Abstract
The relative stabilities of the complexes of Pd dien2+, and of Pd Et4dien2+ with X, where dien = diethylenetriamine and Et4dien = 1,1,7,7-tetra-ethyldiethylenetriamine, have been measured in aqueous solution, for X = Cl, Br, I, and SCN. In terms of free energies, the class (b) character of the Pd dien2+ ion is moderate and slightly greater than that of the Pd Et4dien2+ ion. In terms of enthalpy changes, the class (b) character of Pd Et4dien2+ is much greater. The difference is explained in terms of opposing steric and electronic effects, the latter being slightly stronger. A combination of kinetic and thermodynamic data suggests that the greater steric hindrance of the sulphur-bonded ligand in Pd Et4dien SCN+ approximately balances the weaker Pd–NCS bonding involved in the isothiocyanato-form of the complex. Steric hindrance in the complex Pd Et4dienSCN+ is estimated to be approximately 6 kcal./mole greater than in the complex Pd Et4dienl+. Kinetic parameters are reported for the reversible aquation reactions of Pd Et4dienX+, where X = Cl, Br, and I, and approximate values for the stability constants at 24° are given.

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