期刊文献+

具有圆偏振光特性的卟啉衍生物的合成、表征和CD光谱研究 被引量:2

Synthesis, Characterization and CD Spectrum of Porphyrin Derivatives with Circularly Polarized Property
在线阅读 下载PDF
导出
摘要 合成了一组不同碳链的胆甾醇酯侧链卟啉配体和金属Zn配合物.研究了它们的吸收光谱和发射光谱.将这些卟啉配体以一定浓度掺杂在聚甲基丙烯酸甲酯(PMMA)中制成固体薄膜,发现由于在卟啉环上引入了手性的胆甾醇酯侧链,卟啉化合物在soret带和Q带均有较强的CD吸收,这种现象可能是卟啉环上的四个手性胆甾醇酯侧链与四苯基卟啉环发生偶合作用.进一步还发现这些卟啉化合物的圆偏振吸收性质与在PMMA中的浓度有关. A series of porphyrin compounds and Zn complexes with cholesterol ester side chains were synthesized and their UV-Vis and fluorescence spectrum were tested. CD spectrum showed that these compounds in polymethyl methacrylate (PMMA) solid film had circular dichroism property in soret and Q bands because of mutual coupling between chiral cholesterol ester moieties and tetraphenylporphyrin ring, furthermore, it was found that the CD spectrum of cholesterol ester porphyrin compounds was changed along with concentration of these compounds in PMMA solid film.
出处 《化学学报》 SCIE CAS CSCD 北大核心 2007年第10期977-982,共6页 Acta Chimica Sinica
基金 国家自然科学基金(No.20472060)资助项目.
关键词 胆甾醇酯侧链 卟啉化合物 圆二色谱(CD) 圆偏振发光材料 cholesterol ester side chain porphyrin compound circular dichroism circularly polarized luminescence
  • 相关文献

参考文献13

  • 1Burrows,P.E.; Forrest,S.P.; Buey,J.; Hissler,M.Appl.Phys.Lett.1996,69,2959.
  • 2Baldo,M.A.; O'Beien,D.F.; You,Y.; Sheldrick,J.M.Nature 1998,395,151.
  • 3Sakakibara,Y.Appl.Phys.Lett.1999,74,2587.
  • 4Chen,S.H.; Katsis,D.Nature 1999,397,506.
  • 5Grell,M.;Bradley,D.D.C.Adv.Mater.1999,11(11),895.
  • 6O'Neill,M.; Stenphen,M.K.Adv.Mater.2003,15(14),1135.
  • 7Rachel,S.D.; Judith,A.H.; Janet,M.M.; Gray,H.B.Chem.Commun.1997,18,1012.
  • 8Meskers,S.C.J.; Peeters,E.; Langeveldvoss,B.M.W.Adv.Mater.2000,12(8),589.
  • 9Emiel,P.; Marwijn,P.T.J.Am.Chem.Soc.1997,119(41),9909.
  • 10骆开均,谢明贵,蒋青,邹德春.具有手性侧链的卟啉液晶化合物的合成和发光性能研究[J].化学学报,2004,62(24):2425-2430. 被引量:7

二级参考文献41

  • 1师宇华,八寻信英,柳巍,师同顺.四(对-十八酰氧基)苯基卟啉及其过渡金属配合物的合成及红外光声光谱研究[J].高等学校化学学报,2004,25(7):1194-1198. 被引量:4
  • 2付世涛,王凯,谢征,李早英.新型桥连双卟啉化合物的合成及结构表征[J].高等学校化学学报,2004,25(7):1204-1208. 被引量:16
  • 3Gentemann S., Medforth C. J., Foresyth T. P. et al.. J. Am. Chem. Soc.[J], 1994, 116: 7 363-7 368
  • 4DiMngao S. G., Wertsching A. K., Ross C. R.. J. Am. Chem. Soc.[J], 1995, 117: 8 279-8 280
  • 5Burrows P. E., Forrest S. R., Sibly S. P. et al.. Appl. Phys. Lett.[J], 1996, 69: 2 959-2 961
  • 6Hamada Y.. IEEE. Trans. Electron Devices[J], 1997, 44: 1 208-1 217
  • 7Baldo M. A., O′Brien D. F., You Y. et al.. Nature(London)[J], 1998, 395: 151-154
  • 8Sakakibara Y.. Appl. Phys. Lett.[J], 1999, 74: 2 587-2 589
  • 9Tang C. W., Van Slyke S. A.. Appl. Phys. Lett.[J], 1987, 51: 913-915
  • 10Gust D., Moore T. A., Liddell P. A.. J. Am. Chem. Soc.[J], 1987, 109: 846-856

共引文献50

同被引文献6

引证文献2

二级引证文献5

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