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We describe herein the novel application of a transition metal oxo complex, a cationic oxorhenium(V) oxazoline, in the production of molecular hydrogen (H2) from the catalytic hydrolytic oxidation of organosilanes. The main highlights of the reaction are quantitative hydrogen yields, low catalyst loading, ambient conditions, high selectivity for silanols, water as the only co-reagent, and no solvent requirement. The amount of hydrogen produced is proportional to the water stoichiometry. Thus, reaction mixtures of polysilyl organics such as HC(SiH3)3 and water contain potentially >6 wt % hydrogen. Kinetic and isotope labeling experiments have revealed a new mechanistic paradigm for the activation of Si-H bonds by oxometalates.
Ison et al. (Mon,) studied this question.