期刊文献+

两个具有强双光子荧光的有机硼化合物 被引量:5

Two Organoboron Compounds with Strong Two-photon Excited Fluorescence
在线阅读 下载PDF
导出
摘要 以二米基硼为电子受体,苯乙烯基噻吩为共轭桥,合成了两个新的稳定的有机硼化合物:反式,反式-2-二米基硼-5-{2-[4-(2-噻吩乙烯基)苯基]乙烯基}噻吩(1)和反式,反式-1,4-二-[2-(5-二米基硼噻吩)乙烯基]苯(2).前者为不对称结构的偶极分子,后者为对称的A-π-A型四极分子.对称性不同的化合物表现出不同的双光子吸收性质.对于偶极分子1.单双光子吸收达到的激发态能级接近,而对于四极分子2,双光子吸收达到的激发态则比单光子吸收所达到的激发态高出0.35 eV.在波长为710到900 nm范围的飞秒脉冲激光激发下,化合物1和2在THF溶液中都可以发出很强的绿色上转换荧光(1,λmax=505 nm;2,λmax=513 nm)).用双光子荧光法测得A-π-A型化合物2在775 nm处的双光子吸收截面达1340GM. Two new stable organoboron compounds with dimesitylboryl group as electron acceptor and styrylthiophene as conjugated bridge have been synthesized, which are named trans,trans-2-dimesityl-boryl-5-(2-(4-(2-(thien-2-yl)vinyl)phenyl)vinyl)thiophene (1) and trans,trans-1,4-bis[2-(5-dimesitylboryl-thien-2-yl)vinyl]benzene (2). The former is asymmetrical dipolar molecule and the latter is symmetrical A-π-A type quadrupolar molecule. The compounds with different symmetry exhibit different two-photon absorption properties. To dipolar molecule 1, the energy levels of the excited states by single- and two-photon absorption processes are very close, but to quadrupolar molecule 2, the level of the excited state by two-photon absorption is about 0.35 eV higher than that by single-photon absorption. Pumped by laser pulses from 710 to 900 nm in femtosecond regime, both compounds 1 and 2 showed strong green up-converted fluorescence in THF solution with λmax=505 nm for 1 and λ=513 nm for 2. Under the excitation of 775 nm light, the two-photon absorption cross-section of 2 was measured to be 1340 GM by two-photon fluorescence method.
出处 《化学学报》 SCIE CAS CSCD 北大核心 2005年第15期1415-1420,共6页 Acta Chimica Sinica
基金 国家自然科学基金(Nos.20472044 20172034)高等学校骨干教师资助计划资助项目.
关键词 双光子吸收 有机硼化合物 双光子荧光法 上转换荧光 organoboron compound two-photon absorption up-converted fluorescence
  • 相关文献

参考文献1

二级参考文献17

  • 1Denk, W.; Strickler, J. H.; Webb, W. W. Science 1990,248, 73.
  • 2Ren, Y.; Fang, Q.; Yu, W.-T.; Lei, H.; Tian, Y.-P.;Jiang, M.-H.; Yang, Q.-C.; Mak, T. C. W. J. Mater.Chem. 2000, 10, 2025.
  • 3Parthenopoulos, D. A.; Rentzepis, P. M. Science 1989, 245,843.
  • 4Oudar, J. L.; Chemla, D. S. J. Chem. Phys. 1977, 66,2664.
  • 5Liu, Z.-Q.; Fang, Q.; Wang, D.; Cao, D.-X.; Xue, G.;Yu, W.-T.; Lei, H. Chem.-Eur. J. 2003, 9, 5074.
  • 6Dean, J. A. Lange'sHandbookofChemistry, 15thed., McGrawHill Companies Inc., New York, 1999.
  • 7Yuan, Z.; Collings, J. C.; Taylor, N. J.; Marder, T. B.;Jardin, C.; Hale, J. F. J. Solid State Chem. 2000, 154, 5.
  • 8Kannan, R.; He, G. S.; Yuan, L. X.; Xu, F.; Prasad, P.N.; Dombroskie, A. G.; Reinhardt, B. A.; Baur, J. W.;Vaia, R. A.; Tan, L.-S. Chem. Mater. 2001, 13, 1896.
  • 9Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G.E.; Robb, M. A.; Cheeseman, J. R.; Montgomery, J. A.;Vreven, J. T.; Kudin, K. N.; Burant, J. C.; Millarm, J. M.;Iyengar, S. S.; Tomasi, J.; Barone, V.; Mennucci, B.; Cossi,M.; Scalmani, G.; Rega, N.; Petersson, G. A.; Nakatsuji,H.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.;Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao,O.; Nakai, H.; Klene, M.; Li, X.; Knox, J. E.; Hratchian,H. P.; Cross, J. B.; Adamo, C.; Jaramillo, J.; Gompers,R.; Stratmann, R. E.; Yazyev, O.; Austin, A. J.; Cammi,R.; Pomelli, C.; Ochterski, J. W.; Ayala, P. Y.; Morokuma,K.; Voth, G. A.; Salvador, P.; Dannenberg, J. J.;Zakrzewski, V. G.; Dapprich, S.; Daniels, A. D.; Strain, M.C.; Farkas, O.; Malick, D. K.; Rabuck, A. D.;Raghavachari, K.; Foresman, J. B.; Ortiz, J. V.; Cui, Q.;Baboul, A. G.; Clifford, S.; Cioslowski, J.; Stefanov, B. B.;Liu, G.; Liashenko, A.; Piskorz, P.; Komaromi, I.; Martin,R. L.; Fox, D. J.; Keith, T.; Al-Laham, M. A.; Peng, C.Y.; Nanayakkara, A.; Challacombe, M.; Gill, P. M. W.;Johnson, B.; Chen, W.; Wong, M. W.; Gonzalez, C.; Pople,J. A. Gaussian 03, Revision A. 1, Gaussian, Inc., Pittsburgh PA, 2003.
  • 10Lee, C.; Yang, W.; Parr, R. G. Phys. Rev. B 1988, 37,785.

共引文献3

同被引文献84

引证文献5

二级引证文献30

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部