Abstract
Rate and activation parameters for the complex-formation reaction of Ni2+ with 4-(2-pyridylazo)-N, N-dimethyl aniline (PADA) were studied as a function of pH in different buffers in both aqueous and sodium dodecyl sulfate (SDS) micelle solutions. In aqueous Tris buffer solution, the forward and backward rate constants increased with increasing pH, while the complex-formation constant decreased due to a larger increase in the backward rate constant. The activation entropy, Delta S-#, and activation volume, Delta V-#, changed with increasing pH from positive to negative values, suggesting an apparent changeover from a dissociative to a more associative mechanism. Complex-formation reactions with 2,2'-bipyridine in Tris buffer showed almost no increase in the forward and backward rate constants on increasing the pH, but the Delta S-# and Delta V-# values became more negative. N-ethylmorpholine buffer showed no pH effect on the rate constants and activation parameters. Water exchange reactions of aquated Ni2+ were also studied as a function of pH under the same conditions. The reported rate and activation parameters for water exchange in Tris and N-ethylmorpholine buffers are consistent with those found for the complex-formation reactions of Ni2+ with PADA. The observed pH and buffer effects for both the complex-formation and water exchange reactions of aquated Ni2+ can be accounted for in terms of the formation of a Ni2+-Tris complex in Tris buffer and general base catalysis by the buffer components. In SDS micelle solution, the complex-formation reaction with PADA was much faster than in aqueous solution, but the increase in rate constant with increasing pH was less significant, while Delta S-# and Delta V-# became more positive, pointing to a more dissociative mechanism. For SDS micelle solutions there was no effect on the water exchange rate constant or activation volume. Mechanistic interpretations are offered for all observed pH, buffer and medium effects.