X-ray crystal structures of [XeF][MF6] (M = As, Sb, Bi), [XeF][M2F11](M = Sb, Bi) and estimated thermochemical data and predicted stabilities for noble-Gas fluorocation salts using volume-based thermodynamics

The crystal structures of the xenon(II) salts, [XeF][SbF6], [XeF[BiF6], and [XeF[Bi2F11], have been determined for the first time, and those of XeF2, [XeF][AsF6], [XeF][Sb2F11], and [XeF3][Sb2F11] have been redetermined with greater precision at -173 degrees C. The Bi2F11- anion, which has a structure analogous to those of the As2F11- and Sb2F11- anions, has been structurally characterized by single crystal X-ray diffraction for the first time as its XeF+ The fluorine bridge between the bismuth atoms is asymmetric with Bi center dot center dot center dot Fb bond lengths of 2.092(6) and 2.195(6) angstrom and a Bi center dot center dot center dot Fb'center dot center dot center dot Bi bridge bond angle of 145.3(3)degrees. The XeF+ cations interact with their anions by means of Xe center dot center dot center dot Fb center dot center dot center dot M bridges. Consequently, the solid-state Raman spectra of [XeF][MF6] (M = As, Sb, Bi) were modeled as the gas-phase ion pairs and assigned with the aid of quantum-chemical calculations. Relationships among the terminal Xe-F-1 and bridge Xe center dot center dot center dot F-b bond lengths and stretching frequencies and the gas-phase fluoride ion affinities of the parent Lewis acid that the anion is derived from are considered. The analogous krypton ion pairs, [KrF][MF6] (M = As, Sb, Bi) were also calculated and compared with their previously published X-ray crystal structures. The calculated cation-anion charge separations indicate that the [XeF][MF6] salts are more ionic than their krypton analogues and that XeF2 is a stronger fluoride ion donor than KrF2. The lattice energies, standard enthalpies, and free energies of formation for salts containing the NgF(+), Ng(2)F(3)(+), XeF3+, XeF5+, Xe2F11+, and XeOF3+ (Ng = Ar, Kr, Xe) cations were estimated using volume-based thermodynamics (VBT) based on crystallographic and estimated ion volumes. These estimated parameters were then used to predict the stabilities of noble-gas salts. VBT is used to examine and predict the stabilities of, inter alia, the salts [XeFm[SbnF5n+1] and [XeFm][AsnF5n+1] (m = 1, 3; n = 1, 2). VBT also confirms that XeF+ salts are stable toward redox decomposition to Ng, F-2, and MF5 (M = As, Sb), whereas the isolable krypton compounds and the unknown ArF+ salts are predicted to be unstable by VBT with the ArF+ salts being the least stable