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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;
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【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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