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Crystal structure of dilead(II) oxochromate(VI) oxotellurate(IV)

机译:铅(II)铬铬酸盐(VI)氧碲酸盐(IV)的晶体结构

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摘要

Reaction of chromium(III) precursors with TeO2 in PbF2/PbO melts in air led to oxidation of chromium(III) to chromium(VI), whereas tellurium remained its oxidation state of IV. In the resulting title compound, Pb2(CrO4)(TeO3), the two types of anions are isolated from each other, hence a double salt is formed. The two independent Pb2+ cations exhibit coordination number nine under formation of very distorted coordination polyhedra [bond-length range = 2.363 (6)–3.276 (7) Å]. The oxochromate(VI) and oxotellurate(IV) anions have tetra­hedral and trigonal–pyramidal configurations, respectively. In the crystal structure, (001) layers of metal cations alternate with layers of TeO3 2− and CrO4 2− anions along [001], forming a three-dimensional framework structure. Pb2(CrO4)(TeO3) is isotypic with its sulfate analogue Pb2(SO4)(TeO3) and is comparatively discussed.
机译:在空气中PbF2 / PbO中,铬(III)前体与TeO2的反应导致空气中铬(III)氧化成铬(VI),而碲保持IV的氧化态。在所得标题化合物Pb2(CrO4)(TeO3)中,两种阴离子彼此分离,因此形成了复盐。在非常扭曲的配位多面体的形成下,两个独立的Pb 2 + 阳离子的配位数为9 [键长范围= 2.363(6)–3.276(7)]。含铬铬酸盐(VI)和含氧碲酸盐(IV)的阴离子分别具有四面体和三角锥型构型。在晶体结构中,沿着[001],(001)个金属阳离子层与TeO3 2-和CrO4 2-阴离子层交替,形成三维骨架结构。 Pb2(CrO4)(TeO3)与硫酸盐类似物Pb2(SO4)(TeO3)是同型的,并进行了比较讨论。

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