Bulletin of the Chemical Society of Japan
Online ISSN : 1348-0634
Print ISSN : 0009-2673
ISSN-L : 0009-2673
Kinetics and Mechanism of the Interaction of Iminodiacetate with cis-Tetraamminediaquacobalt(III) Ion in Acidic Media
Prabir BhattacharyaPradyot Banerjee
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1985 Volume 58 Issue 12 Pages 3593-3596

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Abstract

Kinetics of the reaction of iminodiacetate (Hida) with cis-tetraamminediaquacobalt(III) have been studied spectrophotometrically at pH 3.0–4.15, [iminodiacetate]T=0.03–0.4. mol dm−3, I=0.5 mol dm−3 (NaClO4), in the temperature range 30–50 °C. The reaction is governed by the rate law:
rate={k−1+k1[iminodiacetate]T}[complex],
where k−1 and k1 denote the reverse aquation and anation rate constants respectively. At 40 °C the k−1 values increase with pH and show a limiting tendency at pH≈4. The pH-anation rate profile indicates no reaction at pH<1.5 and in the range 3.5–3.9, k1 remains constant. The pH dependence on rate is expressed as k1=kAKAH/([H+]+KAH), where kA is the anation rate arising from the aqua complex ion and Hida species and KAH, the dissociation constant for the iminodiacetic acid. The value of kA at 40 °C=(5±0.02)×10−5 mol−1 dm3 s−1. The activation parameters, ΔH\ eweq and ΔS\ eweq for the anation step are 170±2 kJ mol−1 and 239±3 JK−1mol−1. The reaction is believed to operate through the initial complexation at the carboxylate end followed by a fast intramolecular proton transfer with simultaneous ring closure to form a chelated product. The complexation probably takes place through a dissociative interchange (Id) mechanism.

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