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		<description>RSC - New J. Chem. latest articles</description>
		<link>http://xlink.rsc.org/jumptojournal.cfm?journal_code=NJ</link>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
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		<prism:issn>1144-0546</prism:issn><prism:eIssn>1369-9261</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 - New J. Chem. latest articles</dc:description>
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	<item rdf:about="http://xlink.rsc.org/?DOI=b9nj00453j&amp;RSS=1"><title>Enhanced photoluminescence and the self-assembled fibrillar nanostructure of 5-(cholesteryloxy)methyl-8-hydroxyquinoline lithium in a gel state</title>
		<link>http://xlink.rsc.org/?DOI=b9nj00453j&amp;RSS=1</link>
		<description>A soluble, highly efficient, fluorescent, organometallic gelator, LiChQ, was synthesized through the modification of LiQ with cholesterol.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00453j-ga.gif"/&gt;
	&lt;/p&gt;Sheng Kong, Lixin Xiao, Zhijian Chen, Xingzhong Yan, Bo Qu, Shufeng Wang, Qihuang Gong &lt;br/&gt;
(Paper from New J. Chem.)&lt;br/&gt;
Sheng Kong, New J. Chem., 2010, DOI: 10.1039/b9nj00453j&lt;br/&gt;
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		<dc:title>Enhanced photoluminescence and the self-assembled fibrillar nanostructure of 5-(cholesteryloxy)methyl-8-hydroxyquinoline lithium in a gel state</dc:title>
		<dc:creator>Sheng Kong</dc:creator>
		<dc:creator>Lixin Xiao </dc:creator><dc:creator>Zhijian Chen </dc:creator><dc:creator>Xingzhong Yan </dc:creator><dc:creator>Bo Qu </dc:creator><dc:creator>Shufeng Wang </dc:creator><dc:creator>Qihuang Gong </dc:creator><dc:identifier>10.1039/b9nj00453j</dc:identifier>
		<dc:source>New J. Chem., 2010, DOI: 10.1039/b9nj00453j</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-12-09</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/b9nj00453j</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9nj00420c&amp;RSS=1"><title>One-pot synthesis of new thio-derivatives of C60 with the unexpected formation of a thiazolidine-fulleropyrrolidine</title>
		<link>http://xlink.rsc.org/?DOI=b9nj00420c&amp;RSS=1</link>
		<description>One-pot Prato reactions of C60 with amino acids and aldehydes afford five new fullerene derivatives via 1,3-dipolar cycloaddition. These include the thiazolidine-fulleropyrrolidine 3, the formation of which relies on the presence of the active S-H hydrogen in 1.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00420c-ga.gif"/&gt;
	&lt;/p&gt;Chuanbao Chen, Xiaofang Li, Shangfeng Yang &lt;br/&gt;
(Paper from New J. Chem.)&lt;br/&gt;
Chuanbao Chen, New J. Chem., 2010, DOI: 10.1039/b9nj00420c&lt;br/&gt;
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		<dc:title>One-pot synthesis of new thio-derivatives of C60 with the unexpected formation of a thiazolidine-fulleropyrrolidine</dc:title>
		<dc:creator>Chuanbao Chen</dc:creator>
		<dc:creator>Xiaofang Li </dc:creator><dc:creator>Shangfeng Yang </dc:creator><dc:identifier>10.1039/b9nj00420c</dc:identifier>
		<dc:source>New J. Chem., 2010, DOI: 10.1039/b9nj00420c</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-12-09</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/b9nj00420c</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9nj00405j&amp;RSS=1"><title>Efficient electrolyte of N,N[prime or minute]-bis(salicylidene)ethylenediamine zinc(ii) iodide in dye-sensitized solar cells</title>
