Affiliation:
1. State Key Laboratory of Chemical Resource Engineering College of Chemistry Beijing University of Chemical Technology Beijing 100029 China
Abstract
AbstractLight‐driven carboxylation offers a promising approach for synthesizing valuable fine chemicals under mild conditions. Here we disclose a heterogeneous photocatalytic strategy of C(sp2)−H activation of formate for hydrocarboxylation of alkenes over zinc indium sulfide (ZnIn2S4) under visible light. This protocol functions well with a variety of substituted styrenes with good to excellent yields; it also works for unactivated alkenes albeit with lower yields. Mechanistic studies confirm the existence of CO2⋅− as a key intermediate. It was found that C(sp2)−H activation of formate is induced by S⋅ species on the surface of ZnIn2S4 via hydrogen atom transfer (HAT) instead of a photogenerated hole oxidation mechanism. Moreover, both cleavage of the C(sp2)−H of HCOO− and formation of a benzylic anion were found to be involved in the rate‐determining step for the hydrocarboxylation of styrene.
Funder
National Natural Science Foundation of China
Fundamental Research Funds for the Central Universities of Beijing University of Chemical Technology