RSC - New J. Chem. latest articles 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 Multisignaling detection of cyanide anions based on an iridium(iii) complex: remarkable enhancement of sensitivity by coordination effect 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 A kinetic investigation, supported by theoretical calculations, of steric and ring strain effects on the oxidation of sulfides and sulfoxides by dimethyldioxirane in acetone 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 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 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 Introduction of useful peripheral functional groups on [2]catenanes by combining Cu(i) template synthesis with "click" chemistry 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 Cyclisation reactions of some pyridazinylimidoylketenes 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 Synthesis of a sulfonato-salen-nickel(ii) complex immobilized in LDH for tetralin oxidation 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 Protecting group/halogen effect of N-glycosylamines on the self assembly of organogelator 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 Synthesis and use of a surface-active initiator in emulsion polymerization under AGET and ARGET ATRP conditions 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 Hydrogen atom behaviour imaged in a short intramolecular hydrogen bond using the combined approach of X-ray and neutron diffraction 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, DOI: 10.1039/b908915b<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 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, 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 Convergent synthesis and light harvesting properties of dendritic boradiazaindacene (BODIPY) appended perylenediimide dyes 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 DNA photocleavage in anaerobic conditions by a Ru(ii) polypyridyl complex with long wavelength MLCT absorption 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 Low and high temperature bromination of 2,3-dicarbomethoxy and 2,3-dicyano benzobarrelene: unexpected substituent effect on bromination 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 A sugar-pyrene-based fluorescent gelator: nanotubular architecture and interaction with SWCNTs http://xlink.rsc.org/?DOI=b9nj00395a&RSS=1 A sugar-pyrene-based fluorescent gelator was synthesised and characterized based on different spectral techniques. The weak interactions that exist between the pyrene moieties are responsible for gelation, which is absent in case of functionalised SWCNTs.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2009/b9nj00395a-ga.gif"/> </p>Subbiah Nagarajan, Thangamuthu Mohan Das <br/> (Letter from New J. Chem.)<br/> Subbiah Nagarajan, New J. Chem., 2009, DOI: 10.1039/b9nj00395a<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 sugar-pyrene-based fluorescent gelator: nanotubular architecture and interaction with SWCNTs Subbiah Nagarajan Thangamuthu Mohan Das 10.1039/b9nj00395a New J. Chem., 2009, DOI: 10.1039/b9nj00395a html/pdf 2009-10-30 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00395a Synthesis and characterization of a highly stable dendritic catechol-tripod bearing technetium-99m http://xlink.rsc.org/?DOI=b9nj00305c&RSS=1 A dendritic 99mTc ligand 1 derived from a pre-organized tripodal tris-catecholamide exhibits a kinetic stability by far more important than its corresponding diethylenetriamine pentaacetic acid homologue 2.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2009/b9nj00305c-ga.gif"/> </p>Annabelle Bertin, Anne-Isabelle Michou-Gallani, Jerome Steibel, Jean-Louis Gallani, Delphine Felder-Flesch <br/> (Paper from New J. Chem.)