MONOLAYER FORMATION OF SYNTHETIC AMMONIUM AMPHIPHILES CARRYING CYANOBIPHENYLOXY MESOGENS

被引:16
作者
EVERAARS, MD [1 ]
MARCELIS, ATM [1 ]
SUDHOLTER, EJR [1 ]
机构
[1] WAGENINGEN UNIV AGR,ORGAN CHEM LAB,DREIJENPLEIN 8,6703 HB WAGENINGEN,NETHERLANDS
关键词
D O I
10.1016/0040-6090(94)90505-3
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
New amphotropic molecules 4-6 have been prepared and the monolayer properties have been investigated on a Langmuir trough. The results are compared with the monolayer properties of 1-3. At high area per molecule the amphotropic molecules lie flat on the aqueous surface and both the ammonium head group and the cyanobiphenyloxy mesogens interact with water. Upon compression the cyanobiphenyloxy alkyl moieties are expelled from the surface. The presence of an extra n-dodecyl chain in 4 and 5 does not affect the lift-off area, compared with 1 and 2. The higher pi(coex) observed for 4 and 5, compared with 1-3 and 6, is interpreted as stabilization of the monolayer in which the cyanobiphenyl mesogens still interact with water. The presence of a third mesogenic moiety in 6 results in a large increase in lift-off area. Transfer experiments of monolayers of 3 onto quartz substrates show that only one monolayer can be deposited during the upstroke movement. If the transfer is carried out from the solid monolayer phase, the presence of stacked H aggregates could be detected from the optical absorption spectra. In contact with water, this monolayer is not stable and reorganization is observed.
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页码:78 / 82
页数:5
相关论文
共 15 条
[1]   AGGREGATION BEHAVIOR OF DOUBLE-CHAINED AMMONIUM AMPHIPHILES CONTAINING (CYANOBIPHENYLYL)OXY UNITS [J].
EVERAARS, MD ;
MARCELIS, ATM ;
SUDHOLTER, EJR .
LANGMUIR, 1993, 9 (08) :1986-1989
[2]   CRYSTAL-STRUCTURES OF SELF-AGGREGATES OF INSOLUBLE ALIPHATIC AMPHIPHILIC MOLECULES AT THE AIR-WATER-INTERFACE - AN X-RAY SYNCHROTRON STUDY [J].
JACQUEMAIN, D ;
LEVEILLER, F ;
WEINBACH, SP ;
LAHAV, M ;
LEISEROWITZ, L ;
KJAER, K ;
ALSNIELSEN, J .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (20) :7684-7691
[3]  
KELLNER BMJ, 1979, CHEM PHYS LIPIDS, V23, P41, DOI 10.1016/0009-3084(79)90021-5
[4]   MONOLAYER STUDIES OF HYDROXYHEXADECANOIC ACIDS [J].
KELLNER, BMJ ;
CADENHEAD, DA .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1978, 63 (03) :452-460
[5]  
MACRITCHIE F, 1990, CHEM INTERFACES, P138
[6]   CHAIN-SUBSTITUTED LIPIDS IN MONOMOLECULAR FILMS - EFFECT OF POLAR SUBSTITUENTS ON MOLECULAR PACKING [J].
MENGER, FM ;
RICHARDSON, SD ;
WOOD, MG ;
SHERROD, MJ .
LANGMUIR, 1989, 5 (03) :833-838
[7]   CONFORMATION AND PHASE-TRANSITIONS IN MONOLAYERS OF SOME C18 FATTY-ACIDS CONTAINING A HYDRATABLE FUNCTIONAL-GROUP IN THEIR ALKYL CHAINS [J].
NAGARAJAN, MK ;
SHAH, JP .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1981, 80 (01) :7-19
[8]   ORIENTED FILMS FROM POLYMERIC AMPHIPHILES WITH MESOGENIC GROUPS - LANGMUIR-BLODGETT LIQUID-CRYSTALS [J].
PENNER, TL ;
SCHILDKRAUT, JS ;
RINGSDORF, H ;
SCHUSTER, A .
MACROMOLECULES, 1991, 24 (05) :1041-1049
[9]  
RAKAHIT AK, 1981, J COLLOID INTERF SCI, V80, P466
[10]  
RINGSDORF H, 1988, ANGEW CHEM, V100, P117