Catalyst Screening through Quantum Chemical Calculations and Microkinetic Modeling: Hydrolysis of Carbon Dioxide

Abstract

Quantum chemical calculations are emerging as an effective way to screen catalysts for particular applications. In this contribution, we demonstrate the power of density functional theory to study CO₂ hydrolysisby six carbonic anhydrase mimics, evaluating thermodynamic and kinetic parameters at the mechanistic level. A microkinetic model was then built based on the kinetics and thermodynamics calculated from first principles. The intrinsic reaction rate constant was calculated from the results of the microkinetic model and compared with experimental data. Overall, the rate constants were in good agreement with experimental values, except for zinc-tri and complex b, which were overestimated. This was ascribed to their ineffective complexation with Zn²⁺. How the reaction rate constants vary with time was also investigated. From 0 to 12 ms, the rate constants of complexes a and d decreased to 50 and 67% of their initial values, respectively; the rate constants of complexes b and f2 were almost invariant with time; the rate constant of complex f1 showed an unusual double sigmoidal shape. The pK_a values of these six carbonic anhydrase mimics as well as three additional mimics were calculated. A correlation between pK_a values and the binding free energy of OH-was obtained by fitting data from five zinc(II) aza-macrocyclic complexes. The reaction rate constants were found to increase linearly with the pK_a value, indicating CO₂ adsorption is the rate-limiting step.