Mechanism of reaction of peroxomethyl radicals with copper(II)(glycine)2 and copper(II)(glycylglycylglycine) in aqueous solutions

The reactions of O2CH3 radicals with CuII(glycine)2 and CuII(GGG), GGG = glycylglycylglycine, in aqueous solutions were studied.The results demonstrate that the peroxyl radicals oxidize the copper complexes forming relatively stable intermediates of the type LmCuIII-OOCH3. These intermediates decompose via oxidation of the ligands glycine and GGG, respectively. Substituents on the alkyl of the peroxyl radical affect somewhat the kinetics of reaction but not the mechanism of oxidation. It is suggested that analogous reactions are probably contributing to the radical-induced deleterious biological processes.

The reactions of O2CH3 radicals with CuII(glycine)2 and CuII(GGG), GGG = glycylglycylglycine, forming relatively stable intermediates of the type LmCuIII-OOCH3, in aqueous solutions were studied. These intermediates decompose via oxidation of the ligands glycine and GGG, respectively. It is suggested that analogous reactions are probably contributing to the radical-induced deleterious biological processes.Figure optionsDownload as PowerPoint slide