RSC - New J. Chem. latest articles http://xlink.rsc.org/jumptojournal.cfm?journal_code=NJ The Royal Society of Chemistry en-gb Copyright (c) 2010 The Royal Society of Chemistry New J. Chem. Copyright (c) The Royal Society of Chemistry contracts-copyright@rsc.org 1144-05461369-9261The Royal Society of Chemistry The Royal Society of Chemistry Royal Society of Chemistry - New J. Chem. latest articles RSC - New J. Chem. latest articles http://www.rsc.org text/html text http://xlink.rsc.org/?DOI=b9nj00218a&RSS=1 The inclusion complex of DMC@CB[8] shows a sexfoil packing structure compared to the aligned structure in the free cucurbit[8]uril.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00218a-ga.gif"/> </p>Wu Xiao-jun, Hu Kai, Meng Xiang-gao, Cheng Gong-zhen <br/> (Letter from New J. Chem.)<br/> Wu Xiao-jun, New J. Chem., 2010, DOI: 10.1039/b9nj00218a<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry A cucurbit[8]uril inclusion complex with 1,7-dimethyl-1,4,7,10-tetraazacyclododecane tetrachloride Wu Xiao-jun Hu Kai Meng Xiang-gao Cheng Gong-zhen 10.1039/b9nj00218a New J. Chem., 2010, DOI: 10.1039/b9nj00218a html/pdf 2009-11-27 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00218a http://xlink.rsc.org/?DOI=b9nj00588a&RSS=1 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.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00588a-ga.gif"/> </p>Oleksandr Dolotko, Jerzy W. Wiench, Kevin W. Dennis, Vitalij K. Pecharsky, Viktor P. Balema <br/> (Letter from New J. Chem.)<br/> Oleksandr Dolotko, New J. Chem., 2010, DOI: 10.1039/b9nj00588a<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry Mechanically induced reactions in organic solids: liquid eutectics or solid-state processes? Oleksandr Dolotko Jerzy W. Wiench Kevin W. Dennis Vitalij K. Pecharsky Viktor P. Balema 10.1039/b9nj00588a New J. Chem., 2010, DOI: 10.1039/b9nj00588a html/pdf 2009-11-24 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00588a http://xlink.rsc.org/?DOI=b9nj00355j&RSS=1 Crystal structures of new Na5Ag2Fe3(As2O7)4 and Na2Ag5Fe3(P2O7)4 compounds are reported.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00355j-ga.gif"/> </p>Eric Quarez, Olivier Mentre, Karim Djellab, Christian Masquelier <br/> (Paper from New J. Chem.)<br/> Eric Quarez, New J. Chem., 2010, DOI: 10.1039/b9nj00355j<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry Crystal structures and sodium/silver distributions within the ionic conductors Na5Ag2Fe3(As2O7)4 and Na2Ag5Fe3(P2O7)4 Eric Quarez Olivier Mentre Karim Djellab Christian Masquelier 10.1039/b9nj00355j New J. Chem., 2010, DOI: 10.1039/b9nj00355j html/pdf 2009-11-24 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00355j http://xlink.rsc.org/?DOI=b9nj00277d&RSS=1 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.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00277d-ga.gif"/> </p>Sanjay Singh, V. D'Britto, A. A. Prabhune, C. V. Ramana, Alok Dhawan, B. L. V. Prasad <br/> (Paper from New J. Chem.)<br/> Sanjay Singh, New J. Chem., 2010, DOI: 10.1039/b9nj00277d<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry Cytotoxic and genotoxic assessment of glycolipid-reduced and -capped gold and silver nanoparticles Sanjay Singh V. D'Britto A. A. Prabhune C. V. Ramana Alok Dhawan B. L. V. Prasad 10.1039/b9nj00277d New J. Chem., 2010, DOI: 10.1039/b9nj00277d html/pdf 2009-11-24 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00277d http://xlink.rsc.org/?DOI=b9nj00200f&RSS=1 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.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00200f-ga.gif"/> </p>Jing Jiang, Morris M. Slutsky, Ticora V. Jones, Gregory N. Tew <br/> (Paper from New J. Chem.)<br/> Jing Jiang, New J. Chem., 2010, DOI: 10.1039/b9nj00200f<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry Apolar ortho-phenylene ethynylene oligomers: conformational ordering without intermolecular aggregation Jing Jiang Morris M. Slutsky Ticora V. Jones Gregory N. Tew 10.1039/b9nj00200f New J. Chem., 2010, DOI: 10.1039/b9nj00200f html/pdf 2009-11-24 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00200f http://xlink.rsc.org/?DOI=b9nj00501c&RSS=1 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.