		<link>http://xlink.rsc.org/?DOI=b9nj00405j&amp;RSS=1</link>
		<description>N,N[prime or minute]-Bis(salicylidene)ethylenediamine zinc(ii) iodide (ZnLI2) was synthesized and applied as an efficient electrolyte in dye-sensitized solar cells, and found to have a photoelectric conversion efficiency of 7.75% with electrolyte E2 under 100 mW cm-2 irradiation.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00405j-ga.gif"/&gt;
	&lt;/p&gt;Shuming Yang, Huizhi Kou, Hongjun Wang, Ke Cheng, Jichao Wang &lt;br/&gt;
(Paper from New J. Chem.)&lt;br/&gt;
Shuming Yang, New J. Chem., 2010, DOI: 10.1039/b9nj00405j&lt;br/&gt;
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		<dc:title>Efficient electrolyte of N,N[prime or minute]-bis(salicylidene)ethylenediamine zinc(ii) iodide in dye-sensitized solar cells</dc:title>
		<dc:creator>Shuming Yang</dc:creator>
		<dc:creator>Huizhi Kou </dc:creator><dc:creator>Hongjun Wang </dc:creator><dc:creator>Ke Cheng </dc:creator><dc:creator>Jichao Wang </dc:creator><dc:identifier>10.1039/b9nj00405j</dc:identifier>
		<dc:source>New J. Chem., 2010, DOI: 10.1039/b9nj00405j</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-12-08</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/b9nj00405j</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9nj00520j&amp;RSS=1"><title>Conjugated ethynylene-fluorene polymers with electro-donating TTF as pendant groups: Synthesis, electrochemical and spectroscopic properties</title>
		<link>http://xlink.rsc.org/?DOI=b9nj00520j&amp;RSS=1</link>
		<description>A series of conjugated ethynylene-fluorene polymers with TTF as pendant groups were synthesized. These polymers exhibited good solubility and improving conductivity up to about 1-3 [times] 10-3 S cm-1.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00520j-ga.gif"/&gt;
	&lt;/p&gt;Xuechao Zhang, Chengyun Wang, Guoqiao Lai, Lei Zhang, Yongjia Shen &lt;br/&gt;
(Paper from New J. Chem.)&lt;br/&gt;
Xuechao Zhang, New J. Chem., 2010, DOI: 10.1039/b9nj00520j&lt;br/&gt;
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		<dc:title>Conjugated ethynylene-fluorene polymers with electro-donating TTF as pendant groups: Synthesis, electrochemical and spectroscopic properties</dc:title>
		<dc:creator>Xuechao Zhang</dc:creator>
		<dc:creator>Chengyun Wang </dc:creator><dc:creator>Guoqiao Lai </dc:creator><dc:creator>Lei Zhang </dc:creator><dc:creator>Yongjia Shen </dc:creator><dc:identifier>10.1039/b9nj00520j</dc:identifier>
		<dc:source>New J. Chem., 2010, DOI: 10.1039/b9nj00520j</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-12-08</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/b9nj00520j</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9nj00411d&amp;RSS=1"><title>Investigation of sublimation with and without dissociation in the chloride and nitrate salts of 4-(1-hydroxy-1,2-diphenylethyl)pyridine</title>
		<link>http://xlink.rsc.org/?DOI=b9nj00411d&amp;RSS=1</link>
		<description>Both 1H+[middle dot]Cl- and 1H+[middle dot]NO3- sublime and recrystallize on heating, the former with dissociation and loss of HCl. The two salts are isostructural, but Hirschfeld surface analysis shows significant differences between the intermolecular interactions.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00411d-ga.gif"/&gt;
	&lt;/p&gt;Nikoletta B. Bathori, Petra Bombicz, Susan A. Bourne, Gerhard A. Venter &lt;br/&gt;
(Paper from New J. Chem.)&lt;br/&gt;
Nikoletta B. Bathori, New J. Chem., 2010, DOI: 10.1039/b9nj00411d&lt;br/&gt;