<br/> Annabelle Bertin, New J. Chem., 2009, DOI: 10.1039/b9nj00305c<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 characterization of a highly stable dendritic catechol-tripod bearing technetium-99m Annabelle Bertin Anne-Isabelle Michou-Gallani Jerome Steibel Jean-Louis Gallani Delphine Felder-Flesch 10.1039/b9nj00305c New J. Chem., 2009, DOI: 10.1039/b9nj00305c html/pdf 2009-10-29 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00305c The synthesis of novel core-substituted naphthalene diimides via Suzuki cross-coupling and their properties http://xlink.rsc.org/?DOI=b9nj00476a&RSS=1 Suzuki cross-coupling reactions were invented for the core-substitution of 2,6-dihalonaphthalene diimides with arylboronic acids. The aryl substituents at the 2,6-positions red-shift the absorbance and enhance the fluorescence of the naphthalene diimides, making them useful electroactive elements for supramolecular materials.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2009/b9nj00476a-ga.gif"/> </p>Sheshanath V. Bhosale, Mohan B. Kalyankar, Sidhanath V. Bhosale, Steven J. Langford, Ellen F. Reid, Conor F. Hogan <br/> (Letter from New J. Chem.)<br/> Sheshanath V. Bhosale, New J. Chem., 2009, DOI: 10.1039/b9nj00476a<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 The synthesis of novel core-substituted naphthalene diimides via Suzuki cross-coupling and their properties Sheshanath V. Bhosale Mohan B. Kalyankar Sidhanath V. Bhosale Steven J. Langford Ellen F. Reid Conor F. Hogan 10.1039/b9nj00476a New J. Chem., 2009, DOI: 10.1039/b9nj00476a html/pdf 2009-10-28 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00476a From ill-resolved atomic to ZSM-5 type of ordering in mesoporous lamellar aluminosilica nanoparticles http://xlink.rsc.org/?DOI=b9nj00331b&RSS=1 Ill-resolved atomic and ZSM-5 types of ordering in mesostructured nanoparticles are obtained using a cationic and anionic surfactant mixture as a template and TPA+ as a structure directing agent.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2009/b9nj00331b-ga.gif"/> </p>Kun Zhang, Yi Meng Wang, Belen Albela, Li Chen, Ming-Yuan He, Laurent Bonneviot <br/> (Paper from New J. Chem.)<br/> Kun Zhang, New J. Chem., 2009, DOI: 10.1039/b9nj00331b<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 From ill-resolved atomic to ZSM-5 type of ordering in mesoporous lamellar aluminosilica nanoparticles Kun Zhang Yi Meng Wang Belen Albela Li Chen Ming-Yuan He Laurent Bonneviot 10.1039/b9nj00331b New J. Chem., 2009, DOI: 10.1039/b9nj00331b html/pdf 2009-10-28 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00331b Oxoanion binding: a change of selectivity for porphyrin-alkaloid conjugates as a result of substitution pattern http://xlink.rsc.org/?DOI=b9nj00387h&RSS=1 The selective interaction of two porphyrin-brucine quaternary salts with oxoanions in a methanol/aqueous environment is described.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2009/b9nj00387h-ga.gif"/> </p>Lenka Veverkova, Kamil Zaruba, Jitka Koukolova, Vladimir Kral <br/> (Paper from New J. Chem.)<br/> Lenka Veverkova, New J. Chem., 2009, DOI: 10.1039/b9nj00387h<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 Oxoanion binding: a change of selectivity for porphyrin-alkaloid conjugates as a result of substitution pattern Lenka Veverkova Kamil Zaruba Jitka Koukolova Vladimir Kral 10.1039/b9nj00387h New J. Chem., 2009, DOI: 10.1039/b9nj00387h html/pdf 2009-10-26 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00387h The effect of different ligand substituents on the chemistry of a zinc-pyrazole anion host http://xlink.rsc.org/?DOI=b9nj00412b&RSS=1 [ZnCl(HpzCy)3]NO3 (HpzCy = 5-cyclohexylpyrazole) forms dimeric hydrogen-bonded capsules containing two nitrate anions (shown). In contrast, [ZnBr(HpzCy)3]NO3[middle dot]H2O contains chains of anions and water molecules lying within channels formed by the cations.<p><img align="center" src="http://www.rsc.org/ejga/NJ/2009/b9nj00412b-ga.gif"/> </p>Jonathan Day, Katie E. R. Marriott, Colin A. Kilner, Malcolm A. Halcrow <br/> (Paper from New J. Chem.)<br/> Jonathan Day, New J. Chem., 2009, DOI: 10.1039/b9nj00412b<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 The effect of different ligand substituents on the chemistry of a zinc-pyrazole anion host Jonathan Day Katie E. R. Marriott Colin A. Kilner Malcolm A. Halcrow 10.1039/b9nj00412b New J. Chem., 2009, DOI: 10.1039/b9nj00412b html/pdf 2009-10-26 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b9nj00412b