Kinetic and redox characteristics of phenoxyl radicals of eugenol and isoeugenol: A pulse radiolysis study
β Scribed by S. N. Guha; K. Indira Priyadarsini
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 90 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0538-8066
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β¦ Synopsis
The phenoxyl radicals of eugenol (EgOH) and isoeugenol (iEgOH) were generated by the specific one-electron oxidant N 3 ΠΈ using pulse radiolysis technique, and were charac- terized by their absorption spectra, decay and formation kinetics, and one-electron reduction potential (E 7 1 ) values. Reactivities of eugenol phenoxyl radical with the biologically important molecule, trolox C (analogue of vitamin E, β£-tocopheral), were determined. Reactions of OH with these phenols were studied at different pHs and suitable mechanisms for these reactions were suggested. Scavenging abilities of the phenols toward highly damaging BrΠΈ, NO 2 ΠΈ, and CCl 3 O 2 ΠΈ radicals were evaluated.
π SIMILAR VOLUMES
The transient absorption bands dm 3 9 Οͺ1 ( Ο 330, 525 nm, k Ο 5 Ο« 10 mol max f obtained on pulse radiolysis of N 2 O-saturated neutral aqueous solution of 4,4Π-thiodi-Οͺ1 s ) phenol (TDPH) are due to the reaction of TDPH with ΠΈOH radicals and are assigned to phenoxyl radical formed on fast deprotonat
The reactions of e aq Οͺ , CH 2 OHβ , (CH 3 ) 2 COHβ , O H β and N 3 β radicals with peroxo ΨΟͺ CO , 2 terpyridine complexes of Cu(II), Zn(II), and Cu(II)-Zn(II) in aqueous solution were investigated by pulse radiolysis. The primary products from the reduction and oxidation of the macrocyclic complexes