>http://xlink.rsc.org/?DOI=b917195a&amp;RSS=1</link>
		<description>A novel dopamine-plus-HSA (human serum albumin) approach was developed to functionalize iron oxide nanoparticles (IONPs), yielding nanoconjugates that are highly efficient in labeling various types of cell lines.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2009/b917195a-ga.gif"/&gt;
	&lt;/p&gt;Jin Xie, Jinhua Wang, Gang Niu, Jing Huang, Kai Chen, Xingguo Li, Xiaoyuan Chen &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Jin Xie, Chem. Commun., 2009, DOI: 10.1039/b917195a&lt;br/&gt;
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		<dc:title>Human serum albumin coated iron oxide nanoparticles for efficient cell labeling</dc:title>
		<dc:creator>Jin Xie</dc:creator>
		<dc:creator>Jinhua Wang </dc:creator><dc:creator>Gang Niu </dc:creator><dc:creator>Jing Huang </dc:creator><dc:creator>Kai Chen </dc:creator><dc:creator>Xingguo Li </dc:creator><dc:creator>Xiaoyuan Chen </dc:creator><dc:identifier>10.1039/b917195a</dc:identifier>
		<dc:source>Chem. Commun., 2009, DOI: 10.1039/b917195a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-12</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b917195a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b914218e&amp;RSS=1"><title>Two distinct [small beta]-sheet fibrils from silk protein</title>
		<link>http://xlink.rsc.org/?DOI=b914218e&amp;RSS=1</link>
		<description>This study showed that Bombyx mori silk protein could be selectively induced to fold into fibrils dominated by either cross- or parallel-[small beta]-sheet structure, where the [small beta]-strands arrange perpendicular or parallel to the long fibril axis, incubated in ethanol-water quiescently or in water under shear.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2009/b914218e-ga.gif"/&gt;
	&lt;/p&gt;Zuguang Gong, Lei Huang, Yuhong Yang, Xin Chen, Zhengzhong Shao &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Zuguang Gong, Chem. Commun., 2009, DOI: 10.1039/b914218e&lt;br/&gt;
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		<dc:title>Two distinct [small beta]-sheet fibrils from silk protein</dc:title>
		<dc:creator>Zuguang Gong</dc:creator>
		<dc:creator>Lei Huang </dc:creator><dc:creator>Yuhong Yang </dc:creator><dc:creator>Xin Chen </dc:creator><dc:creator>Zhengzhong Shao </dc:creator><dc:identifier>10.1039/b914218e</dc:identifier>
		<dc:source>Chem. Commun., 2009, DOI: 10.1039/b914218e</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-12</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b914218e</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b917156h&amp;RSS=1"><title>Synthesis of transition metal isocyanide compounds from carbonyl complexes via reaction with Li[Me3SiNR]</title>
		<link>http://xlink.rsc.org/?DOI=b917156h&amp;RSS=1</link>
		<description>Li[Me3SiNR], obtained by treatment of RNH2 with Me3SiCl and BunLi, is a convenient reagent for converting a carbonyl compound to its isocyanide counterpart.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2009/b917156h-ga.gif"/&gt;
	&lt;/p&gt;Wesley Sattler, Gerard Parkin &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Wesley Sattler, Chem. Commun., 2009, DOI: 10.1039/b917156h&lt;br/&gt;
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		<dc:title>Synthesis of transition metal isocyanide compounds from carbonyl complexes via reaction with Li[Me3SiNR]</dc:title>
		<dc:creator>Wesley Sattler</dc:creator>
		<dc:creator>Gerard Parkin </dc:creator><dc:identifier>10.1039/b917156h</dc:identifier>
		<dc:source>Chem. Commun., 2009, DOI: 10.1039/b917156h</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-12</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b917156h</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b917431a&amp;RSS=1"><title>Self-assembled, cogged hexameric nanotubes formed from pyrogallol[4]arenes with a unique branched side chain</title>
		<link>http://xlink.rsc.org/?DOI=b917431a&amp;RSS=1</link>
		<description>Hexameric pyrogallol[4]arene nanotubes interlock when the side chains are 3-pentyl but not when the side chains are linear or differently branched.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2009/b917431a-ga.gif"/&gt;
