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

Reaction of chromium(III) precursors with TeO(2) in PbF(2)/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, Pb(2)(CrO(4))(TeO(3)), the two types of anions are isolated from each other, hence a d...

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Detalles Bibliográficos
Autor principal: Weil, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458308/
https://www.ncbi.nlm.nih.gov/pubmed/28638643
http://dx.doi.org/10.1107/S2056989017006995
Descripción
Sumario:Reaction of chromium(III) precursors with TeO(2) in PbF(2)/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, Pb(2)(CrO(4))(TeO(3)), the two types of anions are isolated from each other, hence a double salt is formed. The two independent Pb(2+) 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 TeO(3) (2−) and CrO(4) (2−) anions along [001], forming a three-dimensional framework structure. Pb(2)(CrO(4))(TeO(3)) is isotypic with its sulfate analogue Pb(2)(SO(4))(TeO(3)) and is comparatively discussed.