4.8 Article

Proton-Coupled Electron Transfer: Moving Together and Charging Forward

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 137, Issue 28, Pages 8860-8871

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.5b04087

Keywords

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Funding

  1. National Science Foundation [CHE-1361293]
  2. National Institutes of Health [GM056207]
  3. Center for Chemical Innovation of the National Science Foundation Solar Fuels Grant [CHE-1305124]
  4. Center for Molecular Electrocatalysis, an Energy Frontier Research Center - U.S. Department of Energy, Office of Science, Basic Energy Sciences
  5. Air Force Office of Scientific Research under AFOSR [FA9550-14-1-0295]
  6. Direct For Mathematical & Physical Scien
  7. Division Of Chemistry [1361293] Funding Source: National Science Foundation

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Proton-coupled electron transfer (PCET) is ubiquitous throughout chemistry and biology. This Perspective discusses recent advances and current challenges in the field of PCET, with an emphasis on the role of theory and computation. The fundamental theoretical concepts are summarized, at-id expressions for rate constants and kinetic isotope effects are provided. Computational methods for calculating-reduction potentials and pK(a)'s for molecular electrocatalysts, as well as insights into linear correlations and non-innocent ligands, are also described: In addition, computational methods for simulating the nonadiabatic dynamics of photoexcited PCET are discussed. Representative applications to PCET in solution, proteins, electrochemistry, and photoinduced processes are presented, highlighting the interplay between theoretical and experimental studies. The current challenges and suggested future directions are outlined for each type of application, concluding with an overall view to the future.

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