The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Reduction Potentials of One-Electron Couples Involving Free Radicals in Aqueous Solution
Abstract
Reduction of an electron acceptor (oxidant), A, or oxidation of an electron donor (reductant), A2−, is often achieved stepwise via one-electron processes involving the couples A/A⋅− or A⋅−/A2− (or corresponding prototropic conjugates such as A/AH⋅ or AH⋅/AH2). The intermediate A⋅−(AH⋅) is a free radical. The reduction potentials of such one-electron couples are of value in predicting the direction or feasibility, and in some instances the rate constants, of many free-radical reactions. Electrochemical methods have limited applicability in measuring these properties of frequently unstable species, but fast, kinetic spectrophotometry (especially pulse radiolysis) has widespread application in this area. Tables of ca. 1200 values of reduction potentials of ca. 700 one-electron couples in aqueous solution are presented. The majority of organic oxidants listed are quinones, nitroaryl and bipyridinium compounds. Reductants include phenols, aromatic amines, indoles and pyrimidines, thiols and phenothiazines. Inorganic couples largely involve compounds of oxygen, sulfur, nitrogen and the halogens. Proteins, enzymes and metals and their complexes are excluded.
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“There are two standard redox potentials for O2•− showing that it can act as a reducing agent E′(O2/O2•−) = 0.33 V or as an oxidizing agent E′(O2•−/H2O2) = 0.93 V [15]), Figure 4.”
From Superoxide Anion Chemistry—Its Role at the Core of the Innate Immunity (2023) · cites this paper as [15]
Citations
Cites
Electrochemical Methods: Fundamentals and Applications
Bard, A. J., & Faulkner, L. R. (1980) · Cited by 22,436
The Study of Fast Processes and Transient Species by Electron Pulse Radiolysis
Baxendale, J. H., & Busi, F. (1982) · Springer eBooks · doi:10.1007/978-94-009-7852-2 · Cited by 538
Substituent Effects in Organic Polarography
Zuman, P. (1967) · Springer eBooks · doi:10.1007/978-1-4684-8661-2 · Cited by 419
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Rice-Evans, C. A., Miller, N. J., & Paganga, G. (1996) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(95)02227-9 · Cited by 9,085
Understanding TiO 2 Photocatalysis: Mechanisms and Materials
Schneider, J., Matsuoka, M., Takeuchi, M., Zhang, J., Horiuchi, Y., Anpo, M., & Bahnemann, D. W. (2014) · Chemical Reviews · doi:10.1021/cr5001892 · Cited by 6,124
Generation and Detection of Reactive Oxygen Species in Photocatalysis
Nosaka, Y., & Nosaka, A. Y. (2017) · Chemical Reviews · doi:10.1021/acs.chemrev.7b00161 · Cited by 4,845
Schafer, F. Q., & Buettner, G. R. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(01)00480-4 · Cited by 4,587
Oxidative stress and the amyloid beta peptide in Alzheimer’s disease
Cheignon, C., Tomas, M., Bonnefont-Rousselot, D., Faller, P., Hureau, C., & Collin, F. (2018) · Redox Biology · doi:10.1016/j.redox.2017.10.014 · Cited by 2,185
Metadata
- Authors
- Wardman, P.
- Affiliations
- Mount Vernon Hospital (GB)
- Corresponding author
- Wardman, Peter
- ORCID
- Wardman, Peter
- Venue
- Journal of Physical and Chemical Reference Data
- Publisher
- AIP Publishing
- Published
- 1989-10-01
- Volume
- 18
- Issue
- 4
- Pages
- 1637-1755
- ISSN
- 0047-2689 (ISSN-L)
- 1529-7845
- OpenAlex
- W1979424160
- Cited by
- 2,123
- References
- 3
- Citations by year
- 2026: 66 · 2025: 63 · 2024: 99 · 2023: 76 · 2022: 96 · 2021: 114 · 2020: 77 · 2019: 88 · 2018: 81 · 2017: 96 · 2016: 80 · 2015: 80 · 2014: 77 · 2013: 71 · 2012: 61
- FWCI
- 19.63
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Physical and Chemical Reference Data (publishedVersion)
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Free Radicals and Antioxidants
- Physical Sciences › Environmental Science › Water Science and Technology › Advanced oxidation water treatment
- Physical Sciences › Chemistry › Physical and Theoretical Chemistry › Photochemistry and Electron Transfer Studies
- Keywords
- redox potential, free radicals, aqueous solutions, electron transfer, quinones, nitroaromatic compounds, phenols, aromatic amines, indole, pyrimidines, thiols, phenothiazines, inorganic oxidants, redox couples
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