4.8 Article

Using combinations of oxidants and bases as PCET reactants: thermochemical and practical considerations

Journal

ENERGY & ENVIRONMENTAL SCIENCE
Volume 5, Issue 7, Pages 7771-7780

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2ee03300c

Keywords

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Funding

  1. U.S. National Science Foundation Center for Enabling New Technologies through Catalysis
  2. Camille and Henry Dreyfus Postdoctoral Program in Environmental Chemistry
  3. U.S. National Institutes of Health [GM-50422]
  4. Center for Molecular Electrocatalysis
  5. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences
  6. Energy Frontier Research Center

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Studies in proton-coupled electron transfer (PCET) often require the combination of an outer-sphere oxidant and a base, to remove an electron and a proton. A common problem is the incompatibility of the oxidant and the base, because the former is electron deficient and the latter electron rich. We have tested a variety of reagents and report a number of oxidant/base combinations that are compatible and therefore potentially useful as PCET reagents. A formal bond dissociation free energy (BDFE) for a reagent combination is defined by the redox potential of the oxidant and pK(a) of the base. This is a formal BDFE because no X-H bond is homolytically cleaved, but it is a very useful way to categorize the H-center dot accepting ability of an oxidant/base PCET pair. Formal BDFEs of stable oxidant/base combinations range from 71 to at least 98 kcal mol(-1). Effects of solvent, concentration, temperature, and counterions on the stability of the oxidant/base combinations are discussed. Extensions to catalysis and related reductant/acid combinations are mentioned.

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