Pseudophase model for reactivity in reverse micelles. The case of the water-promoted reaction between two lipophilic reagents, bromine and 1-octene, in AOT microemulsions

被引:30
作者
Blagoeva, IB
Gray, P
Ruasse, MF
机构
[1] UNIV PARIS 07,CNRS URA 34,ITODYS,F-75005 PARIS,FRANCE
[2] BULGARIAN ACAD SCI,INST ORGAN CHEM,SOFIA 1113,BULGARIA
关键词
D O I
10.1021/jp960772a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Kinetic investigation of 1-octene bromination in AOT-isooctane-water microemulsions (13 less than or equal to w = [H2O]/[AOT] less than or equal to 24 and 6 less than or equal to z = [IO]/[AOT] less than or equal to 57) shows that the reaction is first-order in alkene and first-order in bromine, as usually found in protic media. Although both reagents are mainly located in the isooctane phase (K-tr, transfer coefficients from isooctane to water, are 1.5 x 10(-5) and 8.8 x 10(-3) for alkene and bromine, respectively), bromination occurs in an aqueous microenvironment, as illustrated by the high sensitivity of the bromination rate to the water content of the microemulsion. A kinetic pseudophase model describes the rate constant dependence on microemulsion composition satisfactorily by assuming competition between reactions at the interface and in the aqueous phase. Reasonable values for the coefficients of reagent partition between the interface and the two microphases and for the local bromination rate constants are obtained from the kinetic equations derived from the model. In particular, spectroscopically observed AOT-bromine complexation is in agreement with the high bromine concentration at the interface (K-2, bromine partition coefficient from isooctane to interface, = 6.8). The water-phase bromination rate constant, k(w) = 1 x 10(8) M(-1) s(-1), is in the same range as that measured in bulk water. The lower limit for the interfacial rate constant, k(i), is 10(3) M(-1) s(-1), a value close to that observed in poorly aqueous methanal (MeOH/H2O = 95/5 v/v). These data are compared with those recently obtained in the same microemulsions for solvolysis, a reaction which, Like bromination, is water-promoted but supposed to take place at the interface only. The results are discussed in terms of the chemical properties of the water molecules encased in the microemulsion droplets.
引用
收藏
页码:12638 / 12643
页数:6
相关论文
共 50 条
[1]  
ALIOTTA F, 1992, PROG COLL POL SCI S, V89, P258
[2]   DYNAMICS OF EXCITED-STATE REACTIONS IN REVERSED MICELLES .2. PROTON-TRANSFER INVOLVING VARIOUS FLUORESCENT-PROBES ACCORDING TO THEIR SITES OF SOLUBILIZATION [J].
BARDEZ, E ;
MONNIER, E ;
VALEUR, B .
JOURNAL OF PHYSICAL CHEMISTRY, 1985, 89 (23) :5031-5036
[3]   COMPARISON OF MOLECULAR BROMINE AND TRIBROMIDE ION AS BROMINATING REAGENTS .1. KINETIC EVIDENCE FOR DIFFERENT MECHANISMS OF ADDITION TO CYCLOHEXENE [J].
BELLUCCI, G ;
BIANCHINI, R ;
AMBROSETTI, R ;
INGROSSO, G .
JOURNAL OF ORGANIC CHEMISTRY, 1985, 50 (18) :3313-3318
[4]   INTERACTION OF IODINE WITH AEROSOL-OT IN REVERSED MICELLES IN N-HEXANE [J].
BIASUTTI, MA ;
SERENO, L ;
SILBER, JJ .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1994, 164 (02) :410-415
[5]  
BLOKZIJL W, 1993, ANGEW CHEM INT EDIT, V32, P1545, DOI 10.1002/anie.199315451
[6]   HYDROPHOBIC EFFECTS ON SIMPLE ORGANIC-REACTIONS IN WATER [J].
BRESLOW, R .
ACCOUNTS OF CHEMICAL RESEARCH, 1991, 24 (06) :159-164
[7]  
BRESLOW R, 1993, CHEM REV, V93, P2023
[8]   ION BINDING AND REACTIVITY AT CHARGED AQUEOUS INTERFACES [J].
BUNTON, CA ;
NOME, F ;
QUINA, FH ;
ROMSTED, LS .
ACCOUNTS OF CHEMICAL RESEARCH, 1991, 24 (12) :357-364
[9]  
Bunton CA., 1987, ADV PHYS ORG CHEM, V22, P213, DOI [10.1016/S0065-3160(08)60169-0, DOI 10.1016/S0065-3160(08)60169-0]
[10]   THE REACTION OF BROMINE WITH CYCLOHEXENE IN CARBON-TETRACHLORIDE .1. REACTIONS IN THE ABSENCE OF HYDROGEN BROMIDE - PRESENCE OF A SCAVENGER [J].
BYRNELL, CJA ;
COOMBES, RG ;
HART, LS ;
WHITING, MC .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1983, (08) :1079-1086