Electrochemical Synthesis of Cobalt Complexes with 4‐Methyl‐N‐(2‐pyridylmethyl)benzenesulfonamide (HL) − Crystal Structures of HL, [CoIIL2] and [CoIIIL2Lo] [Lo = {HNC(CH3)}2C(CN)]
Electrochemical Synthesis of Cobalt Complexes with 4‐Methyl‐N‐(2‐pyridylmethyl)benzenesulfonamide (HL) − Crystal Structures of HL, [CoIIL2] and [CoIIIL2Lo] [Lo = {HNC(CH3)}2C(CN)]
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电化学合成 4-甲基-N-(2-吡啶甲基)苯磺酰胺 (HL) 钴络合物 - HL、[CoIIL2] 和 [CoIIIL2Lo] 的晶体结构 [Lo = {HNC(CH3)}2C(CN)]
DOI:
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发表时间:
2002
期刊:
影响因子:
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通讯作者:
A. Sousa
中科院分区:
文献类型:
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作者:
M. L. Durán;J. García;Cristina Gómez;A. Sousa;J. Romero;A. Sousa
Electrochemical oxidation of cobalt in a solution of 4-methyl-N-(2-pyridylmethyl)benzenesulfonamide (HL, 1) in acetonitrile afforded the compounds [CoIIL2] (2) or [CoIIIL2Lo] (3). When 2,2′-bipyridine (bipy) or 1,10-phenanthroline (phen) was added to the electrolytic phase, [CoIIL2bipy] (4) and [CoIIL2phen] (5) were obtained. The crystal structures of HL (1), [CoIIL2] (2) and [CoIIIL2Lo] (3) were determined by X-ray diffraction techniques. The compound [CoIIL2] is mononuclear and has a distorted tetrahedral [CoN4] geometry, with each amide ligand acting as an anionic (NamideNpy) bidentate ligand. In the monomeric complex [CoIIIL2Lo] the cobalt atom is in a distorted octahedral [CoN6] environment defined by the amide and pyridyl nitrogen atoms of two L− anionic ligands and the two nitrogen atoms of the NH groups of a new anionic ligand Lo, which is formed by trimerisation of three acetonitrile molecules in the electrolytic cell. The electronic, IR and FAB spectra of the compounds are discussed. (© Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002)