Kinetics of the solvolysis of trans‐dichlorotetra(4‐t‐butylpyridine)‐cobalt(III) ions in mixtures of water with methanol and with ethanol

Abstract

AbstractFor the solvolysis of Co(4‐t‐Bupy)4Cl2− ions in water + methanol and water + ethanol, log (rate constant) does not vary linearly with the reciprocal of the dielectric constant. The Gibbs free energy, the enthalpy, and the entropy of activation are insensitive to changes in the solvent composition in these mixtures, although a slight broad maximum in ΔH* and ΔS* probably exists at mole fractions of about 0.2 in water + ethanol. This contrasts with the extrema in ΔH* and ΔS* found with more hydrophobic alcohols used as cosolvents. However, the application of a Gibbs energy cycle to the solvolysis in water and in the mixtures shows that there is a differential effect of changes in solvent structure on the emergent solvated CoIII cation in the transition state and on Co(4‐t‐Bupy)4Cl2+ in the initial state. The stability of the former increases relative to that of the latter as the cosolvent content of the mixture rises. © 1995 John Wiley & Sons, Inc.