高等学校化学学报 ›› 2004, Vol. 25 ›› Issue (1): 76.

• 研究论文 • 上一篇    下一篇

上转换荧光化合物DMSSB与CSSB的合成、结构与光物理性质

曹笃霞1, 方奇1, 王东1, 薛刚1, 于文涛1, 刘志强1, 周玉芳2   

  1. 1. 山东大学晶体材料国家重点实验室;
    2. 物理与微电子学院, 济南 250100
  • 收稿日期:2002-11-04 出版日期:2004-01-24 发布日期:2004-01-24
  • 通讯作者: 方 奇(1956年出生),男,教授,博士生导师,主要从事材料化学与晶体学研究.E-mail:fangqi@icm.sdu.edu.cn E-mail:fangqi@icm.sdu.edu.cn
  • 基金资助:

    国家自然科学基金(批准号:20172034);国家重点基础研究发展规划项目资助

Synthesis, Structure and Photo-physical Properties of Two Novel Compounds DMSSB and CSSB with Up-conversion Fluorescence

CAO Du-Xia1, FANG Qi1, WANG Dong1, XUE Gang1, YU Wen-Tao1, LIU Zhi-Qiang1, ZHOU Yu-Fang2   

  1. 1. State Key Laboratory of Crystal Materials;
    2. College of Physics and Microelectronics, Shandong University, Jinan 250100, China
  • Received:2002-11-04 Online:2004-01-24 Published:2004-01-24

摘要: 以苯并噻唑为电子受体,以双苯乙烯基为共轭桥链,分别以二甲基胺和咔唑为电子给体合成了2个新的有机化合物DMSSB(反式,反式-2-{4-[(4-N,N-二甲基胺)苯乙烯基]苯乙烯基}-1,3-苯并噻唑)和CSSB(反式,反式-2-{4-[(4-N-咔唑)苯乙烯基]苯乙烯基}-1,3-苯并噻唑).用X射线衍射方法测定了CSSB的晶体结构.用波长为800nm的激光激发时,DMSSB与CSSB在THF中分别发出强的上转换橙色(λmax=589nm)和蓝绿色荧光(λmax=488nm).2个化合物在不同溶剂中的光物理数据和理论计算结果表明,苯并噻唑基是一个很好的电子受体.

关键词: 苯并噻唑, 上转换荧光, 发射截面, DMSSB, CSSB

Abstract: Two novel organic compounds with benzothiazolyl as π electron acceptor, dimethylamino and carbazolyl respectively as π electron donor: DMSSB(trans, trans-2-{4-[4-(N,N-dimethylamino)styryl]styryl}-1,3-benzothiazole) and CSSB(trans, trans-2-{4-[(4-N-carbazolyl)styryl]styryl}-1,3-benzothiazole) were synthesized. The crystal structure of CSSB was determined by X-ray diffraction method. Pumped by 800 nm laser, DMSSB and CSSB respectively exhibited strong up-converted orange(λmax=589 nm) and blue-green(λmax=488 nm) fluorescence in THF, large two-photon absorption cross-section and large two-photon fluorescence emission cross-section. The photo-physical data in various solvents and theoretical calculation results indicate that benzothiazolyl is a good electron acceptor.

Key words: Benzothiazolyl, Up-converted fluorescence, Emission cross-section, DMSSB, CSSB

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