The rate constants for the protonation of "free" (that is, solvated) superoxide ions by water and ethanol are equal to 0.5-3.5 X lO-~M-l.s-' in DMF and AN at 20'. It has been found that the protonation rates for the ion pairs of 0; with the BudN+ cation are much slower than those for "free" 0,. It i
Kinetics and mechanism of the reactions of the superoxide ion in solutions. I. Absorption spectra and interaction with solvents and cations
✍ Scribed by I. B. Afanas′ev; N. S. Kuprianova; N. I. Polozova
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- English
- Weight
- 486 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Absorption spectra of the superoxide ion have been studied in dimethylformamide (DMF) and acetonitrile (AN). It was found that the superoxide ion existed in equilibrium with an ion pair in AN (K~eq~ = 20__M__^−1^, Bu~4~N^+^ is the cation) and as “free” (solvated) ion in DMF. The addition of DMF caused the destruction of an ion pair in AN. The addition of the proton donors HX (water or ethanol) to the \documentclass{article}\pagestyle{empty}\begin{document}${\rm O}_{\rm 2}^{\overline {\rm .} }$\end{document} solutions in DMF and AN caused the formation of new ion pairs (Bu~4~N^+^\documentclass{article}\pagestyle{empty}\begin{document}${\rm O}_{\rm 2}^{\overline {\rm .} }$\end{document})~2~HX. The equilibrium constants of these ion pairs were determined in DMF and AN.
📜 SIMILAR VOLUMES
## Abstract The kinetics of the reaction of the superoxide ion with ethyl acetate have been studied in DMF, AN, and their mixtures. It was shown that the rate constants depend on the ethyl acetate concentration, which indicates the formation of an intermediate in this process. Equilibrium constants
## Abstract In this kinetic study of the reaction between the iodide ion and the __N__‐chlorosuccinimide, we have found that the reaction is first order in __N__‐chlorosuccinimide: namely, first order with respect to the iodide ion and first order with respect to the proton concentration. Based on
The oxidation of thiol-containing small molecules, peptides, and proteins in the presence of peroxides is of increasing biological and pharmaceutical interest. Although such reactions have been widely studied there does not appear to be a consensus in the literature as to the reaction products forme
## Abstract The kinetics of the reactions of [Pt(dipic)(H~2~O)] and [Pt(digly)(H~2~O)] (where H~2~dipic = pyridine‐2,6‐dicarboxylic acid and H~2~digly = glycylglycine) with oxalate ion were studied at 25°C in aqueous medium by UV–vis spectroscopy at __I__ = 0.1 mol dm^−3^ over an wide range of pH.
The kinetics and mechanisms of the reactions of aluminium(III) with pentane-2,4dione (Hpd), 1,1,1-trifluoro pentane-2,4-dione (Htfpd) and heptane-3,5-dione (Hhptd) have been investigated in aqueous solution at and ionic strength sodium per-Ϫ3 25ЊC 0.5 mol dm chlorate. The kinetic data are consistent