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00501c-ga.gif"/> </p>Sara Pasquale, Stefano Di Stefano, Bernardo Masci <br/> (Paper from New J. Chem.)<br/> Sara Pasquale, New J. Chem., 2010, DOI: 10.1039/b9nj00501c<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry Electron transfer from wheel to axle in a rotaxane. A mass spectrometric investigation Sara Pasquale Stefano Di Stefano Bernardo Masci 10.1039/b9nj00501c New J. Chem., 2010, DOI: 10.1039/b9nj00501c html/pdf 2009-11-24 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00501c http://xlink.rsc.org/?DOI=b9nj00234k&RSS=1 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.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00234k-ga.gif"/> </p>Ranjit Thakuria, Bipul Sarma, Ashwini Nangia <br/> (Paper from New J. Chem.)<br/> Ranjit Thakuria, New J. Chem., 2010, DOI: 10.1039/b9nj00234k<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry Supramolecular networks of a H-shaped aromatic phenol host Ranjit Thakuria Bipul Sarma Ashwini Nangia 10.1039/b9nj00234k New J. Chem., 2010, DOI: 10.1039/b9nj00234k html/pdf 2009-11-23 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00234k http://xlink.rsc.org/?DOI=b9nj00442d&RSS=1 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.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00442d-ga.gif"/> </p>Bin Lou, Zhu-Qi Chen, Zu-Qiang Bian, Chun-Hui Huang <br/> (Paper from New J. Chem.)<br/> Bin Lou, New J. Chem., 2010, DOI: 10.1039/b9nj00442d<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry Multisignaling detection of cyanide anions based on an iridium(iii) complex: remarkable enhancement of sensitivity by coordination effect Bin Lou Zhu-Qi Chen Zu-Qiang Bian Chun-Hui Huang 10.1039/b9nj00442d New J. Chem., 2010, DOI: 10.1039/b9nj00442d html/pdf 2009-11-20 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00442d http://xlink.rsc.org/?DOI=b9nj00452a&RSS=1 The oxidations of sulfides and sulfoxides by dimethyldioxirane in acetone exhibit contrasting sensitivities to steric and ring strain effects.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2009/b9nj00452a-ga.gif"/> </p>Peter Hanson, Ramon A. A. J. Hendrickx, John R. Lindsay Smith <br/> (Paper from New J. Chem.)<br/> Peter Hanson, New J. Chem., 2009, DOI: 10.1039/b9nj00452a<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry A kinetic investigation, supported by theoretical calculations, of steric and ring strain effects on the oxidation of sulfides and sulfoxides by dimethyldioxirane in acetone Peter Hanson Ramon A. A. J. Hendrickx John R. Lindsay Smith 10.1039/b9nj00452a New J. Chem., 2009, DOI: 10.1039/b9nj00452a html/pdf 2009-11-17 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00452a http://xlink.rsc.org/?DOI=b9nj00399a&RSS=1 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.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00399a-ga.gif"/> </p>Subhash Banerjee, Jayanta Das, Richard P. Alvarez, Swadeshmukul Santra <br/> (Paper from New J. Chem.)<br/> Subhash Banerjee, New J. Chem., 2010, DOI: 10.1039/b9nj00399a<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry 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 Subhash Banerjee Jayanta Das Richard P. Alvarez Swadeshmukul Santra 10.1039/b9nj00399a New J. Chem., 2010, DOI: 10.1039/b9nj00399a html/pdf 2009-11-16 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00399a http://xlink.rsc.org/?DOI=b9nj00486f&RSS=1 Two protocols based on Cu(i) template synthesis and "click" reactions for the synthesis of functionalized macrocycles and [2]catenanes are described. The introduction of peripheral functional groups into the catenane structure opens up possibilities of using these materials as building blocks for preparation of even more complex structures.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2010/b9nj00486f-ga.gif"/> </p>Jackson D. Megiatto, Jr., David I. Schuster <br/> (Paper from New J. Chem.)