期刊文献+

三苯胺多枝化合物的合成及其荧光性质

Synthesis and fluorescence of triphenylamine multibranch chromophores
下载PDF
导出
摘要 采用Heck反应合成了2个三苯胺多枝化合物N,N,N-三{5-(4-叔丁基苯基)-1,3,4-噁二唑-2-苯乙烯基-4-苯基}胺(化合物1)和N,N,N-三[4-{2-(3,5-二-[5-(4-叔丁基苯基)-1,3,4-噁二唑-2-]苯基}-1-乙烯基}苯基}胺(化合物2),并测定了它们的吸收光谱、单光子荧光光谱和双光子荧光光谱。化合物1和2在二氯甲烷溶液中单光子荧光发射峰分别位在536和487nm。在锁模Nd∶YAG激光器800nm激光照射下,化合物1和2发射出很强的双光子上转换荧光,其最大波长分别在541和518nm。 Two triphenylamine muhibranch chromophores N, N, N-tris-[4-(2-{ 4-[5-( 4-tert-butyl-phenyl)-1, 3,4- oxadiazol-2-yl]-phenyl}-vinyl)-phenyl]amine(1) and N, N, N-tris[4-{ 2-(3,5-di- { 5-[4-(tert-butyl) phenyl]-1,3, 4-oxadiazol-2-yl) phenyl)-1-ethenyl) phenyl] amine(2) were prepared using Heck reaction. The absorption, single photon excited fluorescence, two-photon excited fluorescence spectra have been recorded. Using 400nm excitation wavelength in CHCl2, the single-photon excited fluorescence of 1 is in the green region with a peak at 536nm and chromophore 2 in the blue region with a peak at 487 nm. The very strong frequency-upconverted fluorescence emission with the central wavelength at 541nm and 518nm in the solution of CHCl2 can be easily observed from chromophores 1-2 solution excited with a Nd. YAG pumped dye laser at the wavelength 800nm in CHCl2 at a concentration of 10^-2mol/L.
出处 《功能材料》 EI CAS CSCD 北大核心 2008年第6期957-960,964,共5页 Journal of Functional Materials
基金 国家自然科学基金资助项目(60678042) 东南大学科学基金资助项目(9207041399)
关键词 三苯胺多枝化合物 HECK反应 双光子荧光 trlphenylamlne mulUbranch chromophores Heck reaction two-photon excited fluorescecce
  • 相关文献

参考文献8

  • 1Huang P, Shen J, Pu S, et al. [J]. Journal of Materials Chemistry, 2006, 16: 850-857.
  • 2Bhaskar A, Ramakrishna, Lu Z, et al. [J]. J Am Chem Soc, 2006, 128: 11840-11849.
  • 3Morales A R, Belfield K D, Hales J M, et al. [J]. Chem Mater, 2006, 18: 4972-4980.
  • 4Du P, Zhu W, Xie Y, et al. [J]. Macromolecules, 2004, 37 : 4387-4398.
  • 5Wang Y, HeGS, Prasad P N, et al. [J]. J Am Chem Soc, 2005, 127: 10128-10129.
  • 6Lee H J, Sohn J, Hwang J, et al. [J]. Org Lett, 2004, 6(1): 47-50.
  • 7Thomas M, Said G, Olivier M, et al. [J]. Synthesis, 2005, 11: 1771-1774.
  • 8钱鹰,孟康,路志锋,黄维,吕昌贵,崔一平.[1,3,4]-噁二唑衍生物的固相合成及其线性、非线性光谱性质[J].功能材料,2007,38(8):1352-1355. 被引量:3

二级参考文献6

  • 1Porres L,Mongin O,Blanchard-Desce M.[J].Tetrahedron Letters,2006,47:1913-1917.
  • 2Bhaskar A,Guda R,Haley M M,et al.[J].J Am Chem Soc,2006,128:13972-13973.
  • 3Moralas A R,Belfield K D,Hales J M,et al.[J].Chem Mater,2006,18:4972-4980.
  • 4Huang P,Shen J,Pu S,et al.[J].J Mater Chem,2006,16:850-857.
  • 5Lee H J,Sohn J,Hwang J,et al.[J].Chem Mater,2004,16:456-465.
  • 6Kuo W,Hsiue G,Jeng R.[J].J Mater Chem,2002,12:868-878.

共引文献2

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