Novel gemini micelles from dimeric surfactants with oxyethylene spacer chain. Small angle neutron scattering and fluorescence studies

被引:111
作者
De, S
Aswal, VK
Goyal, PS
Bhattacharya, S [1 ]
机构
[1] Indian Inst Sci, Dept Organ Chem, Bangalore 560012, Karnataka, India
[2] Bhabha Atom Res Ctr, Div Solid State Phys, Bombay 400085, Maharashtra, India
[3] Jawaharlal Nehru Ctr Adv Sci Res, Chem Biol Unit, Bangalore 560064, Karnataka, India
关键词
D O I
10.1021/jp980836c
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
Three new gemini surfactants containing mono-, di-, and trioxyethylene spacer chains have been synthesized. Small angle neutron scattering (SANS) cross sections from the micellar aggregates of these dimeric amphiphiles Br-, n-C16H33NMe2+-CH2(CH2OCH2)(p)CH2-N+Me2-n-C16H33,Br-, (where p = 1, 2, and 3) in aqueous media (D2O) have been measured. The data have been analyzed using the Hayter and Penfold model for macro-ion solution to compute the interparticle structure factor S(Q) taking into account the screened Coulomb interactions between the dimeric micelles. The SANS analysis showed that the micellar morphology depends on both the nature and the length of the spacer unit. Detailed analysis of the data further indicates that the introduction of oxyethylene spacer is not sufficient enough to prevent looping of the spacer chain. Thus the average separation between the dimethylammonium ion headgroups is considerably lower than is expected from a fully extended conformation of the spacer chain. The micelles from these surfactants have also been characterized in terms of their critical micelle concentrations (cmc), microviscosities, and micropolarities on the basis of the information provided by micelle-solubilized fluorescent probes. These results indicate little difference in their micellar properties such as cmc, microviscosity, and micropolarity.
引用
收藏
页码:6152 / 6160
页数:9
相关论文
共 47 条
[1]   Small-angle neutron scattering study of micellar structures of dimeric surfactants [J].
Aswal, VK ;
De, S ;
Goyal, PS ;
Bhattacharya, S ;
Heenan, RK .
PHYSICAL REVIEW E, 1998, 57 (01) :776-783
[2]   EFFECT OF COUNTERION ON THE SIZE AND CHARGE OF ALKYLTRIMETHYLAMMONIUM HALIDE MICELLES AS A FUNCTION OF CHAIN-LENGTH AND CONCENTRATION AS DETERMINED BY SMALL-ANGLE NEUTRON-SCATTERING [J].
BERR, S ;
JONES, RRM ;
JOHNSON, JS .
JOURNAL OF PHYSICAL CHEMISTRY, 1992, 96 (13) :5611-5614
[3]   EFFECT OF ADDED SODIUM AND LITHIUM CHLORIDES ON INTERMICELLAR INTERACTIONS AND MICELLAR SIZE OF AQUEOUS DODECYL-SULFATE AGGREGATES AS DETERMINED BY SMALL-ANGLE NEUTRON-SCATTERING [J].
BERR, SS ;
JONES, RRM .
LANGMUIR, 1988, 4 (06) :1247-1251
[4]   Esterolytic reactivities of (dialkylamino)pyridine amphiphiles solubilized in different pseudo-three-component cationic microemulsions [J].
Bhattacharya, S ;
Snehalatha, K .
LANGMUIR, 1997, 13 (03) :378-384
[5]   Dialkylaminopyridine catalysed esterolysis of p-nitrophenyl alkanoates in different cationic microemulsions [J].
Bhattacharya, S ;
Snehalatha, K .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1996, (09) :2021-2025
[6]   Synthesis, redox and electrochemical properties of new anthraquinone-attached micelle- and vesicle-forming cationic amphiphiles [J].
Bhattacharya, S ;
Subramanian, M .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1996, (09) :2027-2034
[7]   Evidence for the formation of acylated or phosphorylated monoperoxyphthalates in the catalytic esterolytic reactions in cationic surfactant aggregates [J].
Bhattacharya, S ;
Snehalatha, K .
JOURNAL OF ORGANIC CHEMISTRY, 1997, 62 (07) :2198-2204
[8]   Synthesis and vesicle formation from novel pseudoglyceryl dimeric lipids. Evidence of formation of widely different membrane organizations with exceptional thermotropic properties [J].
Bhattacharya, S ;
De, S ;
George, SK .
CHEMICAL COMMUNICATIONS, 1997, (23) :2287-2288
[9]   The effects of cholesterol inclusion on the vesicular membranes of cationic lipids [J].
Bhattacharya, S ;
Haldar, S .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1996, 1283 (01) :21-30
[10]   Synthesis and esterolytic chemistry of some (dialkylamino)pyridine-functionalized micellar aggregates. Evidence of catalytic turnover [J].
Bhattacharya, S ;
Snehalatha, K .
LANGMUIR, 1995, 11 (12) :4653-4660