Acta Crystallographica Section E: Crystallographic Communications (May 2018)

Syntheses, Raman spectroscopy and crystal structures of alkali hexafluoridorhenates(IV) revisited

  • James Louis-Jean,
  • Samundeeswari Mariappan Balasekaran,
  • Dean Smith,
  • Ashkan Salamat,
  • Chien Thang Pham,
  • Frederic Poineau

DOI
https://doi.org/10.1107/S2056989018005297
Journal volume & issue
Vol. 74, no. 5
pp. 646 – 649

Abstract

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The A2[ReF6] (A = K, Rb and Cs) salts are isotypic and crystallize in the trigonal space group type P\overline{3}m1, adopting the K2[GeF6] structure type. Common to all A2[ReF6] structures are slightly distorted octahedral [ReF6]2− anions with an average Re—F bond length of 1.951 (8) Å. In those salts, symmetry lowering on the local [ReF6]2− anions from Oh (free anion) to D3d (solid-state structure) occur. The distortions of the [ReF6]2− anions, as observed in their Raman spectra, are correlated to the size of the counter-cations.

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