Kinetics of the catalytic hydrolysis of allyl chloride in the presence of metals of group VIII

1967 ◽  
Vol 9 (2) ◽  
pp. 204
Author(s):  
R FLEED
2021 ◽  
Vol 62 (3) ◽  
pp. 350-359
Author(s):  
S. I. Shabunya ◽  
V. G. Minkina ◽  
V. I. Kalinin ◽  
N. D. Sankir ◽  
C. T. Altaf

2007 ◽  
Vol 46 (4) ◽  
pp. 1120-1124 ◽  
Author(s):  
Qinglin Zhang ◽  
Ying Wu ◽  
Xiaolei Sun ◽  
Jeff Ortega

1945 ◽  
Vol 67 (10) ◽  
pp. 1730-1733 ◽  
Author(s):  
Lewis F. Hatch ◽  
Reedus Ray Estes

2009 ◽  
Vol 7 (3) ◽  
pp. 542-549 ◽  
Author(s):  
Bin Xu ◽  
Weidong Jiang ◽  
Jin Zhang ◽  
Guangyin Fan ◽  
Jianzhang Li

AbstractTwo mono-Schiff base Mn(III) complexes (MnL2Cl, L=L1 and L2) were synthesized and employed as artificial hydrolases in catalyzing the hydrolysis of p-nitrophenylpicolinate (PNPP) in Gemini 16-2-16 micellar solution. The effect of different micelles and their complex structures on the catalytic hydrolysis of PNPP is discussed in detail. The observations showed that MnL 22Cl exhibited higher catalytic activity over MnL 12Cl under a comparable condition, which confirmed that an open active centre is essential for modulating the activities of the two enzyme mimics. Moreover, under the conditions employed, hydrolytic rates of PNPP induced by these Mn(III) complexes were faster in Gemini 16-2-16 micelles than that in the micellar solution of cetyltrimethylammonium bromide (CTAB), a conventional analogue of Gemini 16-2-16.


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