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		<dc:title>Investigation of sublimation with and without dissociation in the chloride and nitrate salts of 4-(1-hydroxy-1,2-diphenylethyl)pyridine</dc:title>
		<dc:creator>Nikoletta B. Bathori</dc:creator>
		<dc:creator>Petra Bombicz </dc:creator><dc:creator>Susan A. Bourne </dc:creator><dc:creator>Gerhard A. Venter </dc:creator><dc:identifier>10.1039/b9nj00411d</dc:identifier>
		<dc:source>New J. Chem., 2010, DOI: 10.1039/b9nj00411d</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-12-07</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/b9nj00411d</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b923796h&amp;RSS=1"><title>New year, new resolutions, new impact for NJC...</title>
		<link>http://xlink.rsc.org/?DOI=b923796h&amp;RSS=1</link>
		<description>For its 34th year of publication, the editors of NJC are looking forward to the continuing upward progression of the Journal, with the support of its board, referees and authors.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/NJ/2010/b923796h-ga.gif"/&gt;
	&lt;/p&gt;
(Editorial from New J. Chem.)&lt;br/&gt;
New J. Chem., 2010, DOI: 10.1039/b923796h&lt;br/&gt;
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		<dc:title>New year, new resolutions, new impact for NJC...</dc:title>
		<dc:creator>RSC</dc:creator>
		<dc:identifier>10.1039/b923796h</dc:identifier>
		<dc:source>New J. Chem., 2010, DOI: 10.1039/b923796h</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-12-04</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/b923796h</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9nj00469f&amp;RSS=1"><title>Grafting of monoglyceride molecules for the design of hydrophilic and stable porous silicon surfaces</title>
		<link>http://xlink.rsc.org/?DOI=b9nj00469f&amp;RSS=1</link>
		<description>Hydrophilic chemically stable porous silicon surfaces are generated by surface functionalisation with polar head terminated lipid biomolecules of the monoglyceride type. Two approaches to anchor the monoglyceride moiety to porous silicon surfaces are presented.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00469f-ga.gif"/&gt;
	&lt;/p&gt;Stephanie Pace, Philippe Gonzalez, Jean-Marie Devoisselle, Pierre-Emmanuel Milhiet, Daniel Brunel, Frederique Cunin &lt;br/&gt;
(Letter from New J. Chem.)&lt;br/&gt;
Stephanie Pace, New J. Chem., 2010, DOI: 10.1039/b9nj00469f&lt;br/&gt;
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		<dc:title>Grafting of monoglyceride molecules for the design of hydrophilic and stable porous silicon surfaces</dc:title>
		<dc:creator>Stephanie Pace</dc:creator>
		<dc:creator>Philippe Gonzalez </dc:creator><dc:creator>Jean-Marie Devoisselle </dc:creator><dc:creator>Pierre-Emmanuel Milhiet </dc:creator><dc:creator>Daniel Brunel </dc:creator><dc:creator>Frederique Cunin </dc:creator><dc:identifier>10.1039/b9nj00469f</dc:identifier>
		<dc:source>New J. Chem., 2010, DOI: 10.1039/b9nj00469f</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-12-03</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/b9nj00469f</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9nj00515c&amp;RSS=1"><title>Modulating the luminescence of an iridium(iii) complex incorporating a di(2-picolyl)anilino-appended bipyridine ligand with Zn2+ cations</title>
		<link>http://xlink.rsc.org/?DOI=b9nj00515c&amp;RSS=1</link>
		<description>The presence of Zn2+ ions specifically perturbs the excited state of an Ir(iii) complex, giving rise to a blue-shifted absorption and emission, and a shorter luminescence lifetime.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00515c-ga.gif"/&gt;
