新型蓝光材料9,9'-联蒽衍生物的合成及其光电性能

安永; 徐茂梁; 王子俊; 安忠维; 弥阳丽; 田杰; 姜菡雨

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新型蓝光材料9,9'-联蒽衍生物的合成及其光电性能

材料合成及性能研究 | 更新时间：2020-08-12

- 新型蓝光材料9,9'-联蒽衍生物的合成及其光电性能
- Synthesis of Novel Blue Light Emitting 9,9'-bianthracene Derivatives and Their Optoelectronic Properties
- 发光学报 2011年32卷第9期页码：890-895
- 作者机构：
  
  西安近代化学研究所
- 作者简介：
- 基金信息：
  
  西安近代化学研究所民品青年创新基金(08865)资助项目()
- DOI：
  中图分类号： TN383.1
- 收稿：2011-06-22，
  
  修回：2011-7-15，
  
  网络首发：2011-09-22，
  
  纸质出版：2011-09-22
- 稿件说明：
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安永, 徐茂梁, 王子俊, 安忠维, 弥阳丽, 田杰, 姜菡雨. 新型蓝光材料9,9'-联蒽衍生物的合成及其光电性能[J]. 发光学报, 2011,32(9): 890-895

AN Yong, XU Mao-liang, WANG Zi-jun, AN Zhong-wei, MI Yang-li, TIAN Jie, JIANG Han-yu. Synthesis of Novel Blue Light Emitting 9,9'-bianthracene Derivatives and Their Optoelectronic Properties[J]. Chinese Journal of Luminescence, 2011,32(9): 890-895
安永, 徐茂梁, 王子俊, 安忠维, 弥阳丽, 田杰, 姜菡雨. 新型蓝光材料9,9'-联蒽衍生物的合成及其光电性能[J]. 发光学报, 2011,32(9): 890-895 DOI：

AN Yong, XU Mao-liang, WANG Zi-jun, AN Zhong-wei, MI Yang-li, TIAN Jie, JIANG Han-yu. Synthesis of Novel Blue Light Emitting 9,9'-bianthracene Derivatives and Their Optoelectronic Properties[J]. Chinese Journal of Luminescence, 2011,32(9): 890-895 DOI：

摘要

通过引入不同的取代基

采用Suzuki偶联反应

合成了一系列9

9'-联蒽衍生物新型蓝光材料

并研究了它们的紫外-可见吸收、荧光发射、荧光量子效率和电化学等性能。研究结果表明

这些化合物在二氯甲烷中均发射蓝色荧光

与9

9'-联蒽相比

其荧光发射峰均红移了7 nm

达到453 nm

是典型的蓝色荧光

同时也具有较高的荧光量子效率。

Abstract

paper

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Keywords

references

Friend R H, Gymer R W, Holmes A B, et al. Electroluminescence in conjugated polymers [J]. Nature, 1999, 397 (6715):121-128.[2] Tang C W, Vanslyke S A. Organic electroluminescent devices [J]. Appl. Phys. Lett., 1987, 51 (12):913-915.[3] Zhao Ting, Ding Hongbo, Shi Guoyue, et al. Organic light-emitting diodes using cascade energy transfer process [J]. Chin. J. Lumin. (发光学报), 2009, 30 (6):332-336 (in Chinese).[4] Xiong Zhiyong, Li Hongjian, Wang Junxi, et al. Optical characteristics of flexible microcavity organic light-emitting diodes [J]. Chin. J. Lumin. (发光学报), 2009, 30 (3):337-343 (in Chinese).[5] Yue Shumei, Li Na, Wang Binbin, et al. Syntheses, properties of luminescent complexes with 2-(2-pyridyl)benzimi-dazole ligands [J]. Chin. J. Lumin. (发光学报), 2009, 30 (6):852-857 (in Chinese).[6] Zhou Rui, Song Xinchao, Tian Jie, et al. Synthesis and spectroscopic properties of new blue-phosphorescent iridium complexes based on 2-difluorophenyl-4-methylpyridine and 2-(pyridyl-2-yl) imidazole as ligands [J]. Chin. J. Lumin. (发光学报), 2010, 31 (2):279-284 (in Chinese).[7] Wang Zhen, Chen Shuangwen, Zhou Xiang. Study on efficient blue and white organic light-emitting devices [J]. Chin. J. Lumin. (发光学报), 2010, 32 (7):715-719 (in Chinese).[8] Sun Li, Shao Xibin, Qin Lei, et al. Emission of electroplex in PVK and its properties under UV irradiation [J]. Chin. J. Lumin. (发光学报), 2010, 31 (6):332-336 (in Chinese).[9] Tao S L, Hong Z R, Peng Z K, et al. Anthracene derivative for a non-doped blue-emitting organic electroluminescence device with both excellent color purity high efficiency [J]. Chem. Phys. Lett., 2004, 397 (1):1-4.[10] Wang Zhiqiang, Zhu Yanyan, Huang Da, et al. Synthesis and characterization of the soluble blue-light emitting material 2-tert-butyl-9,10-bis(9,9-Dipropylfuorenyl) anthracene [J]. Photographic Science and Photochemistry (感光化学与光化学), 2007, 25 (6):415-421 (in Chinese).[11] Feng Liheng, Wang Xiaoju, Chen Zhaobin. Anthracene electroluminescence material containing cavity transmission group and preparation method: China,CN101144012A . 2008-03-19.[12] Tu Kexu, Wu Youyu, Zhang Xuhui, et al. A new type of blue light material 9,9-bianthracene and the application in OLED //Sixteenth National Conference on Semiconductor Physics, Lanzhou, Chinese Physical Society, 2007 (in Chinese).[13] Matsunami Shigeyuki, Sakamoto Yukisaku, Miyabayashi Yoshihisa. Bianthracene derivative, organic electroluminescent device, and display device: Japan, JP2006282533A . 2006-10-19.[14] Tian Jie, Wang Zijun, Song Xinchao, et al. Improved synthetic process of 10,10,-dibromo-9, 9,-bianthracene [J]. Applied Chemical Industry (应用化工), 2010, 39 (10):1607-1608 (in Chinese).[15] Brown H C, Colete T E. A simple preparation of boronic esters from organolithium reagents and selected trialkoxyboranes [J]. Organometallics, 1983, 2 (10):1316-1319.[16] Miyaura N, Suzuki A. Palladium-catalyzed cross-coupling reactions of organoboron compo- unds [J]. Chem. Rev., 1995, 95 (7):2457-2483.[17] Okumoto Kenji, Hamada Yuji. Organic electroluminescence element and organic electro- luminescent display device:Japan,JP2007150191A . 2007-06-14.[18] Yun H K, Hyun C J, Sung H K, et al. High purity-blue and high efficiency electroluminescent devices based on anthracene [J]. Adv. Funct. Mater., 2005, 15 (11):1799-1805.[19] Cummings S D, Eisenberg R. Tuning the excited-state properties of platinum(Ⅱ) diimine dithiolate complexes [J]. J. Am. Chem. Soc., 1996, 118 (8):1949-1960.[20] Wang Geyang. Synthesis and optical property of polymer containing β-diketone ligands . Xi'an: China Research and Development Academy of Machinery Equipment, 2009 (in Chinese).

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