## Abstract The kinetics of replacement of H~2~O by [Ru(NH~3~)pz]^2+^ (pz = pyrazine) in [Fe(CN)~5~H~2~O]^3−^ have been studied in various concentrated electrolyte solutions and in various water–cosolvent mixtures, at 298 K. Salt and cosolvent effects can be rationalized taking into account specifi
Salt effects upon the S2O82− + Ru(NH3)5pz2+ electron transfer reaction
✍ Scribed by A. Rodríguez; P. López-cornejo; P. Pérez; F. Muriel; F. Sánchez; John Burgess
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 132 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
✦ Synopsis
A study of the kinetic salt effects on the oxidation of Ru(NH 3 ) 5 pz 2ϩ (Pirazinepentaammineruthenium (II)) with (Peroxodisulphate) was carried out. The components of 2Ϫ S O 2 8
the experimental rate constant, k obs , were separated, and the true (unimolecular) electron transfer rate constant, k et , is (approximately) obtained. An analysis of the main parameters controlling the variations of k et , the free energies of reaction and reorganization, is made. Both parameters show a compensating behavior, so there are small variations of k et and k obs when salt concentrations change.
📜 SIMILAR VOLUMES
## Abstract The kinetics of electron transfer reactions between [Fe(CN)~6~]^4−^ and [Co(NH~3~)~5~pz]^3+^ and between [Ru(NH~3~)~5~pz]^2+^ and [Co(C~2~O~4~)~3~]^3−^ was studied in concentrated salt solutions (Na~2~SO~4~, LiNO~3~, and Ca(NO~3~)~2~). An analysis of the experimental kinetic data, __k__
## Abstract The kinetics of substitution of H~2~O by Ru(NH~3~)~5~pz^2+^ (pz = pyrazine) in Fe(CN)~5~H~2~O^3−^ have been studied in micellar aqueous solutions of sodium dodecylsulfate (SDS). Experimental results are discussed by using an approach based on the transition‐state theory. This approach i
## Abstract The title reaction was studied in different water–cosolvent (methanol) mixtures. The results have been rationalized employing the Marcus–Hush treatment. To apply this treatment, the true, unimolecular, electron‐transfer rate constants (__k__~et~) were obtained from the experimentally me
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
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