	&lt;/p&gt;Juan C. Araya, Juana Gajardo, Sergio A. Moya, Pedro Aguirre, Loic Toupet, J. A. Gareth Williams, Muriel Escadeillas, Hubert Le Bozec, Veronique Guerchais &lt;br/&gt;
(Letter from New J. Chem.)&lt;br/&gt;
Juan C. Araya, New J. Chem., 2010, DOI: 10.1039/b9nj00515c&lt;br/&gt;
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		<dc:title>Modulating the luminescence of an iridium(iii) complex incorporating a di(2-picolyl)anilino-appended bipyridine ligand with Zn2+ cations</dc:title>
		<dc:creator>Juan C. Araya</dc:creator>
		<dc:creator>Juana Gajardo </dc:creator><dc:creator>Sergio A. Moya </dc:creator><dc:creator>Pedro Aguirre </dc:creator><dc:creator>Loic Toupet </dc:creator><dc:creator>J. A. Gareth Williams </dc:creator><dc:creator>Muriel Escadeillas </dc:creator><dc:creator>Hubert Le Bozec </dc:creator><dc:creator>Veronique Guerchais </dc:creator><dc:identifier>10.1039/b9nj00515c</dc:identifier>
		<dc:source>New J. Chem., 2010, DOI: 10.1039/b9nj00515c</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-12-01</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/b9nj00515c</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9nj00218a&amp;RSS=1"><title>A cucurbit[8]uril inclusion complex with 1,7-dimethyl-1,4,7,10-tetraazacyclododecane tetrachloride</title>
		<link>http://xlink.rsc.org/?DOI=b9nj00218a&amp;RSS=1</link>
		<description>The inclusion complex of DMC@CB[8] shows a sexfoil packing structure compared to the aligned structure in the free cucurbit[8]uril.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00218a-ga.gif"/&gt;
	&lt;/p&gt;Wu Xiao-jun, Hu Kai, Meng Xiang-gao, Cheng Gong-zhen &lt;br/&gt;
(Letter from New J. Chem.)&lt;br/&gt;
Wu Xiao-jun, New J. Chem., 2010, DOI: 10.1039/b9nj00218a&lt;br/&gt;
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		<dc:title>A cucurbit[8]uril inclusion complex with 1,7-dimethyl-1,4,7,10-tetraazacyclododecane tetrachloride</dc:title>
		<dc:creator>Wu Xiao-jun</dc:creator>
		<dc:creator>Hu Kai </dc:creator><dc:creator>Meng Xiang-gao </dc:creator><dc:creator>Cheng Gong-zhen </dc:creator><dc:identifier>10.1039/b9nj00218a</dc:identifier>
		<dc:source>New J. Chem., 2010, DOI: 10.1039/b9nj00218a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-27</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/b9nj00218a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9nj00588a&amp;RSS=1"><title>Mechanically induced reactions in organic solids: liquid eutectics or solid-state processes?</title>
		<link>http://xlink.rsc.org/?DOI=b9nj00588a&amp;RSS=1</link>
		<description>A thorough investigation of the solvent-free reaction between solid o-vanillin and p-toluidine has shown that mechanochemical transformations, which appear to be solid-state processes, may in fact occur in a liquid phase.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00588a-ga.gif"/&gt;
	&lt;/p&gt;Oleksandr Dolotko, Jerzy W. Wiench, Kevin W. Dennis, Vitalij K. Pecharsky, Viktor P. Balema &lt;br/&gt;
(Letter from New J. Chem.)&lt;br/&gt;
Oleksandr Dolotko, New J. Chem., 2010, DOI: 10.1039/b9nj00588a&lt;br/&gt;
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		<dc:title>Mechanically induced reactions in organic solids: liquid eutectics or solid-state processes?</dc:title>
		<dc:creator>Oleksandr Dolotko</dc:creator>
		<dc:creator>Jerzy W. Wiench </dc:creator><dc:creator>Kevin W. Dennis </dc:creator><dc:creator>Vitalij K. Pecharsky </dc:creator><dc:creator>Viktor P. Balema </dc:creator><dc:identifier>10.1039/b9nj00588a</dc:identifier>
