Reactions of Hf +, Ta +, and W + with O 2 and CO: Metal carbide and metal oxide cation bond energies

Abstract

The reactions of Hf +, Ta +, and W + with O 2 and CO are studied as a function of translational energy in a guided ion beam tandem mass spectrometer. All three reactions with O 2 form diatomic metal oxide cations in exothermic reactions that occur at the collision rate. In the CO systems, formation of both diatomic metal oxide and metal carbide cations is observed to be endothermic. The energy-dependent cross sections in the latter systems are interpreted to give 0 K bond energies (in eV) of D 0(HfC +) = 3.19 ± 0.03, D 0(TaC +) = 3.79 ± 0.04, D 0(WC +) = 4.76 ± 0.09, D 0(HfO +) = 6.91 ± 0.11, D 0(TaO +) = 7.10 ± 0.12, and D 0(WO +) = 6.77 ± 0.07. The present experimental values for TaO + and WC + agree well with literature thermochemistry, those for HfO + and WO + refine the available literature bond energies, and those for HfC + and TaC + are the first measurements available. The nature of the bonding in MO + and MC + is discussed and compared for these three metal ions and analyzed using theoretical calculations at a B3LYP/HW+/6-311+G(3df) level of theory. Bond energies for all MO + and MC + species are calculated using geometries calculated at this level and single point energies determined at B3LYP, CCSD, CCSD(T), QCISD, and QCISD(T) levels of theory with the same basis set. Reasonable agreement between the theoretical and experimental bond energies for the three metal oxide and three metal carbide cations is found. Potential energy surfaces for reaction of the metal cations with CO are also calculated at the B3LYP level of theory and reveal additional information about the reaction mechanisms.