OSSO]-Type Iron(III) Complexes for the Low-Pressure Reaction of Carbon Dioxide with Epoxides: Catalytic Activity, Reaction Kinetics, and Computational Study

Abstract

The selective conversion of variously substituted epoxides into the corresponding cyclic carbonates under mild reaction conditions was achieved with mononuclear Fe(III) complexes bearing bis-thioether-diphenolate [OSSO]-type ligands, in combination with tetrabutylammonium bromide (TBAB). For example, propylene carbonate was obtained in 1 h at 35 °C (turnover frequency, TOF = 290 h–1), from propylene oxide and 1 bar of CO2 pressure, using 0.1 mol % of the Fe(III) complex and 0.5 mol % of TBAB. Product divergence is observed only for cyclohexene oxide toward the exclusive formation of the aliphatic polycarbonate (TOF = 165 h–1 at 80 °C and 1 bar of CO2 pressure, using 0.1 mol % of the Fe(III) complex and 0.1 mol % of tetrabutylammonium chloride). Kinetic investigations indicated reaction orders of two and one, with respect to the Fe(III) complex, for the production of propylene carbonate and the poly(cyclohexene carbonate), respectively. The enthalpy and entropy of activation were determined using the Eyrin...