The remarkable nucleophilicity of superoxide anion radical. rate constants for reaction of superoxide ion with aliphatic bromides.
✍ Scribed by Wayne C. Danen; R.Jay Warner
- Publisher
- Elsevier Science
- Year
- 1977
- Tongue
- French
- Weight
- 250 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
We wish to report rate constants for the reaction of superoxide anion radical, 02', with various aliphatic bromides in dimethylsulfoxide (DMSO) solution. The results suggest that 02; is one of the most potent nucleophiles yet studied.
Superoxide ion is the radical anion derived by adding an electron to molecular oxygen and is suspected of having a widespread, albeit transitory, existence in nature. The elegant
📜 SIMILAR VOLUMES
## Abstract The decay of photochemically generated __tert__‐butyl radicals is studied at 48°C in 11 __m__‐ and __p__‐substituted toluenes by time‐resolved electron spin resonance spectroscopy. It is governed by the second‐order self‐termination perturbed by a pseudo‐first‐order reaction of the radi
## Abstract Rate constants for the gas‐phase reactions of hydroxyl radicals and chlorine atoms with a series of alcohols have been determined by using the relative method. The experiments were performed at 295 ± 2 K and at 1 atmospheric pressure. The obtained values of the rate constants in units o
## Abstract Rate constants for the gas‐phase reactions of hydroxyl radicals and chlorine atoms with aliphatic alcohols and ethers have been determined at 298 ± 2 K and at a total pressure of 1 atmosphere. The OH radical rate data were obtained using both the absolute technique of pulse radiolysis c