<br/> Jackson D. Megiatto, Jr., New J. Chem., 2010, DOI: 10.1039/b9nj00486f<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry Introduction of useful peripheral functional groups on [2]catenanes by combining Cu(i) template synthesis with "click" chemistry Jackson D. Megiatto, Jr. David I. Schuster 10.1039/b9nj00486f New J. Chem., 2010, DOI: 10.1039/b9nj00486f html/pdf 2009-11-11 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00486f http://xlink.rsc.org/?DOI=b9nj00474b&RSS=1 Flash vacuum pyrolysis (FVP) of the aminopyridazinone derivatives of Meldrum's acid at 600 [degree]C (0.02 Torr) results in generation of an imidoylketene intermediate followed by cyclisation. The 4-amino compounds shown lead to mixtures of pyrido[2,3-d]pyridazines and pyrrolo[3,2-c]pyridazines. A suggested mechanism for the formation of the latter is supported by DFT calculations.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2009/b9nj00474b-ga.gif"/> </p>Alexander P. Gaywood, Lawrence Hill, S. Haider Imam, Hamish McNab, Gabor Neumajer, William J. O'Neill, Peter Matyus <br/> (Paper from New J. Chem.)<br/> Alexander P. Gaywood, New J. Chem., 2009, DOI: 10.1039/b9nj00474b<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry Cyclisation reactions of some pyridazinylimidoylketenes Alexander P. Gaywood Lawrence Hill S. Haider Imam Hamish McNab Gabor Neumajer William J. O'Neill Peter Matyus 10.1039/b9nj00474b New J. Chem., 2009, DOI: 10.1039/b9nj00474b html/pdf 2009-11-10 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00474b http://xlink.rsc.org/?DOI=b9nj00314b&RSS=1 A new heterogenized catalyst of a sulfonato-salen-nickel(ii) complex immobilized on a layered double hydroxide host has been synthesized and characterized through various spectroscopic and microscopic techniques. The catalytic properties of the catalyst were examined in liquid phase tetralin oxidation.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2009/b9nj00314b-ga.gif"/> </p>Samiran Bhattacharjee, Kwang-Eun Jeong, Soon-Yong Jeong, Wha-Seung Ahn <br/> (Paper from New J. Chem.)<br/> Samiran Bhattacharjee, New J. Chem., 2009, DOI: 10.1039/b9nj00314b<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry Synthesis of a sulfonato-salen-nickel(ii) complex immobilized in LDH for tetralin oxidation Samiran Bhattacharjee Kwang-Eun Jeong Soon-Yong Jeong Wha-Seung Ahn 10.1039/b9nj00314b New J. Chem., 2009, DOI: 10.1039/b9nj00314b html/pdf 2009-11-05 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00314b http://xlink.rsc.org/?DOI=b9nj00400a&RSS=1 A series of 4,6-O-protected-N-glycosylamine-based organogelators were synthesised and characterized. The existence of [small pi]-[small pi] stacking, dipole-dipole interactions and H-bonding were inferred from 1H NMR, FT-IR, XRD and computational studies. The gelation properties were studied in regard to their molecular structure by various techniques.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2009/b9nj00400a-ga.gif"/> </p>Subbiah Nagarajan, Pawar Ravinder, Venkatesan Subramanian, Thangamuthu Mohan Das <br/> (Paper from New J. Chem.)<br/> Subbiah Nagarajan, New J. Chem., 2009, DOI: 10.1039/b9nj00400a<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry Protecting group/halogen effect of N-glycosylamines on the self assembly of organogelator Subbiah Nagarajan Pawar Ravinder Venkatesan Subramanian Thangamuthu Mohan Das 10.1039/b9nj00400a New J. Chem., 2009, DOI: 10.1039/b9nj00400a html/pdf 2009-11-05 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00400a http://xlink.rsc.org/?DOI=b9nj00307j&RSS=1 A simple surface-active ATRP initiator was synthesized efficiently. Living/controlled radical emulsion polymerization of methyl methacrylate was realized under ARGET ATRP conditions, in which the new initiator functioned as both an ATRP initiator and a latex stabilizer.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2009/b9nj00307j-ga.gif"/> </p>Chuanjie Cheng, Jinbing Shu, Shanshan Gong, Liang Shen, Yongluo Qiao, Changqing Fu <br/> (Paper from New J. Chem.)