Studies on the Kinetics and Mechanism of Hydrolysis of p-nitrophenyl Picolinate (PNPP) by Unsymmetrical bis-Schiff Base Complexes with Aza-crown Ether or Morpholino Pendants

2006 ◽  
Vol 31 (4) ◽  
pp. 487-494 ◽  
Author(s):  
Jian-zhang Li ◽  
Bin Xu ◽  
Ying Wang ◽  
Shen-xin Li ◽  
Bo Zhou ◽  
...  
2008 ◽  
Vol 33 (5) ◽  
pp. 655-660 ◽  
Author(s):  
Jian-Zhang Li ◽  
Fa-Mei Feng ◽  
Bin Xu ◽  
Wei-Dong Jiang ◽  
Sheng-Ying Qin

2004 ◽  
Vol 29 (5) ◽  
pp. 488-494 ◽  
Author(s):  
Jian-zhang Li ◽  
Jia-qing Xie ◽  
Wei Zeng ◽  
Xiao-yao Wei ◽  
Bo Zhou ◽  
...  

2009 ◽  
Vol 2009 (6) ◽  
pp. 345-350 ◽  
Author(s):  
Xue-song Feng ◽  
Ying Tang ◽  
Jian-zhang Li ◽  
Jin Zhang ◽  
Sheng-ying Qin

2009 ◽  
Vol 27 (2) ◽  
pp. 372-378 ◽  
Author(s):  
Jianzhang LI ◽  
Weidong JIANG ◽  
Famei FENG ◽  
Bin XU ◽  
Wei HU ◽  
...  

2013 ◽  
Vol 343 ◽  
pp. 65-68
Author(s):  
Xiang Zheng ◽  
Jian Zhang Li ◽  
Sheng Tian Huang ◽  
Zhu Zhu Yang ◽  
Wei Hu

The unsymmetrical bis-Schiff base manganese complexes with either benzo-10-aza-crown ether pendants ( MnL1Cl, MnL2Cl) or morpholino pendant (MnL3Cl,MnL4Cl) have been employed as models for hydrolase by studying the hydrolysis reactions of p-nitrophenyl picolinate (PNPP). The effects of complex structures, reaction pH and reaction temperature on the rate of PNPP hydrolysis have been investigted. All four complexes exhibit high catalytic activity and the rate increases with pH increasing at 25 oC. The complexes of ligands containing a crown ether group exhibit higher catalytic activities than the non-crown analogues.


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