Preparation of XeOF<sub>3</sub><sup>+</sup>·Sb<sub>2</sub>F<sub>11</sub><sup>–</sup>and XeO<sub>2</sub>F<sup>+</sup>·Sb<sub>2</sub>F<sub>11</sub><sup>–</sup>.<sup>19</sup>F nuclear magnetic resonance and Raman spectra of XeOF<sub>3</sub><sup>+</sup>and XeO<sub>2</sub>F<sup>+</sup>

R. J. Gillespie, B. Landa, G.J. Schrobilgen

Journal of the Chemical Society Chemical Communications · 1972 · 13 citations · 0 references

Concepts

Abstract

The 19F n.m.r. spectra of solutions in SbF5 and the Raman spectra of the solids show that the compounds XeOF4·2SbF5 and XeO2F2·2SbF5 have the ionic structures XeOF3+·Sb2F11– and XeO2F+·Sb2F11–, that the XeOF3+ ion has the expected trigonal bipyramidal AX4E type structure and that the XeO2F+ ion has a pyramidal structure analogous to the isoelectronic XeO3.