Acta Chimica Sinica ›› 2003, Vol. 61 ›› Issue (9): 1449-1454. Previous Articles     Next Articles

Original Articles



  1. 山东大学
  • 发布日期:2003-09-15

Synthesis, Structure and Photo-Physical Property of trans-2-[(4'-N, N-dimethylamino) styryl]-5-dimesitylborylthiophene

Liu Zhiqiang;Fang Qi;Wang Dong;Xue Gang;Cao Duxia;Yu Wentao;Xia Guangming   

  1. State Key Laboratory of Crystal Materials, Shangdong University
  • Published:2003-09-15

A new organic compound, trans-2-[( A'-N, iV-dimethylamino ) styryl ] -5-dimesitylborylthiophene (abbreviated as DMASBT, 5) with dimesitylboryl, dimethylamino and styryl-thiophene as electron acceptor, electron donor and conjugate bridge respectively, was synthesized. Its crystal structure determined by X-ray diffraction method indicates that the B-C bond between B atom and it bridge is obviously shorter than those of between B atom and mesityl groups. This remarkably strengthened B-C bonding can be regarded as an evidence of additional p-7t conjugation between the B atom and n bridge. The photo-physical properties of 5 in various solvents were studied in details. With the increasing of the polarity of solvents, the emission band of 5 will be remarkably red-shifted, its quantum yield will be increased and the lifetime will be lengthened. 5 Shows strong nonlinear absorption in the NIR band (750 ~ 850 nm) in the laser experiments in THF solution. Especially when it was irradiated by a femto-second laser at 800 nm, a strong up-converted green fluorescence in THF was observed.

Key words: BORANE, up-converted fluosescence, THIOPHENE P, XRD, QUANTUM YIELD

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