Kinetics and mechanism of reactions ofbis(biguanide)copper(II) ion with glycine and α-alanine in aqueous media
✍ Scribed by Asim K. Das
- Publisher
- Springer
- Year
- 1994
- Tongue
- English
- Weight
- 329 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0340-4285
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✦ Synopsis
The kinetics of the reaction of [Cu(bigH)2] 2+ (bigH = biguanide) with an excess of amino acid (LH), namely glycine or e-alanine, in aqueous solution in the 7.6-9.0 pH range at different temperatures (30-40~ have been followed by stopped-flow spectrophotometry. The ligand replacement process has been found to pass through intermediate formation of a ternary complex, [Cu(bigH)L] + at the slower step, followed by rapid transformation into the binary complex, [CuL2]. The overall ligand replacement process has a ligand dependent (kl) path which is first order with respect to the incoming ligand (L-), and a ligand independent (k0) path. Under pseudo-first order conditions containing excess amino acid, the experimental observations conform to the rate law koh ~ = k o + k~K,[L]r/ ([H +] + K~), where [LIT stands for the total concentration of amino acid and Ka gives the deprotonation constant of LH. The solvent assisted dissociation (i.e. k 0 path) leads to a copper(II) mono-biguanide complex followed by rapid nucleophilic substitution; the k~ path is in agreement with an associative mechanism. The activation parameters (AH e , AS ~ ) for each step have been determined.
📜 SIMILAR VOLUMES
Ninhydrin has been found to react with Cu(glycine)+ and Cu(alanine)+ in the ratio of 1:l. The kinetic studies of the reaction were carried out at different concentrations of the reactants at 80°C (pH = 5.0). The reaction proceeds through the formation of a ternary labile complex of ninhydrin with Cu
## Abstract The rates of reaction between ninhydrin and dipeptide glycyl–glycine (Gly–Gly) have been determined by studying the reaction spectrophotometrically at 70°C and pH 5.0 in aqueous and in aqueous cationic micelles of cetyltrimethylammonium bromide (CTAB). The reaction follows first‐ and fr