## Abstract The first row transition metal ions Mn^2+^, Co^2+^, and Ni^2+^ have been studied by classical umbrella sampling molecular dynamics simulations. The water exchange mechanisms, estimates of reaction rates, as well as structural changes during the activation process are discussed. Mn^2+^ w
The kinetics of complexation of nickel(II) and cobalt(II) with cinchomeronate in aqueous solution
β Scribed by Sock Sung Yun; Ki Young Choi
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 419 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0538-8066
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β¦ Synopsis
The pressure-jump method has been used to determine the rate constants for the formation and dissociation of nickel(I1) and cobalt(I1) complexes with cinchomeronate in aqueous solution at zero ionic strength. The forward and reverse rate constants obtained are k, = 2.27 x lo6 M-' s-' and k, = 3.81 x 10' s-' for the nickel(I1) complex and k , = 1.23 x lo7 M-' s-' and k, = 2.66 x 1 0 ' s-' for the cobalt(I1)) complex a t 25Β°C.
The activation parameters of the reactions have also been obtained from the temperature variation study. The results indicate that the rate determining step of the reaction is a loss of a water molecule from the inner coordination sphere of the cation for the nickel(I1) complex and the chelate ring closure for the cobalt(I1) complex. The influence of the pyridine ring nitrogen atom of the cinchomeronate ligand on the complexation of cobalt(I1) ion is also discussed.
π SIMILAR VOLUMES
The kinetics of complexation of nickel(II) with some penicillins and related compounds show that the zwitterionic form of the ligand has very low reactivity compared to the anionic form. The resolved rate constants are interpreted in terms of binding to the ring nitrogen and carboxyl group and not t
## Abstract Kinetics of reduction of the surfactant complex ions, __cis__βchloro/bromo (dodecylamine)bis(ethylenediamine)cobalt(III) by iron(II) in aqueous solution was studied at 303, 308, and 313 K by spectrophotometry method under pseudoβfirstβorder conditions, using an excess of the reductant.