Deoxygenation of Phosphine Oxides by P^III/P^V=O Redox Catalysis via Successive Isodesmic Reactions

Deoxygenation of phosphine oxides is of great significance to synthesis of phosphorus ligands and relevant catalysts, as well as to the sustainability of phosphorus chemistry. However, the thermodynamic inertness of P=O bonds poses a severe challenge to their reduction. Previous approaches in this regard rely primarily on a type of P=O bond activation with either Lewis/Bronsted acids or stoichiometric halogenating reagents under harsh conditions. Here, we wish to report a novel catalytic strategy for facile and efficient deoxygenation of phosphine oxides via successive isodesmic reactions, whose thermodynamic driving force for breaking the strong P=O bond was compensated by a synchronous formation of another P=O bond. The reaction was enabled by P-III/P=O redox sequences with the cyclic organophosphorus catalyst and terminal reductant PhSiH3. This catalytic reaction avoids the use of the stoichiometric activator as in other cases and features a broad substrate scope, excellent reactivities, and mild reaction conditions. Preliminary thermodynamic and mechanistic investigations disclosed a dual synergistic role of the catalyst.