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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.
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