期刊文献+

一种环金属铱、铂双核配合物的合成及光电性能

Synthesis and Photoelectric Properties of a Cyclometalated Iridium-Platinum Binuclear Complex
下载PDF
导出
摘要 设计合成了一种双核环金属铱,铂配合物二[N,N-2-(2,4-二氟苯基吡啶)C3,N1](吡啶甲酸)合铱(Ⅲ)-C6-[苯基吡啶-C3,N1](吡啶甲酸)合铂(Ⅱ)(FIr PPy Pt)。通过核磁共振仪、元素分析仪、紫外-可见吸收光谱仪和光致发光光谱仪对其结构和性能进行了表征。结果表明,配合物FIr PPy Pt的紫外-可见吸收位于250~450 nm之间,荧光发射峰位于465和493 nm。将配合物FIr PPy Pt以质量分数1%~8%掺杂到主体材料聚乙烯基咔唑(PVK)+2-(联苯-4-芳基)-5-(4-叔丁基苯)-1,3,4-噁二唑(PBD)(30%)中制作了电致发光器件,在不同电压下电致发光光谱中,显现出铱配合物和铂配合物的特征峰,波峰位于400、500和530 nm蓝绿光区发射区。该双核配合物用于单掺杂有机白光电致发光器件具有制作简单、色稳定性和重复性好等特点,为单掺杂白光发光器件提供了一种好的思路。 A dinuclear cyclometalated iridium-platinum complex Iridium [Ⅲ]bis [( 2,4-difluorophenyl)-pyridinato-N,C2'][ picolinate]-C6-Paltinum[II][phenylpyridinato-N,C2'][picolinate ]( FIr PPy Pt) was designed and synthesized. Its structure and properties were characterized by NMR,elemental analyzer,UV absorption spectroscopy and photoluminescence spectroscopy. The results show that the UV absorption of the complex FIr PPy Pt is located between 250 and 450 nm,and the fluorescence emission peak is located at 465 and 493 nm. The electroluminescent devices were made from poly( N-vinylcarbazole)( PVK) + 2-( biphenyl-4-yl)-5-( 4-tert-butylphenyl)-1,3,4-oxadiazole( PBD) doped with 1% ~ 8% mass fraction of FIr PPy Pt complexes. The electroluminescence spectra at different voltages show the characteristic peaks of iridium complexes and platinum complexes located at 400,500 and 530 nm in blue-green emission zones. The dual core complexes are used for single doped organic white light emitting devices with simple fabrication,good color stability and good reproducibility,it provides a good idea for the single doped white light emitting devices.
出处 《应用化学》 CAS CSCD 北大核心 2016年第12期1428-1434,共7页 Chinese Journal of Applied Chemistry
基金 湖南省自然科学基金项目资助(14JJ2081)~~
关键词 铱配合物 铂配合物 有机电致发光器件 iridium complex platinum complex organic light emitting device
  • 相关文献

参考文献1

二级参考文献16

  • 1丁国华,荆淑萍,许兆武,徐仲玉,田禾,高佳,马东阁.橙红色磷光铱配合物的合成及其性能[J].应用化学,2005,22(5):502-506. 被引量:3
  • 2Baldo M A,O′Brien D F,You Y,et al.Highly Efficient Phosphorescent Emission from Organic Electroluminescent Devices[J].Nature,1998,395(6698):151-154.
  • 3Fan C H,Sun P,Su T H,et al.Host and Dopant Materials for Idealized Deep-Red Organic Electrophosphorescence Devices[J].Adv Mater,2011,23(26):2981-2985.
  • 4Tanaka D,Sasabe H,Li Y J,et al.Ultra High Efficiency Green Organic Light-Emitting Devices[J].Jpn J Appl Phys,2007,46(1/3):L10-L12.
  • 5Su S J,Gonmori E,Sasabe H,et al.Highly Efficient Organic Blue-and White-Light-Emitting Devices Having a Carrier-and Exciton-Confining Structure for Reduced Efficiency Roll-Off[J].Adv Mater,2008,20(21):4189-4194.
  • 6Tamayo A B,Alleyne B D,Djurovich P I,et al.Synthesis and Characterization of Facial and Meridional Tris-Cyclometalated Iridium(Ⅲ) Complexes[J].J Am Chem Soc,2003,125(24):7377-7387.
  • 7Yang C H,Fang K H,Chen C H,et al.High Efficiency mer-Iridium Complexes for Organic Light-Emitting Diodes[J].Chem Commun,2004,(19):2232-2233.
  • 8Holmes R J,Forrest S R,Sajoto T,et al.Saturated Deep Blue Organic Electrophosphorescence Using a Fluorine-Free Emitter[J].Appl Phys Lett,2005,87(24):243507.
  • 9Ding J Q,Gao J,Cheng Y X,et al.Highly Efficient Green-Emitting Phosphorescent Iridium Dendrimers Based on Carbazole Dendrons[J].Adv Funct Mater,2006,16(4):575-581.
  • 10Fehnel E A.Friedlander Syntheses with o-Aminoaryl Ketones.Ⅰ.Acid-Catalyzed Condensations of o-Aminobenzophenone with Ketones[J].J Org Chem,1966,31(9):2899-2902.

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