	&lt;/p&gt;Oleg V. Kulikov, Megan M. Daschbach, Carl R. Yamnitz, Nigam Rath, George W. Gokel &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Oleg V. Kulikov, Chem. Commun., 2009, DOI: 10.1039/b917431a&lt;br/&gt;
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		<dc:title>Self-assembled, cogged hexameric nanotubes formed from pyrogallol[4]arenes with a unique branched side chain</dc:title>
		<dc:creator>Oleg V. Kulikov</dc:creator>
		<dc:creator>Megan M. Daschbach </dc:creator><dc:creator>Carl R. Yamnitz </dc:creator><dc:creator>Nigam Rath </dc:creator><dc:creator>George W. Gokel </dc:creator><dc:identifier>10.1039/b917431a</dc:identifier>
		<dc:source>Chem. Commun., 2009, DOI: 10.1039/b917431a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-12</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b917431a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b917757d&amp;RSS=1"><title>Application of d6 transition metal complexes in fluorescence cell imaging</title>
		<link>http://xlink.rsc.org/?DOI=b917757d&amp;RSS=1</link>
		<description>The emerging area of the application of Ir, Re and Ru polypyridyl and organometallic complexes as lumophores in fluorescent cell imaging is reviewed.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b917757d-ga.gif"/&gt;
	&lt;/p&gt;Vanesa Fernandez-Moreira, Flora L. Thorp-Greenwood, Michael P. Coogan &lt;br/&gt;
(Feature Article from Chem. Commun.)&lt;br/&gt;
Vanesa Fernandez-Moreira, Chem. Commun., 2010, DOI: 10.1039/b917757d&lt;br/&gt;
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		<dc:title>Application of d6 transition metal complexes in fluorescence cell imaging</dc:title>
		<dc:creator>Vanesa Fernandez-Moreira</dc:creator>
		<dc:creator>Flora L. Thorp-Greenwood </dc:creator><dc:creator>Michael P. Coogan </dc:creator><dc:identifier>10.1039/b917757d</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b917757d</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-12</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b917757d</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b917711f&amp;RSS=1"><title>Room temperature Stille cross-coupling reaction of unreactive aryl chlorides and heteroaryl chlorides</title>
		<link>http://xlink.rsc.org/?DOI=b917711f&amp;RSS=1</link>
		<description>We have developed the first catalyst that can achieve efficient Stille coupling reactions of aryl chlorides and heteroaryl chlorides with organostannanes at room temperature.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b917711f-ga.gif"/&gt;
	&lt;/p&gt;Dong-Hwan Lee, Abu Taher, Wha-Seung Ahn, Myung-Jong Jin &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Dong-Hwan Lee, Chem. Commun., 2010, DOI: 10.1039/b917711f&lt;br/&gt;
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		<dc:title>Room temperature Stille cross-coupling reaction of unreactive aryl chlorides and heteroaryl chlorides</dc:title>
		<dc:creator>Dong-Hwan Lee</dc:creator>
		<dc:creator>Abu Taher </dc:creator><dc:creator>Wha-Seung Ahn </dc:creator><dc:creator>Myung-Jong Jin </dc:creator><dc:identifier>10.1039/b917711f</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b917711f</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-12</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b917711f</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b914457a&amp;RSS=1"><title>Single crystal structure of copper hexadecafluorophthalocyanine (F16CuPc) ribbon</title>
		<link>http://xlink.rsc.org/?DOI=b914457a&amp;RSS=1</link>
		<description>The single crystal structure of a micrometre-scale copper hexadecafluoro-phthalocyanine (F16CuPc) ribbon synthesized by vaporization-condensation-recrystallization (VCR) process was resolved by using a synchrotron X-ray diffractometer.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b914457a-ga.gif"/&gt;
	&lt;/p&gt;Seok Min Yoon, Hyun Jae Song, In-Chul Hwang, Kwang S. Kim, Hee Cheul Choi &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Seok Min Yoon, Chem. Commun., 2010, DOI: 10.1039/b914457a&lt;br/&gt;
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		<dc:title>Single crystal structure of copper hexadecafluorophthalocyanine (F16CuPc) ribbon</dc:title>
