A NEW METHOD FOR ESTIMATING COUNTERION SELECTIVITY OF A CATIONIC ASSOCIATION COLLOID - TRAPPING OF INTERFACIAL CHLORIDE AND BROMIDE COUNTERIONS BY REACTION WITH MICELLAR BOUND ARYLDIAZONIUM SALTS

被引:58
作者
LOUGHLIN, JA [1 ]
ROMSTED, LS [1 ]
机构
[1] RUTGERS STATE UNIV,DEPT CHEM,WRIGHT RIEMAN LABS,NEW BRUNSWICK,NJ 08903
来源
COLLOIDS AND SURFACES | 1990年 / 48卷 / 1-3期
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
D O I
10.1016/0166-6622(90)80223-Q
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
Yields of aryl halides and phenolic products from dediazoniation of a hydrophobic aryldiazonium salt bound to cetyltrimethylammonium halide, CTAX, micelles in 0.1 to 0.2 M HX with added NaX(XCl- and Br-) are used to estimate, simultaneously, the quantity of halide counter-ions and water at the micelle surface. The interfacial counter-ion concentration increases, both in solutions of CTABr with added NaBr and CTACl with added NaCl with a proportionate decrease in interfacial water. The selectivity of CTAX micelles toward Br- and Cl- in solutions containing mixtures of the two ions is obtained directly, unlike all previous methods which require an estimate of the fraction of bound counter-ions. Counter-ion exchange constants, KBrCl, estimated from aryl bromide/aryl chloride yield ratios at high NaX, are consistent with published values. Our results show, for the first time, that KBrCl is insensitive to ionic strength up to 3.0 M NaX when [Br-]/[Cl-]=1.0, but has modest dependence on the mole fraction of Br- at constant total NaX. KBrCl is also independent of surfactant concentration, after correcting for the fraction of bound counter-ions. In principle, product ratios from reaction of hydrophobic aryldiazonium salts can be used to estimate the relative concentrations of all nucleophiles at the surfaces of association colloids, provided stable aryl substituted products are formed via rate determining loss of N2. © 1990.
引用
收藏
页码:123 / 137
页数:15
相关论文
共 45 条
[1]   QUENCHING OF AROMATIC HYDROCARBON FLUORESCENCE BY COUNTERIONS IN AQUEOUS MICELLAR SOLUTION - RELATIONSHIP TO ION-EXCHANGE [J].
ABUIN, E ;
LISSI, E ;
BIANCHI, N ;
MIOLA, L ;
QUINA, FH .
JOURNAL OF PHYSICAL CHEMISTRY, 1983, 87 (25) :5166-5172
[2]   COEXISTENCE OF ROD-LIKE AND GLOBULAR MICELLES IN THE CTAB-CTAC-H2O SYSTEM - EVIDENCE FROM THE FLUORESCENCE OF SOLUBILIZED PYRENE [J].
ALMGREN, M ;
LOFROTH, JE ;
RYDHOLM, R .
CHEMICAL PHYSICS LETTERS, 1979, 63 (02) :265-268
[3]  
[Anonymous], 1985, HYDROGENATION METHOD
[4]  
ARAUJO PS, 1983, J COLLOID INTERF SCI, V86, P293
[5]   NMR-STUDY OF THE LOCATION OF BROMIDE ION AND METHYL NAPHTHALENE-2-SULFONATE IN CATIONIC MICELLES - RELATION TO REACTIVITY [J].
BACALOGLU, R ;
BUNTON, CA ;
CERICHELLI, G ;
ORTEGA, F .
JOURNAL OF PHYSICAL CHEMISTRY, 1989, 93 (04) :1490-1497
[6]  
Balke S.T., 1984, QUANTITATIVE COLUMN
[7]   ASSOCIATION OF ANIONS TO CATIONIC MICELLES [J].
BARTET, D ;
GAMBOA, C ;
SEPULVEDA, L .
JOURNAL OF PHYSICAL CHEMISTRY, 1980, 84 (03) :272-275
[8]   A QUANTITATIVE TREATMENT OF MICELLAR EFFECTS UPON DEPROTONATION EQUILIBRIA [J].
BUNTON, CA ;
ROMSTED, LS ;
SEPULVEDA, L .
JOURNAL OF PHYSICAL CHEMISTRY, 1980, 84 (20) :2611-2618
[9]   IONIC COMPETITION IN MICELLAR REACTIONS - A QUANTITATIVE TREATMENT [J].
BUNTON, CA ;
MOFFATT, JR .
JOURNAL OF PHYSICAL CHEMISTRY, 1986, 90 (04) :538-541
[10]  
Bunton CA., 1986, ADV PHYS ORG CHEM, V22, P213, DOI DOI 10.1016/S0065-3160(08)60169-0