Selectivity among Dehydrogenation Steps for Alkyl Groups on Metal Surfaces: Comparison between Nickel and Platinum

Abstract

The thermal chemistry of ethyl and neopentyl iodides on Pt(111) surfaces was investigated by temperature-programmed desorption and reflection−absorption infrared (RAIRS) spectroscopies. The analysis using RAIRS of the isotopic composition of the ethylidyne formed from adsorption of CH3CD2I at different temperatures provided a reasonable estimate for the difference in activation energies between α- and β-hydride elimination steps from alkyl groups adsorbed on Pt(111). A study of the reactivity of neopentyl groups on the same surface using selective deuterium labeling yielded additional information on the relative rates of α- versus γ-hydride eliminations. It was determined that C−H bond-scission steps at the α and γ positions display comparable rates and that both are several orders of magnitude slower than dehydrogenation at the β carbon. A comparison is also presented here to similar chemistry on nickel substrates, where dehydrogenation reactions are usually much faster and where α-elimination dominates over the γ counterpart. The implications of these results to catalysis are discussed in the text.