		<dc:creator>Seok Min Yoon</dc:creator>
		<dc:creator>Hyun Jae Song </dc:creator><dc:creator>In-Chul Hwang </dc:creator><dc:creator>Kwang S. Kim </dc:creator><dc:creator>Hee Cheul Choi </dc:creator><dc:identifier>10.1039/b914457a</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b914457a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-12</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b914457a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b919759a&amp;RSS=1"><title>Peculiar nanocomposite hydrogel with controllable multiple thermosensitivity: double phase transition and ternary stable states</title>
		<link>http://xlink.rsc.org/?DOI=b919759a&amp;RSS=1</link>
		<description>A novel nanocomposite hydrogel with controllable multiple thermosensitivity has been synthesized by introducing poly(ethylene glycol) into clay/poly(N-isopropylacrylamide) nanocomposite hydrogel, which exhibits double thermosensitive phase transition spontaneously.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2009/b919759a-ga.gif"/&gt;
	&lt;/p&gt;Yang Liu, Xiaoli Liu, Yongtao Wu, Bin Sun, Meifang Zhu, Makoto Takafuji, Hirotaka Ihara &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Yang Liu, Chem. Commun., 2009, DOI: 10.1039/b919759a&lt;br/&gt;
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		<dc:title>Peculiar nanocomposite hydrogel with controllable multiple thermosensitivity: double phase transition and ternary stable states</dc:title>
		<dc:creator>Yang Liu</dc:creator>
		<dc:creator>Xiaoli Liu </dc:creator><dc:creator>Yongtao Wu </dc:creator><dc:creator>Bin Sun </dc:creator><dc:creator>Meifang Zhu </dc:creator><dc:creator>Makoto Takafuji </dc:creator><dc:creator>Hirotaka Ihara </dc:creator><dc:identifier>10.1039/b919759a</dc:identifier>
		<dc:source>Chem. Commun., 2009, DOI: 10.1039/b919759a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-12</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b919759a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b919976d&amp;RSS=1"><title>Highly ordered transparent mesoporous TiO2 thin films: an attractive matrix for efficient immobilization and spectroelectrochemical characterization of cytochrome c</title>
		<link>http://xlink.rsc.org/?DOI=b919976d&amp;RSS=1</link>
		<description>We demonstrate remarkably fast incorporation, high loading and rapid redox switch of cytochrome c within thin films of periodically ordered nanocrystalline TiO2 deposited on transparent electrodes.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2009/b919976d-ga.gif"/&gt;
	&lt;/p&gt;Christophe Renault, Veronique Balland, Eugenia Martinez-Ferrero, Lionel Nicole, Clement Sanchez, Benoit Limoges &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Christophe Renault, Chem. Commun., 2009, DOI: 10.1039/b919976d&lt;br/&gt;
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		<dc:title>Highly ordered transparent mesoporous TiO2 thin films: an attractive matrix for efficient immobilization and spectroelectrochemical characterization of cytochrome c</dc:title>
		<dc:creator>Christophe Renault</dc:creator>
		<dc:creator>Veronique Balland </dc:creator><dc:creator>Eugenia Martinez-Ferrero </dc:creator><dc:creator>Lionel Nicole </dc:creator><dc:creator>Clement Sanchez </dc:creator><dc:creator>Benoit Limoges </dc:creator><dc:identifier>10.1039/b919976d</dc:identifier>
		<dc:source>Chem. Commun., 2009, DOI: 10.1039/b919976d</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-12</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b919976d</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b913284h&amp;RSS=1"><title>Enormous enhancement in photocurrent generation using electrochemically fabricated gold nanostructures</title>
		<link>http://xlink.rsc.org/?DOI=b913284h&amp;RSS=1</link>
		<description>Self-assembled monolayers of porphyrin fabricated on the surface of electrochemically deposited gold nanostructure exhibit enormous enhancement of photocurrents due to porphyrin excitation especially in the near-infra red region, where the localized surface plasmon resonance was responsible.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2009/b913284h-ga.gif"/&gt;
