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Investigation of the scavenging mechanism of tyrosyl radical by hydroxybenzohydroxamic acid derivatives: A DFT study.
- Source :
- Computational & Theoretical Chemistry; Aug2013, Vol. 1018, p35-44, 10p
- Publication Year :
- 2013
-
Abstract
- Highlights: [•] Kinetic data indicate that trimidox is more active radical scavenger than other investigated compounds. [•] The most favorable mechanism for studied compounds is hydrogen atom transfer (HAT). [•] The results indicate that compounds with adjacent hydroxyl group on phenyl ring are most efficient hydrogen-donor systems. [•] The computational values are in accordance with experimental findings. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 2210271X
- Volume :
- 1018
- Database :
- Supplemental Index
- Journal :
- Computational & Theoretical Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 89511577
- Full Text :
- https://doi.org/10.1016/j.comptc.2013.05.026