The kinetics and mechanism of the reaction of complexation of iron(II1) with 2,4-octanedione and 2,4-nonanedione have been investigated spectrophotometrically in aqueous solution at 10°C and ionic strength 0.5 mol dm-3 NaC104. The equilibrium constants of the monocomplexes have been determined. The
Mono-complex formation kinetics of 2-acetylcyclohexanonatochromium(III) in aqueous solution
✍ Scribed by Carlos A. Blanco; José M. Hernando; Manuel Mateo
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 451 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
The kinetics and mechanism of the reaction of complexation of chromium(II1) with 2-acetylcyclohexanone has been investigated spectrophotometrically in aqueous solution at 50°C and ionic strength 0.5 mol dm-3 NaC104. The equilibrium constants of the complex have been determined. The mechanism proposed to account for the kinetic data involves a double reversible pathway where both Cr3' and Cr(OH)" react with the enol tautomer of the ligand with rate constants of 9.6 X dm3 mol-' s-l, respectively. Some discussions are made on the basis of Eigen-Wilkins theory considering the effect of solvent exchange on the complex formation. dm3 mol-' s-', and 3.69 X
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## Abstract The results of comprehensive equilibrium and kinetic studies of the iron(III)–sulfate system in aqueous solutions at I = 1.0 M (NaClO~4~), in the concentration ranges of __T__ = 0.15–0.3 mM, and at pH 0.7–2.5 are presented. The iron(III)–containing species detected are FeOH^2+^ (=FeH~−1