	&lt;/p&gt;Tsuyoshi Akiyama, Kenta Aiba, Kazuko Hoashi, Meng Wang, Kosuke Sugawa, Sunao Yamada &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Tsuyoshi Akiyama, Chem. Commun., 2009, DOI: 10.1039/b913284h&lt;br/&gt;
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		<dc:title>Enormous enhancement in photocurrent generation using electrochemically fabricated gold nanostructures</dc:title>
		<dc:creator>Tsuyoshi Akiyama</dc:creator>
		<dc:creator>Kenta Aiba </dc:creator><dc:creator>Kazuko Hoashi </dc:creator><dc:creator>Meng Wang </dc:creator><dc:creator>Kosuke Sugawa </dc:creator><dc:creator>Sunao Yamada </dc:creator><dc:identifier>10.1039/b913284h</dc:identifier>
		<dc:source>Chem. Commun., 2009, DOI: 10.1039/b913284h</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-12</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b913284h</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b917038c&amp;RSS=1"><title>A hierarchical Fe/ZSM-5 zeolite with superior catalytic performance for benzene hydroxylation to phenol</title>
		<link>http://xlink.rsc.org/?DOI=b917038c&amp;RSS=1</link>
		<description>Hierarchical structuring of Fe/ZSM-5 zeolite substantially increases the catalyst lifetime for benzene hydroxylation to phenol with nitrous oxide; the turnover number after one day on stream is almost four times higher than for conventional Fe/ZSM-5.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2009/b917038c-ga.gif"/&gt;
	&lt;/p&gt;Hongchuan Xin, Arjan Koekkoek, Qihua Yang, Rutger van Santen, Can Li, Emiel J. M. Hensen &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Hongchuan Xin, Chem. Commun., 2009, DOI: 10.1039/b917038c&lt;br/&gt;
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		<dc:title>A hierarchical Fe/ZSM-5 zeolite with superior catalytic performance for benzene hydroxylation to phenol</dc:title>
		<dc:creator>Hongchuan Xin</dc:creator>
		<dc:creator>Arjan Koekkoek </dc:creator><dc:creator>Qihua Yang </dc:creator><dc:creator>Rutger van Santen </dc:creator><dc:creator>Can Li </dc:creator><dc:creator>Emiel J. M. Hensen </dc:creator><dc:identifier>10.1039/b917038c</dc:identifier>
		<dc:source>Chem. Commun., 2009, DOI: 10.1039/b917038c</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-11</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b917038c</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b914242h&amp;RSS=1"><title>Synthesis of super hard Ni-B/diamond composite coatings by wet processes</title>
		<link>http://xlink.rsc.org/?DOI=b914242h&amp;RSS=1</link>
		<description>Ni-B/diamond composite coatings were prepared using electrophoretic deposition and electroless deposition methods, leading to extremely high hardness which is comparable to hard coatings prepared by dry processes.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2009/b914242h-ga.gif"/&gt;
	&lt;/p&gt;Hitoshi Ogihara, Atsushi Hara, Kazuyuki Miyamoto, Nabeen K. Shrestha, Takeshi Kaneda, Shigenori Ito, Tetsuo Saji &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Hitoshi Ogihara, Chem. Commun., 2009, DOI: 10.1039/b914242h&lt;br/&gt;
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		<dc:title>Synthesis of super hard Ni-B/diamond composite coatings by wet processes</dc:title>
		<dc:creator>Hitoshi Ogihara</dc:creator>
		<dc:creator>Atsushi Hara </dc:creator><dc:creator>Kazuyuki Miyamoto </dc:creator><dc:creator>Nabeen K. Shrestha </dc:creator><dc:creator>Takeshi Kaneda </dc:creator><dc:creator>Shigenori Ito </dc:creator><dc:creator>Tetsuo Saji </dc:creator><dc:identifier>10.1039/b914242h</dc:identifier>
		<dc:source>Chem. Commun., 2009, DOI: 10.1039/b914242h</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-11</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b914242h</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b917758b&amp;RSS=1"><title>Anticancer platinum complexes as non-innocent compounds for catalysis in aqueous media</title>
		<link>http://xlink.rsc.org/?DOI=b917758b&amp;RSS=1</link>
