Proton-coupled electron transfer (PCET) reactions play a vital role in a wide range of chemical and biological processes. Recent advances in the theory of PCET will be presented. The quantum mechanical effects of the active electrons and transferring proton, as well as the motions of the proton donor-acceptor mode and solvent or protein environment, are included in a general theoretical formulation. This formulation enables the calculation of rate constants and kinetic isotope effects for comparison to experiment. Applications to PCET reactions in solution, enzymes, and electrochemical systems will be presented. Studies of the enzyme soybean lipoxygenase provide a physical explanation for the experimental observation of unusually high kinetic isotope effects for C-H bond activation at room temperature. Investigations of molecular electrocatalysts for hydrogen production identify the thermodynamically and kinetically favorable mechanisms and guide the theoretical design of more effective molecular electrocatalysts. In addition, recent developments of theoretical approaches for simulating the ultrafast dynamics of photoinduced PCET will be discussed. These calculations provide insights into the roles of proton vibrational relaxation and nonequilibrium solvent dynamics in photoinduced PCET processes.

Proton-coupled electron transfer in catalysis and energy conversion

251st National Meeting (2016)

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