Predicting the activity of phenolic antioxidants: theoretical method, analysis of substituent effects, and application to major families of antioxidants.
By J. Wright, Erin R. Johnson, Gino Dilabio. Journal of the American Chemical Society, 2001
1,442 citations recorded by the source corpus.
Subfields: Biochemistry, Computational Theory and Mathematics, Organic Chemistry
View Paper: https://www.semanticscholar.org/paper/9fb5b416e0971b0e7f6670766907c3a9aaa7f829
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Biochemistry
- Isabel C. F. R. Ferreira
- L. Barros
- Rui M. V. Abreu
- I. Munteanu
- J. Lambert
- Constantin Apetrei
- R. Elias
In Computational Theory and Mathematics
In Organic Chemistry
Citations in the corpus
- Antioxidants in wild mushrooms. (2009, background): “To be effective ArO • must be a relatively stable free radical, so that it reacts slowly with substrate RH but rapidly with RO2 • , hence the term “chain-breaking antioxidant” [100].”
- Assessment of antioxidant capacity in vitro and in vivo. (2010, neutral): “The relative importance of the two mechanisms is dependent on the environment [23].”
- Analytical Methods Used in Determining Antioxidant Activity: A Review (2021, background): “The tests based on the transfer of a single electron, also called electron transfer (ET) tests, detect the ability of an antioxidant to transfer an electron in order to reduce metallic ions, carbonyl groups and free radicals [21].”
- Variability of the phenolic profile in the diatom Phaeodactylum tricornutum growing under copper and iron stress (2013, background): “The antioxidant activity is not only dependent on the concentration of antioxidants, but also on the structure (Wright et al. 2001).”
- The antioxidant and pro-oxidant activities of green tea polyphenols: a role in cancer prevention (2010, methodology): “4) is dependent on the bond dissociation enthalpy of the catechins, as the weaker the O-H bond of the hydroxyl group, the faster the reaction with the peroxyl radical [14].”