		<description>An efficient cyclization of alkyne-acids to enol-lactones catalyzed by anticancer platinum(ii) and platinum(iv) compounds is described. These compounds are not only DNA-binding complexes, they can also catalyze reactions in solvents such as acetone, methanol, water or blood plasma.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2009/b917758b-ga.gif"/&gt;
	&lt;/p&gt;Jose Aleman, Virginia del Solar, Carmen Navarro-Ranninger &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Jose Aleman, Chem. Commun., 2009, DOI: 10.1039/b917758b&lt;br/&gt;
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		<dc:title>Anticancer platinum complexes as non-innocent compounds for catalysis in aqueous media</dc:title>
		<dc:creator>Jose Aleman</dc:creator>
		<dc:creator>Virginia del Solar </dc:creator><dc:creator>Carmen Navarro-Ranninger </dc:creator><dc:identifier>10.1039/b917758b</dc:identifier>
		<dc:source>Chem. Commun., 2009, DOI: 10.1039/b917758b</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-11</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b917758b</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b913307k&amp;RSS=1"><title>ssPNA templated assembly of oligo(p-phenylenevinylene)s</title>
		<link>http://xlink.rsc.org/?DOI=b913307k&amp;RSS=1</link>
		<description>A single-stranded oligothymine peptide nucleic acid (PNA) was used as a template for the assembly of a chiral oligo(p-phenylenevinylene) diaminotriazine derivative in organic media revealing size controlled nanostructures.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b913307k-ga.gif"/&gt;
	&lt;/p&gt;Pim G. A. Janssen, Nico Meeuwenoord, Gijs van der Marel, Sara Jabbari-Farouji, Paul van der Schoot, Mathieu Surin, Zeljko Tomovic, E. W. Meijer, Albertus P. H. J. Schenning &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Pim G. A. Janssen, Chem. Commun., 2010, DOI: 10.1039/b913307k&lt;br/&gt;
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		<dc:title>ssPNA templated assembly of oligo(p-phenylenevinylene)s</dc:title>
		<dc:creator>Pim G. A. Janssen</dc:creator>
		<dc:creator>Nico Meeuwenoord </dc:creator><dc:creator>Gijs van der Marel </dc:creator><dc:creator>Sara Jabbari-Farouji </dc:creator><dc:creator>Paul van der Schoot </dc:creator><dc:creator>Mathieu Surin </dc:creator><dc:creator>Zeljko Tomovic </dc:creator><dc:creator>E. W. Meijer </dc:creator><dc:creator>Albertus P. H. J. Schenning </dc:creator><dc:identifier>10.1039/b913307k</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b913307k</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-11</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b913307k</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b914279g&amp;RSS=1"><title>Laser printing mediated cell patterning</title>
		<link>http://xlink.rsc.org/?DOI=b914279g&amp;RSS=1</link>
		<description>An approach for complex cell patterning, using laser printing, is described allowing essentially any cellular image or pattern to be rapidly fabricated.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2009/b914279g-ga.gif"/&gt;
	&lt;/p&gt;Albert Liberski, Rong Zhang, Mark Bradley &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Albert Liberski, Chem. Commun., 2009, DOI: 10.1039/b914279g&lt;br/&gt;
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		<dc:title>Laser printing mediated cell patterning</dc:title>
		<dc:creator>Albert Liberski</dc:creator>
		<dc:creator>Rong Zhang </dc:creator><dc:creator>Mark Bradley </dc:creator><dc:identifier>10.1039/b914279g</dc:identifier>
		<dc:source>Chem. Commun., 2009, DOI: 10.1039/b914279g</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-11</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b914279g</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b914761f&amp;RSS=1"><title>Targeted synthesis of a 3D porous aromatic framework for selective sorption of benzene</title>
		<link>http://xlink.rsc.org/?DOI=b914761f&amp;RSS=1</link>
		<description>A novel 3D porous aromatic framework (PAF) based on a tetraphenylmethane block and a triangular triazine ring been designed and synthesized, with 1109 m2 g-1 Langmuir surface area, and shows selective sorption of benzene.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2009/b914761f-ga.gif"/&gt;
