期刊文献+

Novel triphenylamine-based two-photon absorption dyes including benzophenone parts

Novel triphenylamine-based two-photon absorption dyes including benzophenone parts
下载PDF
导出
摘要 New two-photon absorption dyes including benzophenone parts, p-N,N-diphenylamino-p'-phenacylstilbene (C1), 4,4-di-(4- benzoylstyrene)yltriphenylamine (C2) and 4,4',4'-tri(4-benzoylstyrene)yltriphenylamine (C3), were synthesized and characterized by ^1H NMR and elemental analysis. The ratio of the molar extinction coefficients of compounds was approximately equal to the ratio of the branch amount of the compounds, namely, C1:C2:C3 was 1:2:3. Extremely high fluorescence quantum yields were detected for these compounds. These molecules exhibited obvious two-photon upconcerted fluorescence as excited by 800 nm Ti:sapphire femtosecond laser. New two-photon absorption dyes including benzophenone parts, p-N,N-diphenylamino-p'-phenacylstilbene (C1), 4,4-di-(4- benzoylstyrene)yltriphenylamine (C2) and 4,4',4'-tri(4-benzoylstyrene)yltriphenylamine (C3), were synthesized and characterized by ^1H NMR and elemental analysis. The ratio of the molar extinction coefficients of compounds was approximately equal to the ratio of the branch amount of the compounds, namely, C1:C2:C3 was 1:2:3. Extremely high fluorescence quantum yields were detected for these compounds. These molecules exhibited obvious two-photon upconcerted fluorescence as excited by 800 nm Ti:sapphire femtosecond laser.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2009年第11期1279-1282,共4页 中国化学快报(英文版)
基金 support from National Natural Science Foundation of China(Nos. 20776165,20702065,20872184) "Key Foundation of Chongqing Science and Technology Commission"(No.CSTC 2008BA4020) "A Foundation for the Author of National Excellent Doctoral Dissertation of PR China(No.200735)"for financial support sponsored by the Scientific Research Foundation for the Returned Overseas Chinese Scholars,State Education Ministry as well(Nos.20071108- 1,20071108-5)
关键词 Synthesis SPECTROSCOPY Two-photon absorption BENZOPHENONE Synthesis Spectroscopy Two-photon absorption Benzophenone
  • 相关文献

参考文献12

  • 1B.H. Cumpston, S.P. Anathavel, S. Barlow, D.L. Dyer, J.E. Ehrlich, L.L. Erskine, A.A. Heikal, S.M. Kuebler, I.Y.S. Lee, D. McCord-Maughon, J. Qin, H. Rockel, M. Rumi, X.L. Wu, S.R. Marder, J.W. Perry, Nature 398 (1999) 51.
  • 2A. Doraiswmy, C. Jin, R.J. Narayan, E Mageswaran, E Mente, R. Modi, R. Auyeung, D.B. Chrisey, A. Ovsianikov, Acta Biomater. 2 (2006) 267.
  • 3T. Watanabe, M. Akiyama, K. Totani, S.M. Kuebler, E Stellacci, W. Wenseleers, K. Braun, S.R. Marder, J.W. Perry, Adv. Funct. Mater. 12 (2002) 611.
  • 4I J.D. Pitts, A.R. Howell, R. Taboada, I. Banerjee, J. Wang, S.L. Goodman, EJ. Campagnola, Photochem. Photobiol. 76 (2002) 135.
  • 5E Gupta, EE Markowicz, K. Baba, J. O'Reilly, M. Samoc, P.N. Prasad, Appl. Phys. Lett. 88 (2006) 213109.
  • 6C. Fernandez, G. Marti-Mestres, J. Ramos, H. Maillols, J. Pharmaceut. Biomed. Anal. 24 (1) (2000) 155.
  • 7T. Itoh, H.K. Hall, Macromolecules 23 (1990) 4879.
  • 8M. Fischer, Georges, J. Chem. Phys. Lett. 260 (1996) 115.
  • 9H. Gomer, H.J. Kuhn, Chapter in Advances in Photochemistry, John Wiley & Sons, Inc., New York, 2007, p. 19.
  • 10I Q. He, J.G. Cheng, F. Bai, Chin. Chem. Lett. 18 (8) (2007) 920.

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