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首页> 外文期刊>Journal of Molecular Structure. Theochem: Applications of Theoretical Chemistry to Organic, Inorganic and Biological Problems >Electronic spectral determination of the heterocyclic nitrogen base adducts of nickel(II)-di(2,6-dichlorophenyl)carbazonate
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Electronic spectral determination of the heterocyclic nitrogen base adducts of nickel(II)-di(2,6-dichlorophenyl)carbazonate

机译:电子光谱测定镍(II)-二(2,6-二氯苯基)咔唑酸镍的杂环氮基加合物

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摘要

The ligand di(2,6-dichlorophenyl)carbazone (hereafter named as D2,6DClPC) and its nickel(II) complex have been synthesised and characterised by elemental analyses, magnetic moment and spectral measurements. The adduct formation constants of various heterocyclic nitrogen bases with nickel(II) chelates of D2,6DClPC have been determined in a monophase chloroform by electronic spectral study. Bathochromic and hypsochromic shifts were observed in the optical spectra in the visible range, due to adduct formation. The saturated monodentate bases such as pyrrolidine, piperidine, etc., form pentacoordinate adducts of 1:1 stoichiometry, whereas bidentate and unsaturated monodentate bases form hexacoordinated adducts with 1:1 metal-ligand stoichiometry. The experimental results are discussed in terms of steric properties, basicity and ring structures of the various heterocyclic bases.
机译:合成了配体二(2,6-二氯苯基)咔zone(以下称为D2,6DClPC)及其镍(II)配合物,并通过元素分析,磁矩和光谱测量对其进行了表征。在单相氯仿中通过电子光谱研究确定了各种杂环氮碱与D2,6DClPC的镍(II)螯合物的加合物形成常数。由于加合物的形成,在可见光范围内的光谱中观察到了红移和蓝移。饱和的单齿碱基,例如吡咯烷,哌啶等,形成化学计量比为1:1的五配位加合物,而二齿和不饱和单齿碱基形成金属配体为1:1的六配位加合物。从各种杂环碱基的空间性质,碱度和环结构方面讨论了实验结果。

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