Green electroluminescent polyfluorenes containing 1,8-naphthalimide moieties as color tuner

被引:27
|
作者
Mei, Chongyu
Tu, Guoli
Zhou, Quanguo
Cheng, Yanxiang [1 ]
Xie, Zhiyuan
Ma, Dongge
Geng, Yanhou
Wang, Lixiang
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
基金
中国国家自然科学基金;
关键词
light-emitting; polyfluorenes; 1,8-naphthalimides;
D O I
10.1016/j.polymer.2006.03.085
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A series of copolymers (CNPFs) containing low-band-gap 1,8-naphthalimide moieties as color tuner was prepared by a Yamamoto coupling reaction of 2,7-dibromo-9,9-dioctylfluorene (DBF) and different amount of 4-(3,6-dibromocarbazol-9-yl)-N-(4'-tert-butyl-phenyl)-1,8-naphthalimide (Br-CN) (0.05-1 mol% feed ratio). The light emitting properties of the resulting copolymers showed a heavy dependence on the feed ratio. In photoluminescence (PL) studies, an efficient color tuning through the Forster energy transfer mechanism was revealed from blue to green as the increase of Br-CN content, while in electroluminescence (EL) studies, the color tuning was found to go through a charge trapping mechanism. It was found that by introduction of a very small amount of Br-CN (0.1-0.5 mol%) into polyfluorene, the emission color can be tuned from blue to pure green with Commission International de l'Echairage (CIE) coordinates being (0.21, 0.42) and (0.21, 0.48). A green emitting EL single-layer device based on CNPF containing 0.1 mol% of Br-CN showed good performances with a low turn-on voltage of 4.2 V, a brightness of 9104 cd/m(2), the maximum luminous efficiency of 2.74 cd/A and the maximum power efficiency of 1.51 lm/W. To further improve the EL performances through balancing the charge trapping process, a copolymer (BCNPF05) derived from 0.5 mol% of a triarylamine-containing 413,6-bis-[4"-(4"'-bromophenyl-p-tolyl-amino)-phenyll-carbazol-9-yi)-N-(4'-tert-butyl-phenyl)-1,8-naphthalimide (Br-BCN) and 99.5mol% of 2,7-dibromo-9,9-dioctylfluorene was also prepared. As expected, a single layer EL device based on BCNPF05 exhibited better performances with 2 a brightness of 14228 cd/m(2), the maximum luminous efficiency of 4.53 cd/A and the maximum power efficiency of 1.57 Im/W. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4976 / 4984
页数:9
相关论文
共 50 条
  • [21] 1,8-naphthalimide hydroperoxides as novel intercalating DNA cleavers
    Tao, ZF
    Qian, XH
    Wei, DZ
    DYES AND PIGMENTS, 1996, 31 (03) : 245 - 251
  • [22] N-(2-Hydroxyethyl)-1,8-naphthalimide
    Sun, Jie
    Yuan, Ai-lin
    Wang, Hai-Bo
    Sun, Jie
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2009, 65 : O1210 - U1213
  • [23] The synthesis, properties and application of some 1,8-naphthalimide dyes
    Konstantinova, T
    Spirieva, A
    Petkova, T
    DYES AND PIGMENTS, 2000, 45 (02) : 125 - 129
  • [24] Synthesis of new polymerizable 1,8-naphthalimide dyes containing a 2-hydroxyphenylbenzotriazole fragment
    Bojinov, V
    Grabchev, I
    DYES AND PIGMENTS, 2003, 59 (03) : 277 - 283
  • [25] Fluorescence properties of dyad compounds containing 1,8-naphthalimide and 1,3,4-oxadiazole
    Tian, H
    Ni, WJ
    Su, JH
    Chen, KC
    JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1997, 109 (03) : 213 - 215
  • [26] Synthesis and characterization of color tunable, highly electroluminescent copolymers of polyfluorene by incorporating the N-phenyl-1,8-naphthalimide moiety into the main chain
    Gopikrishna, Peddaboodi
    Das, Dipjyoti
    Iyer, Parameswar Krishnan
    JOURNAL OF MATERIALS CHEMISTRY C, 2015, 3 (36) : 9318 - 9326
  • [27] N-(3-Thienylmethyl)-1,8-naphthalimide
    Shi, YQ
    Chen, B
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2006, 62 : O2200 - O2201
  • [28] Fluorescent 4-amino-1,8-naphthalimide Troger's bases possessing conjugated 4-amino-1,8-naphthalimide moieties and their potential fullerenes Host-Guest complexes
    Murphy, Samantha A.
    Kotova, Oxana
    Comby, Steve
    Gunnlaugsson, Thorfinnur
    RESULTS IN CHEMISTRY, 2021, 3
  • [29] Colorimetric fluoride sensor based on 1,8-naphthalimide derivatives
    Ren, Jun
    Wu, Zhen
    Zhou, Ying
    Li, Yan
    Xu, Zuxun
    DYES AND PIGMENTS, 2011, 91 (03) : 442 - 445
  • [30] The synthesis and fluorescence properties of novel 1,8-naphthalimide derivatives
    Tian, Zhidan
    Liu, Yunchang
    Tian, Baozhu
    Zhang, Jinlong
    RESEARCH ON CHEMICAL INTERMEDIATES, 2015, 41 (02) : 1157 - 1169