Synthesis and Crystal Structure of Indium Tellurium Trioxide Bromide

Synthesis and Reactivity in Inorganic Metal-Organic and Nano-Metal Chemistry (Impact Factor: 0.53). 04/2009; 39(4):209-210. DOI: 10.1080/15533170902858211


The pale yellow air-stable compound InTeO3Br could be obtained by the reaction of In, TeO2, Te and Br2. The compound crystallizes in the monoclinic crystal system (a=8.2596 (4) Å, b = 6.8752(3) Å, c = 7.1394 (3) Å, β = 103.121 (2)^, Z = 4, space group = P21/c),[1] isotypic to the corresponding chloride compound, InTeO3Cl.[2] The compound forms a layered structure and these layers are separated by van der Waal's gaps. InO4Br2 octahedra linked with the TeO3 by sharing common corners are the typical structural building blocks for the title compound.

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    ABSTRACT: Four new alkali metal indium tellurites, NaIn(TeO3)2, KIn(TeO3)2, RbInTe3O8, and CsInTe3O8, have been prepared through hydrothermal and solid state synthesis reactions using corresponding alkali metal carbonates, In2O3 [or In(NO3)3·xH2O], and TeO2. The structures of the reported materials have been determined by powder and single crystal X-ray diffraction. The mixed indium tellurites reveal a rich structural chemistry with different channel structures. NaIn(TeO3)2 shows 8-membered rings, whereas stoichiometrically similar KIn(TeO3)2 exhibits both 8- and 12-membered rings in the frameworks. Isostructural RbInTe3O8 and CsInTe3O8 reveal three-dimensional frameworks consisting of InO6, TeO3, and TeO4 groups. Close structural examination suggests that the alkali metal cation size and variable coordination modes of Te(4+) cations cooperatively influence the framework geometries of the new mixed metal tellurites. Detailed characterizations including spectroscopic, elemental, and thermal analyses are introduced. Local dipole moments and out-of-center distortions for the constituent polyhedra are also reported.
    ChemInform 10/2014; 53(20). DOI:10.1021/ic502108a