The synthesis,vibrational spectra,and molecular structure of [Ir(CO)(6)][SbF(6)](3).4HF - the first structurally characterized salt with a tripositive,homoleptic metal carbonyl cation and the first example of a tetrahedral hydrogen-bonded (HF)(4) cluster

The reductive carbonylation of IrF(6) in a dilute solution of SbF(5) in anhydrous HF (1:6 by volume) produces surprisingly at 25 degrees C and 1.5 atm CO the complex salt Ir(CO)(6)]SbF(6)](3).4HF, while Ir(CO)(6)]Sb(2)F(11)](3) is obtained in liquid SbF(5) under similar conditions. Vibrational spectra in the CO stretching range for both salts and Ir(CO)(6)](3+)((solv)) are identical within error limits, and nu(CO)(av) is with 2269 cm(-1) the highest average stretching frequency so far observed for octahedral metal carbonyl cations. A vibrational assignment supported by DFT calculations is presented, and the vibrational fundamentals are compared to those of Os(CO)(6)](2+). The molecular structure of Ir(CO)(6)]SbF(6)](3).4HF is determined by single-crystal X-ray diffraction. Crystal data for Ir(CO)(6)]SbF(6)](3).4HF: rhombohedral, R3c (No. 161), a = 14.630(4) A, c = 18.377(7) A, V = 3406.4(18) A(3), Z = 6, T = 150 K, R(1) = 0.0338 I > 2sigma (I)], wR(2) = 0.0797). The average Ir-C bond length in the octahedral Ir(CO)(6)](3+) cation is with 2.029(10) the longest observed for iridium carbonyl derivatives, consistent with the absence of Ir --> CO pi-back-bonding. The four solvate HF molecules form a tetrahedron via long, asymmetric, and partly delocalized hydrogen bonds with F-F edge lengths of 2.857 (3x) and 2.914 (3x) A. There is no precedent for a polyhedral (HF)(n) cluster in the gas, liquid, or solid phase. The four F atoms of the (HF)(4) cluster are coordinated to the C atoms of the six CO ligands of the cation, which again is without precedent. The coordination of one of the F atoms to three C atoms in a iso-tridentate mode with contact distances C-F(8) of 2.641(10) A is most unusual. The observed tight C-F coordination in Ir(CO)(6)]SbF(6)](3).4HF provides conclusive evidence for the presence of electrophilic carbon in the cation and illustrates how superelectrophilic cations such as Ir(CO)(6)](3+) are solvent stabilized in the conjugate Br?nsted-Lewis superacid HF-SbF(5).