Issue 6, 1999

Dinuclear zinc(II) complex of a new acyclic phenol-based dinucleating ligand with four methoxyethyl chelating arms: first dizinc model with aminopeptidase function

Abstract

A new end-off type acyclic ligand with four methoxyethyl chelating arms, 2,6-bis[bis(2-methoxyethyl)aminomethyl]-4-methylphenol (Hbomp), formed a dinuclear zinc(II) complex [Zn2(bomp)(MeCO2)2]BPh4 1. X-Ray analysis revealed that the complex 1·CHCl3 contains two zinc ions bridged by the phenolic oxygen and two acetate groups, forming a µ-phenoxo-bis(µ-acetato)dizinc(II) core. The aminopeptidase function of complex 1 was estimated using N-p-nitrophenyl-L-leucine as substrate. The release of p-nitroaniline as the result of the substrate hydrolysis is first order in both complex and substrate concentrations with k = 2.3(1) × 10–3 dm3 mol–1 s–1.

Supplementary files

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1999, 997-1000

Dinuclear zinc(II) complex of a new acyclic phenol-based dinucleating ligand with four methoxyethyl chelating arms: first dizinc model with aminopeptidase function

H. Sakiyama, R. Mochizuki, A. Sugawara, M. Sakamoto, Y. Nishida and M. Yamasaki, J. Chem. Soc., Dalton Trans., 1999, 997 DOI: 10.1039/A808055K

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