4.8 Review

Free Energies of Proton-Coupled Electron Transfer Reagents and Their Applications

期刊

CHEMICAL REVIEWS
卷 122, 期 1, 页码 1-49

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemrev.1c00521

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资金

  1. National Science Foundation Graduate Research Fellowships [F32GM1329266-02, F32GM129902]
  2. U.S. National Institutes of Health Ruth L. Kirschstein Postdoctoral Fellowships - U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [2R01GM50422]
  3. NSF [CHE-1904813]

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This paper provides an update and revision to a 2010 review on proton-coupled electron transfer (PCET) reagent thermochemistry, correcting systematic errors and presenting updated tables of thermochemical values. It discusses new conclusions and opportunities arising from the assembled data and techniques, emphasizing the importance of updated thermochemical cycles in PCET reactions for calculation and measurement of Gibbs free energies. Additionally, the paper introduces several emerging fields in PCET thermochemistry, highlighting the diversity of research being conducted in this rapidly growing field.
We present an update and revision to our 2010 review on the topic of proton-coupled electron transfer (PCET) reagent thermochemistry. Over the past decade, the data and thermochemical formalisms presented in that review have been of value to multiple fields. Concurrently, there have been advances in the thermochemical cycles and experimental methods used to measure these values. This Review (i) summarizes those advancements, (ii) corrects systematic errors in our prior review that shifted many of the absolute values in the tabulated data, (iii) provides updated tables of thermochemical values, and (iv) discusses new conclusions and opportunities from the assembled data and associated techniques. We advocate for updated thermochemical cycles that provide greater clarity and reduce experimental barriers to the calculation and measurement of Gibbs free energies for the conversion of X to XHn in PCET reactions. In particular, we demonstrate the utility and generality of reporting potentials of hydrogenation, E degrees(V vs H-2), in almost any solvent and how these values are connected to more widely reported bond dissociation free energies (BDFEs). The tabulated data demonstrate that E degrees(V vs H-2) and BDFEs are generally insensitive to the nature of the solvent and, in some cases, even to the phase (gas versus solution). This Review also presents introductions to several emerging fields in PCET thermochemistry to give readers windows into the diversity of research being performed. Some of the next frontiers in this rapidly growing field are coordination-induced bond weakening, PCET in novel solvent environments, and reactions at material interfaces.

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