The reaction between the radical cation derived from 2,2Ј-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) and phenols follows a kinetic law given by with stoichiometric coefficients between one and two. The rate constant is almost unrelated to the structure of the phenol, while the number o
Reaction of 2,2′-azinobis (3-ethylbenzothiazoline-6-sulfonic acid (ABTS) derived radicals with hydroperoxides. Kinetics and mechanism
✍ Scribed by C. Aliaga; E. A. Lissi
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 147 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
Tert-Butyl hydroperoxide and hydrogen peroxide readily react with the radical cation derived from 2,2Ј-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS). The reaction is inhibited by ABTS and protons, and can be interpreted in terms of a mechanism comprising a partially reversible electron transfer
ؒ followed by the self-reactions of the hydroperoxide derived radicals and reactions between them and another ABTS derived radical. A complete kinetic analysis allows an evaluation of the rate constant for reaction (1). A value of was obtained for both compounds.
Ϫ1 Ϫ1
0.2 M s The back reaction of process (1) is more relevant when tert-butyl hydroperoxide is employed.
📜 SIMILAR VOLUMES
The absolute bimolecular rate constants for the reactions of C 6 H 5 with 2-methylpropane, 2,3-dimethylbutane and 2,3,4-trimethylpentane have been measured by cavity ringdown spectrometry at temperatures between 290 and 500 K. For 2-methylpropane, additional measurements were performed with the puls