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Marcus Theory: Thermodynamics CAN Control the Kinetics of Electron Transfer Reactions

2012/07/11 by Todd P. Silverstein · 18 citations
Chemistry · Engineering · Physics and Astronomy · #Electrochemical Analysis and Applications #Molecular Junctions and Nanostructures #Spectroscopy and Quantum Chemical Studies

paper · doi:10.1021/ed1007712

Abstract

Although it is generally true that thermodynamics do not influence kinetics, this is NOT the case for electron transfer reactions in solution. Marcus Theory explains why this is so, using straightforward physical chemical principles such as transition state theory, Arrhenius’ Law, and the Franck-Condon Principle. Here the background and applications of Marcus Theory are presented, with special emphasis given to biological redox reactions. Interesting conclusions that arise from the theory are also discussed. These include the nonlinear contribution of reorganization energy (λ) to the activation free energy (ΔG⧧), as well as the existence of a defined “normal range” of reaction cell potential (ΔE°): Only if ΔE° is within this range does a reaction of lower λ have a lower ΔG⧧; outside of this range, the lower-λ reaction will have the higher ΔG⧧.

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