Immobilization of transition metal ion complexes and their catalytic activity towards the activation of hydrogen peroxide

Transition metal ion-imidazole complexes have been immobilized on silica, silica–alumina (25%Al2O3), and alumina supports by adsorption and functionalization methods. The catalytic activity of these supported complexes in the decomposition of H2O2 has been studied. The reaction exhibits first-order kinetics with respect to [H2O2] and the quantity of catalyst. The rate of reaction decreases as [H2O2]0 increases. The order of catalytic reactivity is strongly dependent on the type of metal ion, support, and the immobilization method. The complex anchored via adsorption exhibited a higher activity compared to the corresponding complex anchored via functionalization of the surface. The reaction proceed via formation of the peroxo-intermediate, which has an inhibiting effect on the reaction rate. The reaction is enthalpy-controlled as is concluded from the isokinetic relationship. A mechanism is proposed involving the generation of HO2• radicals from the peroxo-intermediate in the rate-determining step.