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Crystal structures and thermal behavior of complexes of group 13 metal halides with pyridine-type ligands

机译:十三族金属卤化物与吡啶型配体的配合物的晶体结构和热行为

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摘要

Complexes of group 13 metal halides with pyridine-type ligands (pyridine, pyrazine, and 4,4'-bipyridine) have molecular, polymeric, or ionic structures containing metal atoms with a coordination number of 4, 5, or 6 depending on the component ratio, the acceptor ability of the halide, the donor ability and the coordination mode of the ligand. The strongest donor-acceptor bond is formed in the 1 : 1 molecular complexes, and their transition to the gas phase is energetically most favorable. The acceptor ability of Lewis acids in the complexes decreases in the series AlCl3 > AlBr3 > GaCl3 > GaBr3 > GaI3. The stability of the complexes with respect to homogeneous dissociation correlates with the donor proton affinity. Group 13 metal trihalides act as catalysts for the pyrolysis of ligands.
机译:具有吡啶型配体(吡啶,吡嗪和4,4'-联吡啶)的第13组金属卤化物的配合物具有分子,聚合物或离子结构,其中包含根据成分而定的金属原子数为4、5或6的金属原子比率,卤化物的受体能力,供体能力和配体的配位方式。最强的供体-受体键是在1:1分子复合物中形成的,从能量上讲,它们向气相的转变是最有利的。络合物中路易斯酸的受体能力按AlCl3> AlBr3> GaCl3> GaBr3> GaI3的顺序降低。复合物相对于均质解离的稳定性与供体质子亲和力相关。 13族金属三卤化物用作配体热解的催化剂。

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