研究简报

结构不对称三芳胺类化合物的合成、表征及性质研究

  • 李英俊 ,
  • 赵楠 ,
  • 李丽娜 ,
  • 李春燕 ,
  • 孙淑琴 ,
  • 周晓霞
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  • 辽宁师范大学化学化工学院 大连 116029

收稿日期: 2011-05-12

  修回日期: 2011-10-09

  网络出版日期: 2012-01-06

基金资助

辽宁省自然科学基金(No. 20102126)资助项目

Synthesis, Characterization and Properties of Some Novel Structural Asymmetric Triarylamines

  • Li Yingjun ,
  • Zhao Nan ,
  • Li Lina ,
  • Li Chunyan ,
  • Sun Shuqin ,
  • Zhou Xiaoxia
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  • College of Chemistry and Chemical Engineering, Liaoning Normal University, Dalian 116029

Received date: 2011-05-12

  Revised date: 2011-10-09

  Online published: 2012-01-06

Supported by

Project supported by the Natural Science Foundation of Liaoning Province (No. 20102126).

摘要

以二芳胺和3,5-二甲基碘苯为原料, 利用乌尔曼(Ullmann)反应, 合成出了4 个结构不对称三芳胺衍生物1~4,除了化合物1 之外均为新化合物. 利用IR, 1H NMR, 13C NMR, HRMS 和元素分析对其结构进行了表征. 考察了它们的光学、电化学和热稳定性质. 实验结果表明, 所合成的4 个目标化合物在氯仿稀溶液中发出绿色荧光, 具有良好的电化学和热稳定性. 所合成的目标化合物是潜在的空穴传输材料及发绿光的材料.

本文引用格式

李英俊 , 赵楠 , 李丽娜 , 李春燕 , 孙淑琴 , 周晓霞 . 结构不对称三芳胺类化合物的合成、表征及性质研究[J]. 有机化学, 2012 , 32(05) : 949 -952 . DOI: 10.6023/cjoc1105121

Abstract

Four structural asymmetric triarylamines were synthesized by diarylamines and 3,5-dimethyl-iodobenzene as the starting materials using Ullmann reaction. They are new compounds except the compound 1. The structures of the target compounds were characterized by IR, 1H NMR, 13C NMR, HRMS and elemental analysis. The optical, electrochemical, and thermal properties were examined. The results indicated that the synthesized compounds emitted green fluorescence in chloroform, and exhibited a good electrochemical and thermal stability. The synthesized triarylamines are potential hole-transporting materials and green-light-emitting materials.

参考文献

[1] Kurata, T.; Koshika, K.; Kato, F.; Kido, J.; Nishide, H. Polyhedron2007, 26, 1776.  

[2] Bellmann, E.; Shaheen, S. E.; Thayumanavan, S.; Barlow, S.;Grubbs, R. H.; Marder, S. R.; Kippelen, B.; Peyghambarian, N.Chem. Mater. 1998, 10, 1668.  

[3] Kim, Y. K.; Hwang, S. H. Synth. Met. 2006, 156, 1028.  

[4] Wang, Y.-G.; Ou, J.-B.; Xu, Q.-G.; Wu, L. Chin. J. Org. Chem.2006, 26(7), 992 (in Chinese).(王延广, 欧加保, 徐强国, 吴琳, 有机化学, 2006, 26(7), 992.)

[5] Shirota, Y. J. Mater. Chem. 2005, 15, 75.  

[6] Thelakkat, M. Macromol. Mater. Eng. 2002, 287, 442.  

[7] Bender, T. P.; Graham, J. F.; Duff, J. M. Chem. Mater. 2001, 13,4105.  

[8] Goodbrand, H. B.; Hu, N. X. J. Org. Chem. 1999, 64, 670.  

[9] J & K Chemical LTD Acros Organics Reference Handbook of FineChemicals, Beijing, 2006~2007, p. 1845.

[10] Promarak, V.; Ichikawa, M.; Meunmart, D.; Sudyoadsuk, T.;Saengsuwan, S.; Keawina, T. Tetrahedron Lett. 2006, 47, 8949.  

[11] Tan, C. X.; Feng, R. F.; Peng, X. X. Chin. Chem. Lett. 2007, 18,505.  

[12] Ding, B.-D.; Zhang, J.-M.; Zhu, W.-Q.; Zheng, X.-Y.; Wu, Y.-Z.;Jiang, X.-Y.; Zhang, Z.-L.; Xu, S.-H. Chin. J. Lumin. 2003, 24, 606(in Chinese).(丁邦东, 张积梅, 朱文清, 郑新友, 吴有智, 蒋雪茵, 张志林,许少鸿, 发光学报, 2003, 24, 606.)

[13] Tian, W.-J.; Wu, F.; Fan, Y.-G.; Shen, J.-C. Chin. J. Lumin. 2000,21, 230 (in Chinese).(田文晶, 吴芳, 樊玉国, 沈家骢, 发光学报, 2000, 21, 230.)
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