	&lt;/p&gt;Hao Ren, Teng Ben, Ensi Wang, Xiaofei Jing, Ming Xue, Bingbing Liu, Yan Cui, Shilun Qiu, Guangshan Zhu &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Hao Ren, Chem. Commun., 2009, DOI: 10.1039/b914761f&lt;br/&gt;
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		<dc:title>Targeted synthesis of a 3D porous aromatic framework for selective sorption of benzene</dc:title>
		<dc:creator>Hao Ren</dc:creator>
		<dc:creator>Teng Ben </dc:creator><dc:creator>Ensi Wang </dc:creator><dc:creator>Xiaofei Jing </dc:creator><dc:creator>Ming Xue </dc:creator><dc:creator>Bingbing Liu </dc:creator><dc:creator>Yan Cui </dc:creator><dc:creator>Shilun Qiu </dc:creator><dc:creator>Guangshan Zhu </dc:creator><dc:identifier>10.1039/b914761f</dc:identifier>
		<dc:source>Chem. Commun., 2009, DOI: 10.1039/b914761f</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-11</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b914761f</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b913920f&amp;RSS=1"><title>Direct fabrication of mesoporous zeolite with a hollow capsular structure</title>
		<link>http://xlink.rsc.org/?DOI=b913920f&amp;RSS=1</link>
		<description>The coexistence of hollow structure and intracrystal mesopores is shown. Each particle is permeated by mesopore structures of the same size (3 nm). Higher resolution imaging reveals the zeolite crystal lattice.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2009/b913920f-ga.gif"/&gt;
	&lt;/p&gt;Jinjin Zhao, Zile Hua, Zhicheng Liu, Yongsheng Li, Limin Guo, Wenbo Bu, Xiangzhi Cui, Meiling Ruan, Hangrong Chen, Jianlin Shi &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Jinjin Zhao, Chem. Commun., 2009, DOI: 10.1039/b913920f&lt;br/&gt;
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		<dc:title>Direct fabrication of mesoporous zeolite with a hollow capsular structure</dc:title>
		<dc:creator>Jinjin Zhao</dc:creator>
		<dc:creator>Zile Hua </dc:creator><dc:creator>Zhicheng Liu </dc:creator><dc:creator>Yongsheng Li </dc:creator><dc:creator>Limin Guo </dc:creator><dc:creator>Wenbo Bu </dc:creator><dc:creator>Xiangzhi Cui </dc:creator><dc:creator>Meiling Ruan </dc:creator><dc:creator>Hangrong Chen </dc:creator><dc:creator>Jianlin Shi </dc:creator><dc:identifier>10.1039/b913920f</dc:identifier>
		<dc:source>Chem. Commun., 2009, DOI: 10.1039/b913920f</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-10</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b913920f</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b919364b&amp;RSS=1"><title>An enzymatic route to 5-deoxy-5-[18F]fluoro-d-ribose, a [18F]-fluorinated sugar for PET imaging</title>
		<link>http://xlink.rsc.org/?DOI=b919364b&amp;RSS=1</link>
		<description>An efficient two-step biotransformation utilising the fluorinase enzyme has been developed for the synthesis of [18F]-5-fluoro-5-deoxyribose.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2010/b919364b-ga.gif"/&gt;
	&lt;/p&gt;Mayca Onega, Juozas Domarkas, Hai Deng, Lutz F. Schweiger, Timothy A. D. Smith, Andrew E. Welch, Christophe Plisson, Antony D. Gee, David O'Hagan &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Mayca Onega, Chem. Commun., 2010, DOI: 10.1039/b919364b&lt;br/&gt;
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		<dc:title>An enzymatic route to 5-deoxy-5-[18F]fluoro-d-ribose, a [18F]-fluorinated sugar for PET imaging</dc:title>
		<dc:creator>Mayca Onega</dc:creator>
		<dc:creator>Juozas Domarkas </dc:creator><dc:creator>Hai Deng </dc:creator><dc:creator>Lutz F. Schweiger </dc:creator><dc:creator>Timothy A. D. Smith </dc:creator><dc:creator>Andrew E. Welch </dc:creator><dc:creator>Christophe Plisson </dc:creator><dc:creator>Antony D. Gee </dc:creator><dc:creator>David O'Hagan </dc:creator><dc:identifier>10.1039/b919364b</dc:identifier>
		<dc:source>Chem. Commun., 2010, DOI: 10.1039/b919364b</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-10</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b919364b</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b916092b&amp;RSS=1"><title>Transformation of framework solids into processable metallo-polymers</title>
		<link>http://xlink.rsc.org/?DOI=b916092b&amp;RSS=1</link>
