Abstract
Abstract Three new binuclear copper(II) complexes have been prepared with shift bases derived from the condensation of 2,6-diformyl-4-methylphenol with the amino acids lysine, glutamic acid and arginine. The binuclearity of the complexes was characterized from optical, magnetic and electron spin resonance studies. Their ability to catalyze the dioxygen oxidation of several substituted catechols was measured using oxygen uptake and optical techniques.
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