Oxidation of N-(2-hydroxyethyl)ethylenediamine triacetate Oxidation of N-(2-hydroxyethyl)ethylenediamine triacetate tris(polypyridy)iron(III) complexes and the tate(III) ion
Oxidation of ethylenediaminetetraacetate bytris(diimine) iron(III) complexes and the dodecatungstocobaltate(III) ion: a comparative kinetic and mechanistic study
β Scribed by Godwin A. Ayoko; Jemi F. Iyun; Saratu Mamman
- Publisher
- Springer
- Year
- 1994
- Tongue
- English
- Weight
- 279 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0340-4285
No coin nor oath required. For personal study only.
β¦ Synopsis
The stoichiometry and kinetics of the oxidation of ethylenediaminetetraacetate by [Fe(phen)3] 3 +, [Fe(bipy)3] 3 + and [ComW12040] 5-were studied in aqueous HC10 a. Reaction rates were first order with respect to the oxidants and the reductant, and the dependence of the second order rate constant k2 on [H + ] is given by k2 = a + b[H+] -1.
The primary products were CO2, CH20 and (CHzNH2) 2. Schuster treatment is employed to show that the reactions occur by the outersphere mechanism.
π SIMILAR VOLUMES
The kinetics of oxidation of cyclohexanone(chxn), a-butanone(but), and 1,3-dihydroxy-2-propanone (dhp) have been investigated in aqueous acidic media. A first-order dependence in complex is obtained at high acid and low oxidant concentration for these ketones. However, a zero-order rate prevails at
## Abstract The oxidation of __trans__βstilbene, phenylacetylene, and diphenylacetylene by Tl(OAc)~3~ in aqueous acetic acid medium in the presence of HClO~4~ follows the rate law in [H^+^] of 0.1β1.0__M__, the [H^+^] dependence below 0.1__M__ being marginal. The reactions are strongly dielectric
The oxidation of dl-ornithine monohydrochloride (OMH) by diperiodatocuprate(III) (DPC) has been investigated both in the absence and presence of ruthenium(III) catalyst in aqueous alkaline medium at a constant ionic strength of 0.20 mol dm -3 spectrophotometrically. The stiochiometry was same in bot