## Abstract The kinetics and mechanism of the adduct formation of diorganotin(IV)dichlorides with Co(II) tetraaza Schiff base complexes, such as [Co(ampen)] {[__N__,__N__′‐ethylenebis‐(__o__‐amino‐α‐phenylbenzylideneiminato)cobalt(II)]}, [Co(campen)] {[__N__,__N__′‐ethylenebis‐(5‐chloro‐__o__‐amino
Kinetics and mechanism of adducts formation of tetraaza cobalt(II) complexes with some organic bases in DMF solvent
✍ Scribed by Mozaffar Asadi; Zahra Asadi
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 218 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The kinetics and mechanism of the adduct formation of two Co(II) tetraaza complexes, [Co(ampen)] {[(N,N′‐ethylenebis‐(o‐amino‐α‐phenylbenzylideneiminato)cobalt(II)]} and [Co(campen)] {[(N,N′‐ethylenebis‐(5‐chloro‐o‐amino‐α‐phenylbenzylideneiminato)cobalt(II)]}, with four organic bases, 4‐nitro imidazole (4‐NO~2~Imid), 4‐methyl imidazole (4‐MeImid), imidazole (Imid), and 1‐methyl imidazole (1‐MeImid), in DMF were studied spectrophotometrically. The kinetic parameters and the second‐order k~2~ rate constants show the following nucleophilicity trend of the bases toward the given substrate: 4‐NO~2~Imid > 4‐MeImid > Imid > 1‐MeImid. The linear plots of k~obs~ vs. the molar concentration of the base, the high span of k~2~ values, and the large negative values of Δ__S__^≠^ suggest an associative (A) mechanism. © 2007 Wiley Periodicals, Inc. 39: 137–144, 2007
📜 SIMILAR VOLUMES
## Abstract The kinetics of reversible complexation of oxalatopentaammine cobalt(III) with Ni^2+^ has been investigated in MeOH + water media (0–50 (v/v) % MeOH) at 15.0–35.0°C and I = 0.10 mol dm^−3^. Analysis of rate data indicates that the monobonded complex [(NH~3~)~5~ · CoOCOCO~2~Ni]^3+^ in wh
The kinetics of base hydrolysis of some (aminomonocarboxylato)(tetraethylenepentamine)cobalt(III) complexes, [(tetren have been investigated in methanol-water media (0-80 vol % MeOH) at 15.0 Յ tЊC Յ 40.0 (0.02 mol dm Ϫ3 NaOH). The second-order rate constant at zero ionic strength, k 2 Њ, increases