Nucleophilic Dephosphorylation of p-Nitrophenyl Diphenyl Phosphate in Cationic Micellar Media

The kinetics of nucleophilic dephosphorylation of p-nitrophenyl diphenyl phosphate by hydroxamate ions (R‘(CO)N(RO-)) have been investigated in aqueous cationic micellar media at pH 9.12 and 27 °C. The pseudo-first-order rate constant-surfactant profiles show micelle-assisted bimolecular reactions...

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Veröffentlicht in:Langmuir 2005-09, Vol.21 (19), p.8664-8669
Hauptverfasser: Ghosh, Kallol K, Sinha, Daliya, Satnami, Manmohan L, Dubey, D. K, Rodriguez-Dafonte, P, Mundhara, G. L
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container_issue 19
container_start_page 8664
container_title Langmuir
container_volume 21
creator Ghosh, Kallol K
Sinha, Daliya
Satnami, Manmohan L
Dubey, D. K
Rodriguez-Dafonte, P
Mundhara, G. L
description The kinetics of nucleophilic dephosphorylation of p-nitrophenyl diphenyl phosphate by hydroxamate ions (R‘(CO)N(RO-)) have been investigated in aqueous cationic micellar media at pH 9.12 and 27 °C. The pseudo-first-order rate constant-surfactant profiles show micelle-assisted bimolecular reactions involving interfacial ion exchange between bulk aqueous media and micellar pseudophase. N-Substituted hydroxamate ion shows higher reactivity over the unsubstituted hydroxamate ions in cationic micellar media. The kinetic data are discussed in terms of the pseudophase ion exchange model.
doi_str_mv 10.1021/la051223b
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subjects Cations - chemistry
Chemistry
Colloidal state and disperse state
Exact sciences and technology
General and physical chemistry
Hydrogen-Ion Concentration
Hydroxamic Acids - chemistry
Kinetics
Micelles
Micelles. Thin films
Models, Chemical
Molecular Structure
Nitro Compounds - chemistry
Phosphates - chemistry
Phosphorylation
Stereoisomerism
Water - chemistry
title Nucleophilic Dephosphorylation of p-Nitrophenyl Diphenyl Phosphate in Cationic Micellar Media
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