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Mechanistic dichotomies in redox reactions of mononuclear metal-oxygen intermediates
- Title
- Mechanistic dichotomies in redox reactions of mononuclear metal-oxygen intermediates
- Authors
- Fukuzumi S.; Cho K.-B.; Lee Y.-M.; Hong S.; Nam W.
- Ewha Authors
- 남원우; Shunichi Fukuzumi; 이용민
- SCOPUS Author ID
- 남원우; Shunichi Fukuzumi; 이용민
- Issue Date
- 2020
- Journal Title
- Chemical Society Reviews
- ISSN
- 0306-0012
- Citation
- Chemical Society Reviews vol. 49, no. 24, pp. 8988 - 9027
- Publisher
- Royal Society of Chemistry
- Indexed
- SCIE; SCOPUS
- Document Type
- Review
- Abstract
- There are mechanistic dichotomies with regard to the formation, electronic structures and reaction mechanisms of metal-oxygen intermediates, since these metal-oxygen species could be composed of different resonance structures or canonical structures of the oxidation states of metals and ligands, which may undergo different reaction pathways. Even the same metal-oxygen intermediates, such as metal-oxo species, may undergo an electron-transfer pathway or a direct hydrogen or oxygen atom transfer pathway depending on the one-electron redox potentials of metal-oxo species and substrates. Electron-transfer pathways are also classified into two mechanisms, such as outer-sphere and inner-sphere pathways. The one-electron redox potentials of metal-oxygen species and substrates are also shifted because of the binding of acids, which can result from either hydrogen bonding or protonation. There are a rebound pathway and a non-rebound pathway following the initial electron transfer or hydrogen atom transfer step to produce hydroxylated products, depending on the one-electron redox potentials of metal-oxo species and substrates. Nucleophilic reactions can be switched to electrophilic pathways, depending on reaction conditions such as reaction temperature. Spin states of metal-oxygen intermediates are also an important factor that controls the redox reactivity of oxidants in oxidation reactions. Here, we review such various mechanistic dichotomies in redox reactions of metal-oxygen intermediates with the emphasis on understanding and controlling the redox reactivity of metal-oxygen intermediates from experimental and theoretical points of view. This journal is © The Royal Society of Chemistry.
- DOI
- 10.1039/d0cs01251c
- Appears in Collections:
- 자연과학대학 > 화학·나노과학전공 > Journal papers
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