		<description>A novel design strategy that extends the metal-organic frameworks into tractable metallo-polymers was explored by incorporating a series of alkyl side chains to an organic linker, in which drastic solid to solid transformation is observed.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2009/b916092b-ga.gif"/&gt;
	&lt;/p&gt;Eun-Young Choi, Chunji Gao, Hong-Jun Lee, O-Pil Kwon, Suck-Hyun Lee &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Eun-Young Choi, Chem. Commun., 2009, DOI: 10.1039/b916092b&lt;br/&gt;
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&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry</content:encoded>
		<dc:title>Transformation of framework solids into processable metallo-polymers</dc:title>
		<dc:creator>Eun-Young Choi</dc:creator>
		<dc:creator>Chunji Gao </dc:creator><dc:creator>Hong-Jun Lee </dc:creator><dc:creator>O-Pil Kwon </dc:creator><dc:creator>Suck-Hyun Lee </dc:creator><dc:identifier>10.1039/b916092b</dc:identifier>
		<dc:source>Chem. Commun., 2009, DOI: 10.1039/b916092b</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-10</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b916092b</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b916940g&amp;RSS=1"><title>Ceria-terbia solid solution nanobelts with high catalytic activities for CO oxidation</title>
		<link>http://xlink.rsc.org/?DOI=b916940g&amp;RSS=1</link>
		<description>Ceria-terbia solid solution nanobelts were prepared by an electrochemical route and tested as catalysts of high activity for CO oxidation.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2009/b916940g-ga.gif"/&gt;
	&lt;/p&gt;Gao-Ren Li, Dun-Lin Qu, Zi-Long Wang, Cheng-Yong Su, Ye-Xiang Tong, Laurent Arurault &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Gao-Ren Li, Chem. Commun., 2009, DOI: 10.1039/b916940g&lt;br/&gt;
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&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry</content:encoded>
		<dc:title>Ceria-terbia solid solution nanobelts with high catalytic activities for CO oxidation</dc:title>
		<dc:creator>Gao-Ren Li</dc:creator>
		<dc:creator>Dun-Lin Qu </dc:creator><dc:creator>Zi-Long Wang </dc:creator><dc:creator>Cheng-Yong Su </dc:creator><dc:creator>Ye-Xiang Tong </dc:creator><dc:creator>Laurent Arurault </dc:creator><dc:identifier>10.1039/b916940g</dc:identifier>
		<dc:source>Chem. Commun., 2009, DOI: 10.1039/b916940g</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-10</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b916940g</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b912472a&amp;RSS=1"><title>Anisotropic ionic conductivities in lyotropic supramolecular liquid crystals</title>
		<link>http://xlink.rsc.org/?DOI=b912472a&amp;RSS=1</link>
		<description>The designed aromatic amide discotic molecule with sulfonic acid groups at its periphery exhibits a hexagonal supramolecular columnar liquid crystalline phase, which leads to the achievement of anisotropic ionic conductivity through macroscopically aligning the ionic channels.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/CC/2009/b912472a-ga.gif"/&gt;
	&lt;/p&gt;Youju Huang, Yuanhua Cong, Junjun Li, Daoliang Wang, Jingtuo Zhang, Lu Xu, Weili Li, Liangbin Li, Guoqiang Pan, Chuanlu Yang &lt;br/&gt;
(Communication from Chem. Commun.)&lt;br/&gt;
Youju Huang, Chem. Commun., 2009, DOI: 10.1039/b912472a&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</content:encoded>
		<dc:title>Anisotropic ionic conductivities in lyotropic supramolecular liquid crystals</dc:title>
		<dc:creator>Youju Huang</dc:creator>
		<dc:creator>Yuanhua Cong </dc:creator><dc:creator>Junjun Li </dc:creator><dc:creator>Daoliang Wang </dc:creator><dc:creator>Jingtuo Zhang </dc:creator><dc:creator>Lu Xu </dc:creator><dc:creator>Weili Li </dc:creator><dc:creator>Liangbin Li </dc:creator><dc:creator>Guoqiang Pan </dc:creator><dc:creator>Chuanlu Yang </dc:creator><dc:identifier>10.1039/b912472a</dc:identifier>
		<dc:source>Chem. Commun., 2009, DOI: 10.1039/b912472a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-10</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b912472a</dc:identifier>
	</item>
</rdf:RDF>
