期刊文献+

以3-乙酰基樟脑作为辅助配体的环金属铱配合物的合成及光电性能研究 被引量:6

Synthesis and Photoelectric Property of Bis-Cyclometalated Iridium Complexes with 3-Acetyl Camphor as the Ancillary Ligand
原文传递
导出
摘要 以立体位阻3-乙酰基樟脑为辅助配体合成了系列新型的环金属铱配合物3-乙酰基樟脑-2-(2,4-二氟)苯基吡啶环金属铱配合物[(46dfppy)2Ir(acam)],3-乙酰基樟脑-2-苯基吡啶环金属铱配合物[(ppy)2Ir(acam)],3-乙酰基樟脑-2-苯并噻吩吡啶环金属铱配合物[(btp)2Ir(acam)].将配合物的吸收光谱、光致发光光谱以及光致发光效率与辅助配体为乙酰丙酮(acac)的对应配合物进行了比较,发现在配合物中引入具有大空间位阻的3-乙酰基樟脑使配合物的光致发光效率均有所提高.并将(ppy)2Ir(acam)用于有机电致发光器件,电致发光光谱在516 nm处有一最大强度峰,驱动电压为12 V时最大亮度为10930 cd/m2,最大亮度效率达到14.6 cd/A,电压为10.7 V时最大功率为4.23 lm/W,亮度为698 cd/m2. A series of bis-cyclometalated iridium complexes,iridium(III) bis(2-(2,4-difluoro)phenylpyridine-N,C2') 3-acetyl camphor [(46dfppy)2Ir(acam)],iridium(III) bis(2-phenylpyridinato-N,C2') 3-acetyl camphor [(ppy)2Ir(acam)] and iridium(III) bis(2-(2'-benzothienyl) pyridinato-N,C3') 3-acetyl camphor [(btp)2Ir(acam)] were synthesized with sterically 3-acetyl camphor as ancillary ligand.The absorption spectrum,PL spectra and photoluminescence efficiency of complexes were compared with the corresponding complexes with acetylacetone(acac) as the ancillary ligand.It was found that all of their photoluminescence efficiency could be improved when sterically hindered 3-acetyl camphor was introduced.When [(ppy)2Ir(acam)] was used as light-emitting devices,the EL spectra has the largest peak intensity at 516 nm.The device has the greatest brightness of 10930 cd/m2 and maximum brightness efficiency of 14.6 cd/A at 12 V.The highest power effciency and brightness are 4.23 lm/W and 698 cd/m2 respectively at 10.7 V.
出处 《化学学报》 SCIE CAS CSCD 北大核心 2012年第8期1028-1034,共7页 Acta Chimica Sinica
基金 国家自然科学基金(Nos.21072141 21172161 50973067 51173115)资助项目~~
关键词 环金属铱配合物 3-乙酰基樟脑 量子效率 bis-cyclometalated iridium complexes 3-acetyl camphor quantum efficiency
  • 相关文献

参考文献19

  • 1Chou, E T.; Chi, Y. J. Chem. Eur. J. 2007, 13, 380.
  • 2Wong, W. Y.; Zhou, G. J.; Yu, X. M.; Kwok, H. S.; Tang, B. Z. Adv. Funct. Mater. 2006, 16, 838.
  • 3Song, Y. H.; Yeh, S. J.; Chen, C. T.; Chi, Y.; Liu, C. S.; Yu, J. K.; Hu, Y. H.; Chou, P. T.; Peng, S. M.; Lee, G. H. Adv.Funct. Mater. 2004, 14, 1221.
  • 4Song, Y. H.; Chiu, Y. C.; Chi, Y. J. Chem. Eur. J. 2008, 14, 5423.
  • 5Yang, C. L.; Zhang, X. W.; You, H.; Zhu, L. Y. Adv. Funct. Mater. 2007, 17, 651.
  • 6Park, Y. S.; Kang, J. W.; Kang, D. M. Adv. Mater. 2008, 20, 1957.
  • 7Williams, E. L.; Haavisto, K.; Li, J.; Jabbour, G. E. Adv, Mater. 2007, 19, 197.
  • 8Ulbricht, C.; Beyer, B.; Fricbe, C.; Winter, A.; Schubert, U. S. Adv. Mater. 2009, 21, 4418.
  • 9Ho, C. L.; Wong, W. Y.; Wang, Q.; Ma, D. G; Wang, L. X.; Lin, Z. Y. Adv. Funct. Mater. 2008, 18, 928.
  • 10Ho, C. L.; Wong, W. Y.; Zhou, G. J.; Yao, B.; Xie, Z. Y.; Wang, L. X. Adv. Funct. Mater. 2007, 17, 2925.

同被引文献99

  • 1陶鹏,赵强,景姝,汪静霞,吕壮,陈柳青,王华.一种橙光磷光铱(Ⅲ)配合物的合成、晶体结构及光电性质研究[J].发光学报,2013,34(7):816-823. 被引量:2
  • 2林朝阳,赵鑫,戚裕,戴国梁.一种苯并咪唑类双极性蓝色磷光主体材料的合成及性能[J].化学通报,2015,78(4):342-346. 被引量:3
  • 3骆开均,徐玲玲,魏孝强,谢明贵,蒋青.微波法快速合成环金属铂配合物磷光发光材料[J].化学研究与应用,2007,19(9):991-993. 被引量:1
  • 4Shirota Y. Photo-and electroactive amorphous molecular materials-molecular design, syntheses, reactions, proper- ties, and applications[ J]. J Mater Chem ,2005,15:75-93.
  • 5Duan L, Hou L, Lee T W, et al. Solution processable small molecules for organic light-emitting diodes [ J ]. J Mater Chem,2010,20:6 392-6 407.
  • 6Fisher A L, Linton K E, Kamtekar K T, et al. Efficient deep-blue electroluminescence from an ambipolar emitter in a single-active layer device[ J]. Chem Mater, 2011,23 (7) :1 640-1 642.
  • 7Xiao L X, Chen Z J, Qu B, et al. Recent progresses on ma- terials for electrophosphorescent organic light-emitting de- vices [ J ]. Adv Mater ,2011,23 ( 8 ) :926-952.
  • 8Yook K S, Lee J Y. Organic materials for deep blue phos- phorescent organic light-emitting diodes [ J ]. Adv Mater, 2011,24:3 169-3 190.
  • 9Shallcross R C, Zacharias P, K6hnen A, et al. Photochro- mic materials:photochromic transduction layers in organic memory elements [ J ]. Adv Mater, 2013,25 ( 3 ) :469-476.
  • 10Ooyama Y,Harima ~. Molecular designs and syntheses of organic dyes for dye-sensitized solar cells[ J]. Eur J Org Chem,2009 ,18 :2 903-2 934. ,2007,17 : 115-122.

引证文献6

二级引证文献7

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