		<dc:source>New J. Chem., 2010, DOI: 10.1039/b9nj00588a</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/b9nj00588a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9nj00355j&amp;RSS=1"><title>Crystal structures and sodium/silver distributions within the ionic conductors Na5Ag2Fe3(As2O7)4 and Na2Ag5Fe3(P2O7)4</title>
		<link>http://xlink.rsc.org/?DOI=b9nj00355j&amp;RSS=1</link>
		<description>Crystal structures of new Na5Ag2Fe3(As2O7)4 and Na2Ag5Fe3(P2O7)4 compounds are reported.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00355j-ga.gif"/&gt;
	&lt;/p&gt;Eric Quarez, Olivier Mentre, Karim Djellab, Christian Masquelier &lt;br/&gt;
(Paper from New J. Chem.)&lt;br/&gt;
Eric Quarez, New J. Chem., 2010, DOI: 10.1039/b9nj00355j&lt;br/&gt;
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		<dc:title>Crystal structures and sodium/silver distributions within the ionic conductors Na5Ag2Fe3(As2O7)4 and Na2Ag5Fe3(P2O7)4</dc:title>
		<dc:creator>Eric Quarez</dc:creator>
		<dc:creator>Olivier Mentre </dc:creator><dc:creator>Karim Djellab </dc:creator><dc:creator>Christian Masquelier </dc:creator><dc:identifier>10.1039/b9nj00355j</dc:identifier>
		<dc:source>New J. Chem., 2010, DOI: 10.1039/b9nj00355j</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/b9nj00355j</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9nj00277d&amp;RSS=1"><title>Cytotoxic and genotoxic assessment of glycolipid-reduced and -capped gold and silver nanoparticles</title>
		<link>http://xlink.rsc.org/?DOI=b9nj00277d&amp;RSS=1</link>
		<description>No cytotoxicity and genotoxicity: sophorolipid (a class of glycolipid)-conjugated silver and gold nanoparticles do not show any cytotoxic and genotoxic effects up to 100 [small mu]M metal concentrations.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00277d-ga.gif"/&gt;
	&lt;/p&gt;Sanjay Singh, V. D'Britto, A. A. Prabhune, C. V. Ramana, Alok Dhawan, B. L. V. Prasad &lt;br/&gt;
(Paper from New J. Chem.)&lt;br/&gt;
Sanjay Singh, New J. Chem., 2010, DOI: 10.1039/b9nj00277d&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>Cytotoxic and genotoxic assessment of glycolipid-reduced and -capped gold and silver nanoparticles</dc:title>
		<dc:creator>Sanjay Singh</dc:creator>
		<dc:creator>V. D'Britto </dc:creator><dc:creator>A. A. Prabhune </dc:creator><dc:creator>C. V. Ramana </dc:creator><dc:creator>Alok Dhawan </dc:creator><dc:creator>B. L. V. Prasad </dc:creator><dc:identifier>10.1039/b9nj00277d</dc:identifier>
		<dc:source>New J. Chem., 2010, DOI: 10.1039/b9nj00277d</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/b9nj00277d</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9nj00200f&amp;RSS=1"><title>Apolar ortho-phenylene ethynylene oligomers: conformational ordering without intermolecular aggregation</title>
		<link>http://xlink.rsc.org/?DOI=b9nj00200f&amp;RSS=1</link>
		<description>Non-polar alkoxy substituted ortho-phenylene ethynylene (o-PE) oligomers with lengths up to nine units have been shown to adopt helical conformations in heptane by NMR and CD spectroscopy, while chloroform promotes extended conformations.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00200f-ga.gif"/&gt;
	&lt;/p&gt;Jing Jiang, Morris M. Slutsky, Ticora V. Jones, Gregory N. Tew &lt;br/&gt;
(Paper from New J. Chem.)&lt;br/&gt;
Jing Jiang, New J. Chem., 2010, DOI: 10.1039/b9nj00200f&lt;br/&gt;
