Probing adsorption of methane onto vanadium cluster cations via vibrational spectroscopy.

Abstract

Photofragment spectroscopy is used to measure the vibrational spectra of V2+(CH4)n (n = 1-4), V3+(CH4)n (n = 1-3), and Vx+(CH4) (x = 4-8) in the C-H stretching region (2550-3100 cm-1). Spectra are measured by monitoring loss of CH4. The experimental spectra are compared to simulations at the B3LYP+D3/6-311++G(3df,3pd) level of theory to identify the geometry of the ions. Multi-reference configuration interaction with Davidson correction (MRCI+Q) calculations are also carried out on V2+ and V3+. The methane binding orientation in V2+(CH4)n (n = 1-4) evolves from η3 to η2 as more methane molecules are added. The IR spectra of metal-methane clusters can give information on the structure of metal clusters that may otherwise be hard to obtain from isolated clusters. For example, the V3+(CH4)n (n = 1-3) experimental spectra show an additional peak as the second and third methane molecules are added to V3+, which indicates that the metal atoms are not equivalent. The Vx+(CH4) show a larger red shift in the symmetric C-H stretch for larger clusters with x = 5-8 than for the small clusters with x = 2, 3, indicating increased covalency in the interaction of larger vanadium clusters with methane.