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篇目详细内容

【篇名】 Synthesis, spectroscopic, and electrochemical properties of two dyads consisted of tetrathiafulvalene and carbazole
【刊名】 Frontiers of Chemical Engineering in China
【刊名缩写】 Front. Chem. Eng. China
【ISSN】 1673-7369
【EISSN】 1673-7474
【DOI】 10.1007/s11705-009-0015-x
【出版社】 Higher Education Press and Springer-Verlag
【出版年】 2009
【卷期】 3 卷2期
【页码】 192-195 页,共 4 页
【作者】 Guoqiao LAI; Yibo LIU; Meijiang LI; Yongjia SHEN;
【关键词】 donor-σ-acceptor molecule; intramolecular charge transfer interaction; photo induced electron transfer; tetrathiafulvalene; carbazole

【摘要】
Two donor-σ-acceptor molecules containing tetrathiafulvalene (TTF) and carbazole moieties were synthesized by the reaction of 9-(4-bromo-butyl)-carbazole (1) with 2,6-bis(hexylthio)-3-(2-cyanoethylthio)-7-(methylthio)-tetrathiafulvalene (2) or 2,6-bis(2-cyanoethylthio)-3,7-bis(methylthio)tetrathiafulvalene (3) in the presence of CsOH·H2O, respectively. The structures of the molecules were characterized by 1H NMR, 13C NMR, MS, and elemental analyses. They showed negligible intramolecular charge-transfer interaction in their ground states as indicated by their UV-Vis spectroscopics and cyclic voltammetry results. Compared with carbazole, their fluorescence was strongly quenched, which implied that a photo induced electron transfer (PET) interaction between TTF and carbazole moieties occurred.
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