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
Effect of solvent on the reactions of coordination complexes: Part 15: Base hydrolysis ofCis-(Chloro)(benzimidazole)-Bis-(ethylenediamine)cobalt(III) ion in mixed solvent media
✍ Scribed by Anadi C. Dash; Neelamadhab Dash
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 390 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
The kinetics of base hydrolysis of the cis-(chloro)-(benzimidazole)bis(ethylenediamine) cobalt(II1) ion was investigated in Methanol-water and Ethyleneglycol-water media of varying compositions and at isodielectric conditions (Ds = 61 at 25°C) in isopropanol-and Acetonitrilewater media at 35°C in the pH range, 7.2-8.9. It is of interest to note that the aquation rate constant of the conjugate base, cis-[Co(en)z(bzm)Cl]+ (Bzm = N -H deprotonated benzimidazole, en = ethylenediamine) is virtually insensitive to the compositions of the mixed solvents studied, unlike the aquation rate constant of the conjugate acid form of the title complex. This is indicative of a true dissociative mode of activation (Deb) of the conjugate base.
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