第 13 组二硫代磷酸酯和二硫代磷酸酯的结构化学书目调查

Edward R. T. Tiekink
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引用次数: 0

摘要

本文介绍了经晶体学测定的第 13 组二硫代磷酸酯和二硫代磷酸酯的结构,重点是涉及重元素的分子结构和超分子关联。目前只知道少量铝(III)(两种)和镓(III)(一种)的结构,这些结构以及 10 种铟(III)的结构以同种结构为主,由于存在对称或几乎对称的螯合二硫代磷酸配体,大多数配位几何结构都以八面体为基础。第 13 族轻元素中的四种异质元素的分子结构各不相同,它们在晶体中的组装采用了分子间的相互作用,而不像同质结构那样涉及中心元素。铊(I)/(III)结构的情况则完全不同,其配位几何形状多种多样,通常通过 Tl⋯S 三键相互作用进行组装;在铊(I)晶体的超分子组装中,经常可以观察到 Tl(孤对)⋯π(芳基)相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A bibliographic survey of the structural chemistry of the Group 13 dithiophosphates and dithiophosphinates
A survey of the crystallographically determined structures of the Group 13 dithiophosphates and dithiophosphinates is presented with a focus upon both the molecular structures and supramolecular association involving the heavy element. Only small numbers of aluminium(III) (two) and gallium(III) (one) structures are known and these along with the 10 indium(III) examples have a preponderance towards homoleptic species with most coordination geometries based on an octahedron owing to the presence of symmetrically or almost symmetrically chelating phosphorodithiolato ligands; the notable exception is the gallium species which has an approximately tetrahedral geometry as two of the dithiophosphinate ligands coordinate in a monodentate mode. Diverse molecular structures are noted for the four heteroleptic examples of the lighter Group 13 elements which assemble in their crystals employing intermolecular interactions that do not involve the central element, as with the homoleptic structures. A completely different situation is evident for the thallium(I)/(III) structures which display a diverse array of coordination geometries and which usually assemble via Tl⋯S triel-bonding interactions; in the supramolecular assembly of thallium(I) crystals, Tl(lone-pair)⋯π(aryl) interactions are often observed.
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