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Cited by 64Chemical Reaction MechanismsFree Radicals and AntioxidantsChemical Thermodynamics and Molecular Structure

Advertisement: Clark's Oxidation Reduction Potentials of Organic Systems

Clark, W·1960·The Journal of Physical Chemistry
DOI 10.1021/j100830a600
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ADVERTISEMENT RETURN TO ISSUEPREVArticleAdvertisement: Clark's Oxidation Reduction Potentials of Organic SystemsW ClarkCite this: J. Phys. Chem. 1960, 64, 1, 192Publication Date (Print):January 1, 1960Publication History Published online7 January 2004Published inissue 1 January 1960https://pubs.acs.org/doi/10.1021/j100830a600https://doi.org/10.1021/j100830a600research-articleACS PublicationsRequest reuse permissionsArticle Views569Altmetric-Citations48LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access options Get e-Alerts

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  • ERG has an unusually high midpoint potential for a thiol, being +0·06 V.

    “Its midpoint potential for a thiol is consequently unusually high, being +0·06 V v. −0·2 to −0·4 V for typical thiols including glutathione(4,39–41) and mycothiol(42,43), and −0·193 V for the also somewhat oxidising thiol cofactor coenzyme M, which is 2-mercaptoethanesulfonate(44).”

    From The biology of ergothioneine, an antioxidant nutraceutical (2020) · cites this paper as [40]

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Authors
Clark, W.
Corresponding author
Clark, W
Venue
The Journal of Physical Chemistry
Publisher
American Chemical Society (ACS)
Published
1960-01
Volume
64
Issue
1
Pages
192-192
ISSN
  • 0022-3654 (ISSN-L)
  • 1541-5740
DOI
10.1021/j100830a600
OpenAlex
W1963533609
Cited by
64
References
0
Citations by year
2026: 1 · 2025: 1 · 2024: 2 · 2023: 1 · 2022: 3 · 2021: 1 · 2020: 1 · 2018: 3 · 2017: 1 · 2015: 1 · 2014: 2 · 2012: 2
FWCI
2.66
Type
journal article
Language
en
Open access
closed
Locations
The Journal of Physical Chemistry (publishedVersion)
Topics
  • Physical Sciences › Chemistry › Organic Chemistry › Chemical Reaction Mechanisms
  • Physical Sciences › Chemistry › Organic Chemistry › Free Radicals and Antioxidants
  • Physical Sciences › Chemistry › Organic Chemistry › Chemical Thermodynamics and Molecular Structure
Keywords
redox potential, organic systems, organic redox chemistry

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