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Crystallographic analysis and features of cation coordination in a series of structures of sulfides with Tl+

机译:一系列具有Tl +的硫化物的晶体学分析和阳离子配位特征

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摘要

A crystallographic analysis of ellisite Tl3AsS3, fangite Tl3AsS4, lorandite TlAsS2, and synthetic Tl3AsS3 shows that the configuration of atomic positions in these structures is determined mostly by the ordering of S2- anions and the large massive Tl+ cations in a single packing. The standard coordination of the As cation is provided only by the strong covalent As-S bonds; the environment of Tl+ cations varies depending on the geometry of their packing with sulfur.
机译:对方铅矿Tl3AsS3,方铁矿Tl3AsS4,菱锰矿TlAsS2和合成Tl3AsS3的晶体学分析表明,这些结构中原子位置的构型主要由S2-阴离子和大体积Tl +阳离子在单个填料中的排列决定。 As阳离子的标准配位仅由牢固的共价As-S键提供; Tl +阳离子的环境取决于其与硫的堆积几何形状。

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