Formate-driven catalysis and mechanism of an iridium-copper complex for selective aerobic oxidation of aromatic olefins in water†

A hetero-dinuclear Ir-III-Cu-II complex with two adjacent sites was employed as a catalyst for the aerobic oxidation of aromatic olefins driven by formate in water. An Ir-III-H intermediate, generated through formate dehydrogenation, was revealed to activate terminal aromatic olefins to afford an Ir-alkyl species, and the process was promoted by a hydrophobic [Ir-III-H]-[substrate aromatic ring] interaction in water. The Ir-alkyl species subsequently reacted with dioxygen to yield corresponding methyl ketones and was promoted by the presence of the Cu-II moiety under acidic conditions. The Ir-III-Cu-II complex exhibited cooperative catalysis in the selective aerobic oxidation of olefins to corresponding methyl ketones, as evidenced by no reactivities observed from the corresponding mononuclear Ir-III and Cu-II complexes, as the individual components of the Ir-III-Cu-II complex. The reaction mechanism afforded by the Ir-III-Cu-II complex in the aerobic oxidation was disclosed by a combination of spectroscopic detection of reaction intermediates, kinetic analysis, and theoretical calculations.

Automated summary

The hetero-dinuclear Ir-III-Cu-II complex catalyzes the aerobic oxidation of aromatic olefins in water driven by formate, generating Ir-alkyl species and promoting the reaction with Cu-II under acidic conditions. This cooperative catalysis is revealed through spectroscopic detection, kinetic analysis, and theoretical calculations.