Volume 24, Issue 11 pp. 1498-1504
Full Paper

Studies on PNPP Hydrolysis Catalyzed by Schiff Base Cobalt(II) Complexes

Qin Xiao

Qin Xiao

Department of Chemistry, Sichuan University, Chengdu, Sichuan 610064, China

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Wei Hu

Wei Hu

Department of Chemistry, Sichuan University, Chengdu, Sichuan 610064, China

Department of Chemistry, Sichuan University of Science & Engineering, Zigong, Sichuan 643000, China

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Jian-Zhang Li

Jian-Zhang Li

Department of Chemistry, Sichuan University of Science & Engineering, Zigong, Sichuan 643000, China

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Ying Wang

Ying Wang

Department of Chemistry, Sichuan University of Science & Engineering, Zigong, Sichuan 643000, China

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Ci Li

Ci Li

College of Bioengineering, Chongqing Technology and Business University, Chongqing 400060, China

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Juan Du

Juan Du

Department of Chemistry, Sichuan University, Chengdu, Sichuan 610064, China

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Xiang-Guang Meng

Xiang-Guang Meng

Department of Chemistry, Sichuan University, Chengdu, Sichuan 610064, China

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Chang-Wei Hu

Chang-Wei Hu

Department of Chemistry, Sichuan University, Chengdu, Sichuan 610064, China

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Xian-Cheng Zeng
First published: 03 November 2006
Citations: 5

Abstract

Two cobalt(II) complexes of the Schiff base with morpholino or aza-crown ether pendants, CoL1 and CoL2, as mimic hydrolytic metalloenzyme, were used in catalytic hydrolysis of carboxylic ester (PNPP). The analysis of specific absorption spectra of the hydrolytic reaction systems indicates that key intermediates, made up of PNPP and Co(II) complexes, have been formed in reaction processes of the PNPP catalytic hydrolysis. The mechanism of PNPP catalytic hydrolysis has been proposed based on the analytic result of specific absorption spectrum. A kinetic mathematical model, applied to the calculation of the kinetic parameter of PNPP catalytic hydrolysis, has been established based on the mechanism proposed. The acid effect of buffer solution, structural effect of the complexes, and effect of temperature on the rate of PNPP hydrolysis catalyzed by the complexes have been also discussed.

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