首页> 外文期刊>Inorganica Chimica Acta >Synthesis, characterization and structure of ruthenium(II) phosphine complexes with N-heterocyclic thiolate ligands
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Synthesis, characterization and structure of ruthenium(II) phosphine complexes with N-heterocyclic thiolate ligands

机译:N-杂环硫醇盐配体的钌(II)膦配合物的合成,表征和结构

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The [Ru(dppb)(mbt)(2)], mbt = 2-mercaptobenzothiazole, complex, isolated from the reaction of the mer-[RuCl3(dppb)(OH,)] complex with the 2,2'-dithiobis(benzothiazole), mbts, was characterized by spectroscopic and electrochemical techniques (E-1/2 = 0.78 V versus NHE) and its structure was determined by crystal X-ray analysis. The structural analysis suggests that the S-S bond of the mbts ligand is cleaved, thus forming two four-membered chelate rings coordinated to the ruthenium through the N,S-donor atoms of the mbt reduced ligands, with an average bite angle of 67.295(11)degrees. The H-1 and C-13 NMR signals observed for mbts ligand coordinated to the metal center, the changes in the vibrational spectra, and the appearance of a MLCT band in the electronic spectrum of the complex point for the reduced state of the ruthenium metal center, Ru-II. These reducing processes are suggested to be due to the methanol interference, which is observed to be strongly affected by N-methylmorpholine. The cytochrome c electrochemistry was analyzed by using the SAMs formed by the mbts and the [Ru(dppb)(mbt)(2)] complex on gold, with only the former presenting electroactivity. (c) 2005 Elsevier B.V. All rights reserved.
机译:[Ru(dppb)(mbt)(2)],mbt = 2-巯基苯并噻唑,配合物,是从mer- [RuCl3(dppb)(OH,)]配合物与2,2'-二硫代双(通过光谱和电化学技术(E-1 / 2 = 0.78 V对NHE)表征了mbts(苯并噻唑)的结构,并通过晶体X射线分析确定了其结构。结构分析表明mbts配体的SS键断裂,从而形成两个通过mbt还原的配体的N,S供体原子与钌配位的四元螯合环,平均咬合角为67.295(11) )度。观察到的mbts配体的H-1和C-13 NMR信号与金属中心配位,振动光谱的变化以及在钌原子还原态的复数点电子光谱中MLCT带的出现中心,Ru-II。这些还原过程被认为是由于甲醇的干扰,据观察,它受到N-甲基吗啉的强烈影响。使用mbts和金上的[Ru(dppb)(mbt)(2)]络合物形成的SAM分析细胞色素c电化学,只有前者具有电活性。 (c)2005 Elsevier B.V.保留所有权利。

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