SYNTHESIS AND LANGMUIR-BLODGETT-FILM PROPERTIES OF SOME BIFUNCTIONAL TTF DERIVATIVES

被引:14
作者
TORMOS, GV [1 ]
CAVA, MP [1 ]
WU, XL [1 ]
MCKINLEY, AJ [1 ]
METZGER, RM [1 ]
机构
[1] UNIV ALABAMA,DEPT CHEM,BOX 870336,TUSCALOOSA,AL 35487
基金
美国国家科学基金会;
关键词
D O I
10.1016/0379-6779(92)90302-Y
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Three new tetra-substituted derivatives of the good one-electron donor tetrathiafulvalene (TTF, 1), namely, an asymmetrical diacid with two hexadecylthio groups (TTF(SC16)2(SCH2CO2H)2, 3), an asymmetrical diester with two hexadecylthio groups (TTF(SC16)2(SCH2CO2Me)2, 4) and a symmetrical derivative with four hexadecylthio groups (TTF(SC16)4, 11), have been prepared. These yield stable 'Pockels-Langmuir' (PL) monolayers at the air/water interface; some transfer well to a solid support as Langmuir-Blodgett (LB) films, when the strong electron acceptor 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane (TCNQF4) is also added to the air/water interface. However, TCNQF4 does not transfer onto the LB films. Iodine doping of LB multilayers of 4 yields moderate in-plane conductivity.
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收藏
页码:131 / 146
页数:16
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