Abstract

A family of copolymer hydrogels containing different mass percentages of vinylimidazole, acrylamide and N, N′-methylenebisacrylamide were used to bind copper(II) ions. The resultant copper-loaded gels demonstrated spectroscopic features that indicated copper was bound in a distorted square planar geometry. The hydrolysis activity of these the most active of these systems towards bis(3-nitrophenyl)phosphate at pH 8 was 2.78 × 10 −6 s −1, five orders of magnitude greater than the uncatalyzed reaction. While these systems obey Michaelis–Menten kinetics, they also subject both competitive and non-competitive inhibition from excess substrate and excess hydroxide due to constraints based in the coordination geometry of the copper(II) active sites.

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