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作 者:王丽颖[1] 任延志[1] 李薇[1] 曾广赋[1] 席时权[1]
机构地区:[1]中国科学院长春应用化学研究所,长春130022
出 处:《分析化学》1998年第4期466-469,共4页Chinese Journal of Analytical Chemistry
基 金:国家自然科学基金资助项目
摘 要:几种电子给体(四硫代富瓦烯,TTF)、电子受体(长链四氰基对二次甲基苯醌;C18 TCNQ)及它们相应的 1:1摩尔比复合物的气-液界面分子行为表明:不带长链的 TTC1- TTF、BEDT-TTF的成膜性在其与C18TCNQ形成复合物之后均得到显著改善。C16TTF、C18 TCNQ及两者不同结构LB膜组装体的紫外可见光谱研究发现:C18TCNQ在其单独的Y-型 膜中摩尔吸光系数是7.5×103,而在交替组装体中其摩尔吸光系数是1.3×103,给受体之间 的相互作用导致跃迁偶极矩减小,从而引起吸光系数减小4倍多。Investigations on molecular behavior of three kinds of derivatives of electron donor-tetrathiafulvalene (TTF ). electron acceptor-tetracyanoquinodimetha with long hy- drocarbon chain(C18TCNQ) and their complex with a molar ratio of 1: l at air-water inter- face show that, the interfaciaI properties of solid monolayers of TTC1-TTF and BEDT-TTF are improved greatly after forming complex with C18TCNQ. Both C16TTF and C18TCNQ have been investigated for solution phase and LB films structure by using ultraviolet-visible spectroscopies. The molar absorptivity E of C18TCNQ at 365 nm band differs considerably. In separate Y-type LB film of C18TCNQ, the ε is about 7. 5 × 103. However, in alternating depositions' structure with C16TTF, the ε is about l. 3 × 103. This result indicates that, the interaction between donor and acceptor leads the transition dipole moment of 365 nm to re- duce. The reduced transition dipole moment causes the absorptivity reduce.
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