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Deuterium kinetic isotope effects as redox mechanistic criterions
This account article focuses on deuterium kinetic isotope effects (KIEs) used as criterions to elucidate redox mechanisms including proton‐, hydrogen‐ and hydride‐transfer reactions. Hydrogen atom transfer (HAT) is composed of two elementary steps: electron transfer (ET) and proton transfer (PT), wh...
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Published in: | Bulletin of the Korean Chemical Society 2021, 42(12), , pp.1558-1568 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | This account article focuses on deuterium kinetic isotope effects (KIEs) used as criterions to elucidate redox mechanisms including proton‐, hydrogen‐ and hydride‐transfer reactions. Hydrogen atom transfer (HAT) is composed of two elementary steps: electron transfer (ET) and proton transfer (PT), while hydride transfer is composed of three elementary steps: ET, PT, and ET. Large tunneling effects are often observed for proton‐coupled electron‐transfer (PCET) reactions of metal–oxygen complexes in which ET occurs to the metal center and PT occurs simultaneously to the ligand, exhibiting large KIEs. Whether HAT proceeds via sequential ET/PT, PT/ET, or concerted PCET (cPCET) depending on the redox properties of hydrogen donors and acceptors to exhibit different KIEs. Whether hydride transfer also proceeds via sequential ET/PT/ET, PT/ET/ET, or cPCET/ET depending on the redox properties of hydride donors and acceptors to exhibit different KIEs. Temperature dependence of KIEs for aldehyde deformylation reactions has enabled to distinguish two reaction pathways: one is a HAT and the other is a nucleophilic addition. The change of the mechanism from cPCET to sequential ET/PT is made possible by binding acids to the hydrogen and hydride acceptors when no KIE is observed. Inverse KIEs are also discussed for acid (or deuteron)‐promoted ET reactions.
This account article focuses on deuterium kinetic isotope effects (KIEs) used as criterions to elucidate redox mechanisms. KIEs are shown to be used to distinguish redox mechanisms such as electron transfer, proton transfer, and hydrogen atom transfer. Inverse KIEs can also be obtained in the acid‐promoted electron‐transfer reactions. Thus, KIE and inverse KIE provide valuable insights into the redox mechanisms. |
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ISSN: | 1229-5949 0253-2964 1229-5949 |
DOI: | 10.1002/bkcs.12417 |