Catalytic hydrolysis of phosphate esters in microemulsions. 4. p-Nitrophenyl diphenyl phosphate hydrolysis catalyzed by iodosobenzoate and some of its derivatives

1988 ◽  
Vol 92 (15) ◽  
pp. 4505-4510 ◽  
Author(s):  
Beth A. Burnside ◽  
Barry L. Knier ◽  
Raymond A. Mackay ◽  
H. Dupont Durst ◽  
Frederick R. Longo
1988 ◽  
Vol 53 (9) ◽  
pp. 2009-2011 ◽  
Author(s):  
Beth A. Burnside ◽  
Linda L. Szafraniec ◽  
Barry L. Knier ◽  
H. Dupont Durst ◽  
Raymond A. Mackay ◽  
...  

1988 ◽  
Vol 9 (5) ◽  
pp. 493-510 ◽  
Author(s):  
Raymond A. Mackay ◽  
Beth A. Burnside ◽  
Stephanie M. Garlick ◽  
Barry L. Knier ◽  
H. Dupont Durst ◽  
...  

1988 ◽  
Vol 17 (1) ◽  
pp. 77-81 ◽  
Author(s):  
Barry L. Knier ◽  
H. Dupont Durst ◽  
Beth A. Burnside ◽  
Raymond A. Mackay ◽  
Frederick R. Longo

1995 ◽  
Vol 60 (5) ◽  
pp. 883-893 ◽  
Author(s):  
František Hampl ◽  
Jiří Mazáč ◽  
František Liška ◽  
Jiří Šrogl ◽  
Lubomír Kábrt ◽  
...  

1-Methyl- (Ia - Id) and 1-dodecyl-2-, 3- and 4-hydroxyiminomethylpyridinium salts (Ie - Ih), as well as 1-methyl- (IIa) and 1-dodecyl-3-hydroxyiminomethylpyridazinium salts (IIb, IIc), were synthesized as catalysts for hydrolytic cleavage of organophosphates. The activities of the prepared catalysts were evaluated by measuring rate constants of hydrolysis of 4-nitrophenyl diphenyl phosphate (PNPDPP) under conditions of a pseudo-first-order reaction. The observed reactivity of pyridinium aldoximes Ia - Ih towards PNPDPP in neutral or slightly basic aqueous solutions (pH 7.2 and 7.8) depends on the acidity of the hydroxyimino group. The cleavage of PNPDPP is strongly accelerated in solutions of 1-dodecylhydroxyiminomethylpyridinium salts Ie - Ih above their critical micellar concentration (CMC). Considerable effect on the velocity of PNPDPP cleavage was observed when quaternary pyridinium aldoximes Ie - Ih were comicellized with inert cationic tenside hexadecyltrimethylammonium bromide (CTAB). 1-Dodecyl-3-hydroxyiminomethylpyridazinium salts IIb and IIc were unstable in aqueous solutions under the above-mentioned conditions.


2014 ◽  
Vol 68 (5) ◽  
Author(s):  
Ying Liu ◽  
Xiang-Guang Meng ◽  
Jian-Mei Li ◽  
Xiao-Hong Li ◽  
Wei-Feng Yu

AbstractPhosphate esters play an important role in genetic information transfer, cell signal transduction, energy transmission and metabolic processes of living beings. Efficient catalytic hydrolysis of phosphate esters is still an attractive and challenging problem. Here, a new 2-amino-N-dodecyl-3-(1H-imidazol-5-yl)propanamide (L2) surfactant was synthesized and its metallomicelles of La3+, Cu2+, Co2+, and Zn2+ complexes were used as mimic metalloenzymes to catalyze the hydrolysis of glucose-1-phosphate (G1P) in a buffer solution at 35°C. The metallomicelle systems can efficiently catalyze the hydrolysis of G1P. The rare-earth metallomicelle LaL2 has the highest catalytic activity compared with those of the transition metal micelles CuL2, CoL2, and ZnL2. Different association behaviors of metallomicelles and substrate G1P were proposed. The imidazole group might accelerate the hydrolysis by activating H2O associated with the metal into a metal-OH− group. A possible catalytic mechanism was also discussed.


1990 ◽  
Vol 135 (2) ◽  
pp. 508-519 ◽  
Author(s):  
Stephanie M Garlick ◽  
H.Dupont Durst ◽  
Raymond A Mackay ◽  
Keith G Haddaway ◽  
Frederick R Longo

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