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		<dc:title>Apolar ortho-phenylene ethynylene oligomers: conformational ordering without intermolecular aggregation</dc:title>
		<dc:creator>Jing Jiang</dc:creator>
		<dc:creator>Morris M. Slutsky </dc:creator><dc:creator>Ticora V. Jones </dc:creator><dc:creator>Gregory N. Tew </dc:creator><dc:identifier>10.1039/b9nj00200f</dc:identifier>
		<dc:source>New J. Chem., 2010, DOI: 10.1039/b9nj00200f</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/b9nj00200f</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9nj00501c&amp;RSS=1"><title>Electron transfer from wheel to axle in a rotaxane. A mass spectrometric investigation</title>
		<link>http://xlink.rsc.org/?DOI=b9nj00501c&amp;RSS=1</link>
		<description>Electron transfer processes from the anthracene-based wheel to the viologen-based axle have been investigated in a new rotaxane and in related unthreaded and pseudo-rotaxanic adducts by a MS/MS CID technique.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00501c-ga.gif"/&gt;
	&lt;/p&gt;Sara Pasquale, Stefano Di Stefano, Bernardo Masci &lt;br/&gt;
(Paper from New J. Chem.)&lt;br/&gt;
Sara Pasquale, New J. Chem., 2010, DOI: 10.1039/b9nj00501c&lt;br/&gt;
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		<dc:title>Electron transfer from wheel to axle in a rotaxane. A mass spectrometric investigation</dc:title>
		<dc:creator>Sara Pasquale</dc:creator>
		<dc:creator>Stefano Di Stefano </dc:creator><dc:creator>Bernardo Masci </dc:creator><dc:identifier>10.1039/b9nj00501c</dc:identifier>
		<dc:source>New J. Chem., 2010, DOI: 10.1039/b9nj00501c</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/b9nj00501c</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9nj00234k&amp;RSS=1"><title>Supramolecular networks of a H-shaped aromatic phenol host</title>
		<link>http://xlink.rsc.org/?DOI=b9nj00234k&amp;RSS=1</link>
		<description>Solvents and cocrystal formers give a variety of hydrogen bond network architectures to a H-shaped tetraphenol tecton, notably novel examples of interpenetrated ladders, pentagonal Catalan nets, interpenetration and catenation in hexagonal (6,3) nets, and polyrotaxane threading.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00234k-ga.gif"/&gt;
	&lt;/p&gt;Ranjit Thakuria, Bipul Sarma, Ashwini Nangia &lt;br/&gt;
(Paper from New J. Chem.)&lt;br/&gt;
Ranjit Thakuria, New J. Chem., 2010, DOI: 10.1039/b9nj00234k&lt;br/&gt;
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		<dc:title>Supramolecular networks of a H-shaped aromatic phenol host</dc:title>
		<dc:creator>Ranjit Thakuria</dc:creator>
		<dc:creator>Bipul Sarma </dc:creator><dc:creator>Ashwini Nangia </dc:creator><dc:identifier>10.1039/b9nj00234k</dc:identifier>
		<dc:source>New J. Chem., 2010, DOI: 10.1039/b9nj00234k</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/b9nj00234k</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9nj00442d&amp;RSS=1"><title>Multisignaling detection of cyanide anions based on an iridium(iii) complex: remarkable enhancement of sensitivity by coordination effect</title>
		<link>http://xlink.rsc.org/?DOI=b9nj00442d&amp;RSS=1</link>
		<description>A novel iridium(iii) complex, 2, was synthesized, which was a specific lumino-chromo-electro chemodosimeter for cyanide anions, and is a much faster detector of cyanide anions than 1.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00442d-ga.gif"/&gt;
	&lt;/p&gt;Bin Lou, Zhu-Qi Chen, Zu-Qiang Bian, Chun-Hui Huang &lt;br/&gt;
(Paper from New J. Chem.)&lt;br/&gt;
