Orientational disorder and phase transitions in ammonium oxofluorovanadates, (NH4)3VOF5 and (NH4)3VO2F4.

Autor: Udovenko, Anatoly A., Pogoreltsev, Evgeny I., Marchenko, Yuri V., Laptash, Natalia M.
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Zdroj: Acta Crystallographica Section B: Structural Science, Crystal Engineering & Materials; Dec2017, Vol. 73 Issue 6, p1085-1094, 9p
Abstrakt: Single crystals of (NH4)3VOF5 and (NH4)3VO2F4 were obtained from aqueous fluoride solutions and phase transitions in these compounds were investigated using X-ray diffraction, differential scanning microcalorimetry (DSM) and vibrational spectroscopy. The room-temperature (RT) phases of these compounds belong to orthorhombic symmetry [ Immm and I222, Z = 6, for (NH4)3VOF5 and (NH4)3VO2F4, respectively] with similar unit-cell parameters and two independent vanadium atoms. Above RT [at 350 and 440 K for (NH4)3VOF5 and (NH4)3VO2F4, respectively], the compounds undergo reversible phase transitions into high-symmetry dynamically disordered elpasolite-like (, Z = 4) structures with six and 12 spatial orientations of the vanadium octahedron for (NH4)3VOF5 and (NH4)3VO2F4, respectively. The ligand atoms are distributed in a mixed (split) position of 24 e + 96 j, one of the ammonium groups is disordered on the tetrahedron 32 f site, but another one forms eight spatial orientations due to disorder of its hydrogen atoms in the 96 j position. DSM and spectroscopic data enable the phase transition from high temperature to room temperature to be connected with the transition from isotropic orientations of the octahedron to its two different dynamic states. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index
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