Abstract
Density functional theory (DFT) calculations were used to study the mechanisms for hydrogenation of biomass-derived levulinic acid (LA) to γ-valerolactone (GVL) catalyzed by PNP-ligated (PNP = 2,6-bis(di-ter-butylphosphinomethyl) pyridine) iridium complexes, (tBuPNP)IrH3, 1. The transformation proceeds dearomatization/rearomatization including four stages: hydride transfer to give LA-H− and dihydride iridium specie (BtuPNP)IrH2+, methylene proton in the PNP ligand transfer to substrate to form γ-hydroxyvaleric acid (HVA), catalyst regeneration via H2 splitting, cyclization of HVA to GVL. Compared with the hydrogenation of CO2 catalyzed by the same complex, herein the rate-limiting step is the hydride transfer step rather than the methylene proton transfer. The calculations show that the hydride transfer step has a significantly higher barrier (21.1 vs 5.3 kcal mol−1 for the hydrogenation of CO2). Besides, the cyclization is very easily achieved due to the low barrier. As an alternative pathway, different from the above dearomatization/rearomatization process, a base abstracts a proton from the dihydrogen ligand to form the trihydride iridium with a free energy barrier of 24.6 kcal mol−1. Our results will help in the understanding of the mechanisms of hydrogenation of LA to GVL catalyzed by metal complexes.
Published Version
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