Solid-state motion of OTeF5− compounds: detection by 19F NMR and IR spectroscopy and correlation with the X-ray structure of an orthorhombic crystalline modification of [C14H19N2+][OTeF5−] (C14H19N2+ = protonated 1,8-bis(dimethylamino)naphthalene)

Abstract

An orthorhombic crystalline modification of [(PS)H⁺][OTeF₅⁻] was studied by single crystal X-ray diffraction ((PS)H⁺ = protonated 1,8-bis(dimethylamino)naphthalene): orthorhombic, space group Cmcm, a = 8.607(2), b = 14.048(3), c = 13.365(2) Å, Z = 4, T = −130 °C. The structural parameters for the anion and cation in this modification (Mod-B) are very similar to those for the previously reported triclinic modification of this salt (Mod-A). However, variable temperature IR spectra for Mod-B suggest that the OTeF₅⁻ anion is exhibiting a two-site O/F_ax interchange above −70 °C. Solid-state ¹⁹F NMR spectra suggest that this interchange may be as rapid as 10⁴–10⁵ s⁻¹ at room temperature. Keywords: crystal structure of protonated 1,8-bis(dimethylamino)naphthalene)pentafluorotellurate(VI), polymorphism, solid state ¹⁹FNMR.