Bin Lou, New J. Chem., 2010, DOI: 10.1039/b9nj00442d&lt;br/&gt;
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		<dc:title>Multisignaling detection of cyanide anions based on an iridium(iii) complex: remarkable enhancement of sensitivity by coordination effect</dc:title>
		<dc:creator>Bin Lou</dc:creator>
		<dc:creator>Zhu-Qi Chen </dc:creator><dc:creator>Zu-Qiang Bian </dc:creator><dc:creator>Chun-Hui Huang </dc:creator><dc:identifier>10.1039/b9nj00442d</dc:identifier>
		<dc:source>New J. Chem., 2010, DOI: 10.1039/b9nj00442d</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/b9nj00442d</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9nj00452a&amp;RSS=1"><title>A kinetic investigation, supported by theoretical calculations, of steric and ring strain effects on the oxidation of sulfides and sulfoxides by dimethyldioxirane in acetone</title>
		<link>http://xlink.rsc.org/?DOI=b9nj00452a&amp;RSS=1</link>
		<description>The oxidations of sulfides and sulfoxides by dimethyldioxirane in acetone exhibit contrasting sensitivities to steric and ring strain effects.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00452a-ga.gif"/&gt;
	&lt;/p&gt;Peter Hanson, Ramon A. A. J. Hendrickx, John R. Lindsay Smith &lt;br/&gt;
(Paper from New J. Chem.)&lt;br/&gt;
Peter Hanson, New J. Chem., 2010, DOI: 10.1039/b9nj00452a&lt;br/&gt;
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		<dc:title>A kinetic investigation, supported by theoretical calculations, of steric and ring strain effects on the oxidation of sulfides and sulfoxides by dimethyldioxirane in acetone</dc:title>
		<dc:creator>Peter Hanson</dc:creator>
		<dc:creator>Ramon A. A. J. Hendrickx </dc:creator><dc:creator>John R. Lindsay Smith </dc:creator><dc:identifier>10.1039/b9nj00452a</dc:identifier>
		<dc:source>New J. Chem., 2010, DOI: 10.1039/b9nj00452a</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/b9nj00452a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9nj00399a&amp;RSS=1"><title>Silica nanoparticles as a reusable catalyst: a straightforward route for the synthesis of thioethers, thioesters, vinyl thioethers and thio-Michael adducts under neutral reaction conditions</title>
		<link>http://xlink.rsc.org/?DOI=b9nj00399a&amp;RSS=1</link>
		<description>A simple and straightforward route for the synthesis of thioethers, thioesters, vinyl thioethers and thio-Michael adducts has been demonstrated using free silica nanoparticles as a reusable catalyst via the 1,2-addition of thiols to alkenes, alkynes and alkyl/acyl halides, and the 1,4-addition of thiols to conjugated alkenes at room temperature.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00399a-ga.gif"/&gt;
	&lt;/p&gt;Subhash Banerjee, Jayanta Das, Richard P. Alvarez, Swadeshmukul Santra &lt;br/&gt;
(Paper from New J. Chem.)&lt;br/&gt;
Subhash Banerjee, New J. Chem., 2010, DOI: 10.1039/b9nj00399a&lt;br/&gt;
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		<dc:title>Silica nanoparticles as a reusable catalyst: a straightforward route for the synthesis of thioethers, thioesters, vinyl thioethers and thio-Michael adducts under neutral reaction conditions</dc:title>
		<dc:creator>Subhash Banerjee</dc:creator>
		<dc:creator>Jayanta Das </dc:creator><dc:creator>Richard P. Alvarez </dc:creator><dc:creator>Swadeshmukul Santra </dc:creator><dc:identifier>10.1039/b9nj00399a</dc:identifier>
		<dc:source>New J. Chem., 2010, DOI: 10.1039/b9nj00399a</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/b9nj00399a</dc:identifier>
	</item>
</rdf:RDF>
