Catalytic Kinetics of the Schiff Base Metal Complexes Bearing Side Chain of Cyclic morpholine in Carboxylic Ester Hydrolysis

It has been reported that two Schiff base transition metal complexes bearing the side chain of the morpholine ring were synthesized and characterized, and two complexes with the same base agent but different metal ions were used as a simulant hydrolase in the catalytic hydrolysis of p-nitrophenyl pi...

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Published inChinese journal of chemistry Vol. 25; no. 6; pp. 736 - 742
Main Author 张述林 李敏娇 欧忠文 陈国需 刘富安 谢家庆
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 01.06.2007
WILEY‐VCH Verlag
Wiley
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ISSN1001-604X
1614-7065
DOI10.1002/cjoc.200790137

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Summary:It has been reported that two Schiff base transition metal complexes bearing the side chain of the morpholine ring were synthesized and characterized, and two complexes with the same base agent but different metal ions were used as a simulant hydrolase in the catalytic hydrolysis of p-nitrophenyl picolinate in this paper. The mechanism of PNPP catalytic hydrolysis is proposed and supported by the results of the spectral analysis and the kinetic calculation. A kinetic mathematical model, applied to the calculation of the kinetic and thermodynamics parameters of PNPP catalytic hydrolysis, has been established on the foundation of the mechanism proposed. The result of the study shows that the two complexes have a good catalytic activity in PNPP catalytic hydrolysis, and the rate of the PNPP catalytic hydrolysis was increased with the increase of the pH values in the buffer solution and affected by the polarization effect of metal ion of the complexes.
Bibliography:31-1547/O6
O625.632
Schiff base complex, simulative hydrolase, synthesis, PNPP hydrolysis, catalytic kinetics
O621.256.5
the National Natural Science Foundation of China - No. 50572121
ark:/67375/WNG-V3P27TDP-Q
ArticleID:CJOC200790137
the Science Fund of the Sichuan Province Educational Department of China - No. 2005A145
istex:A8AFCA30899CFB351E957B8BB635C3BC398EFEF4
ISSN:1001-604X
1614-7065
DOI:10.1002/cjoc.200790137