The ligand substitution reaction Fe(CN) 5 H 2 O 3Ϫ ϩ pyrazine : Fe(CN) 5 pyrazine 3Ϫ ϩ H 2 O has been studied in sodium dodecyl sulfate, SDS, hexadecyltrimethylammonium bromide, CTAB, and salt aqueous solutions at 298.2 K. Kinetics were studied in dilute and concentrated salt solutions and in SDS an
Study of the reaction Fe(CN)5(4-CNpy)3− + S2O82− in aqueous salt and micellar solutions
✍ Scribed by Gaspar Fernández; María Del Mar Graciani; Amalia Rodríguez; María Múñoz; María Luisa Moyá
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 149 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
The reaction (4-CNpy ϭ 4-cyanopyridine) was studied 3Ϫ 2Ϫ Fe(CN) (4-CNpy) ϩ S O 5 2 8
in aqueous salt solutions in the presence of several electrolytes as well as in anionic, cationic, and nonionic surfactant solutions. In aqueous salt solutions the noncoulombic interactions seem to be important in determining the positive salt effects observed. The salting effects are influencing the activity coefficients of any participant in the reaction, including those ion pairs which can be formed between the anionic reagents and the cations which come from the added salts. The changes in surfactant concentration in anionic and nonionic surfactant solutions do not affect the reaction rate, which is similar to that in pure water at the same ionic strength. In cationic micellar solutions an increase in the rate constant compared to that in pure water is found; the reaction rate decreasing when the surfactant concentration increases.
The kinetic trends can be explained assuming that the reagents are totally bound to the micelles and, therefore, an increase in the surfactant concentration results in a decrease in the reagent concentrations at the micellar phase and thus in a decrease in the observed rate constant.
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Based on an activation model, a available scheme to calculate the rate of the electron-transfer reaction between transition-metal complexes in aqueous solution is presented. Ab initio technique is used to determine the electron-transfer reactivity of the type M(H 2 O) 2+/3+ 6 of transition-metal com