Cooperative Effects of Cation Size and Variable Coordination Modes of Te<sup>4+</sup> on the Frameworks of New Alkali Metal Indium Tellurites, NaIn(TeO<sub>3</sub>)<sub>2</sub>, KIn(TeO<sub>3</sub>)<sub>2</sub>, RbInTe<sub>3</sub>O<sub>8</sub>, and CsInTe<sub>3</sub>O<sub>8</sub>
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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 Te4+ 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.