<br/> Chuanjie Cheng, New J. Chem., 2009, DOI: 10.1039/b9nj00307j<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry Synthesis and use of a surface-active initiator in emulsion polymerization under AGET and ARGET ATRP conditions Chuanjie Cheng Jinbing Shu Shanshan Gong Liang Shen Yongluo Qiao Changqing Fu 10.1039/b9nj00307j New J. Chem., 2009, DOI: 10.1039/b9nj00307j html/pdf 2009-11-05 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00307j http://xlink.rsc.org/?DOI=b908915b&RSS=1 The nuclear and electronic densities of the short intramolecular hydrogen bond in dibenzoylmethane show an asymmetric proton position, accompanied by a migration of the hydrogen bonding electron density from asymmetric at low temperature to almost centred at room temperature.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2009/b908915b-ga.gif"/> </p>Lynne H. Thomas, Alastair J. Florence, Chick C. Wilson <br/> (Paper from New J. Chem.)<br/> Lynne H. Thomas, New J. Chem., 2009, 33, 2486 <br/>DOI: 10.1039/b908915b <br/>The content of this RSS Feed (c) The Royal Society of Chemistry Hydrogen atom behaviour imaged in a short intramolecular hydrogen bond using the combined approach of X-ray and neutron diffraction Lynne H. Thomas Alastair J. Florence Chick C. Wilson 10.1039/b908915b New J. Chem., 2009, 33, 2486 DOI: 10.1039/b908915b html/pdf 2009-11-04 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b908915b 33122486 http://xlink.rsc.org/?DOI=b9nj00380k&RSS=1 A novel dendritic light harvester, synthesized by coupling convergent dendrimer synthesis with click chemistry, has eight BODIPY units at the periphery and a perylenediimide (PDI) chromophore at the core.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2009/b9nj00380k-ga.gif"/> </p>O. Altan Bozdemir, M. Deniz Yilmaz, Onur Buyukcakir, Aleksander Siemiarczuk, Mehmet Tutas, Engin U. Akkaya <br/> (Paper from New J. Chem.)<br/> O. Altan Bozdemir, New J. Chem., 2009, DOI: 10.1039/b9nj00380k<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry Convergent synthesis and light harvesting properties of dendritic boradiazaindacene (BODIPY) appended perylenediimide dyes O. Altan Bozdemir M. Deniz Yilmaz Onur Buyukcakir Aleksander Siemiarczuk Mehmet Tutas Engin U. Akkaya 10.1039/b9nj00380k New J. Chem., 2009, DOI: 10.1039/b9nj00380k html/pdf 2009-11-03 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00380k http://xlink.rsc.org/?DOI=b9nj00465c&RSS=1 [Ru(bpy)2(dpb)]2+ exhibits very long wavelength 1MLCT absorption, with a maximum at 550 nm, and DNA photocleavage activity in anaerobic conditions in the presence of suitable oxidative quenchers.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2009/b9nj00465c-ga.gif"/> </p>Qian-Xiong Zhou, Wan-Hua Lei, Chao Li, Yuan-Jun Hou, Xue-Song Wang, Bao-Wen Zhang <br/> (Paper from New J. Chem.)<br/> Qian-Xiong Zhou, New J. Chem., 2009, DOI: 10.1039/b9nj00465c<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry DNA photocleavage in anaerobic conditions by a Ru(ii) polypyridyl complex with long wavelength MLCT absorption Qian-Xiong Zhou Wan-Hua Lei Chao Li Yuan-Jun Hou Xue-Song Wang Bao-Wen Zhang 10.1039/b9nj00465c New J. Chem., 2009, DOI: 10.1039/b9nj00465c html/pdf 2009-11-02 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00465c http://xlink.rsc.org/?DOI=b9nj00372j&RSS=1 The bromination of 2,3-dicarbomethoxy- and 2,3-dicyano benzobarrelene at different temperatures was investigated and a possible role of substituents on the bromination reaction was discussed.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2009/b9nj00372j-ga.gif"/> </p>Sara Taskesenlioglu, Arif Dastan, Erdin Dalk[i without dot]l[i without dot]c, Murat Guney, Rza Abbasoglu <br/> (Paper from New J. Chem.)<br/> Sara Taskesenlioglu, New J. Chem., 2009, DOI: 10.1039/b9nj00372j<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry Low and high temperature bromination of 2,3-dicarbomethoxy and 2,3-dicyano benzobarrelene: unexpected substituent effect on bromination Sara Taskesenlioglu Arif Dastan Erdin Dalk[i without dot]l[i without dot]c Murat Guney Rza Abbasoglu 10.1039/b9nj00372j New J. Chem., 2009, DOI: 10.1039/b9nj00372j html/pdf 2009-11-02 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00372j