首页> 外文期刊>Russian Journal of General Chemistry >Molecular Complexes of mu-Carbidodimeric Iron(IV) Tetra-4-tert-butylphthalocyaninate with Nitrogenous Bases
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Molecular Complexes of mu-Carbidodimeric Iron(IV) Tetra-4-tert-butylphthalocyaninate with Nitrogenous Bases

机译:Mu-碳化二聚体铁(iv)四-4-叔丁基酞用含氮碱基的分子复合物

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摘要

The reaction of mu-carbidodimeric iron(IV) tetra-4-tert-butylphthalocyaninate with nitrogenous bases (imidazole and its derivatives, pyridine, diethylamine), which involves formation of donoraEuro'acceptor complexes with a preserved dimeric structure, was studied by spectral methods. The composition of such molecular complexes and their comparative stability were determined. The coordination power of mu- carbidodimeric iron(IV) tetra-4-tert-butylphthalocyaninate was found to depend on the nature of the nitrogenous base and macrocycle. Quantum-chemical modeling of the coordination reaction was performed. The energetic and geometric characteristics of the donoraEuro'acceptor complexes were obtained. The composition of the reaction products was shown to be affected of the degree of deformation of the macrocycle.
机译:通过光谱方法研究了含有含氮碱(咪唑及其衍生物,吡啶,吡啶,二乙胺)与含氮碱(咪唑及其衍生物,吡啶,二乙胺)的反应,这涉及形成Donoraeuro'accepcor络合物的唐毒素的络合物 。 确定这些分子复合物的组成及其对比稳定性。 发现MU-碳化二聚体铁(IV)Tetra-4-叔丁基酞菁的配位力取决于含氮基础和宏循环的性质。 进行配位反应的量子化学建模。 获得了Donoraeuro'acceptor络合物的能量和几何特征。 显示反应产物的组成被显示为宏循环变形程度的影响。

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