Synthesis and characterization of fluorine-thiophene-based π-conjugated polymers using coupling reaction

被引:27
|
作者
Lee, Jang Yong [1 ]
Kwon, Yoon Jung [2 ]
Woo, Je-Wan [3 ]
Moon, Doo Kyung [1 ]
机构
[1] Konkuk Univ, Dept Chem & Mat Engn, Seoul 143701, South Korea
[2] Konkuk Univ, Coll Engn, Dept Textile Engn, Seoul 143701, South Korea
[3] Sangmyung Univ, Coll Nat Sci, Seoul 110743, South Korea
关键词
Conjugated polymers; Light-emitting diodes (LED); Luminescence;
D O I
10.1016/j.jiec.2008.05.005
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A solution processible fluorine-thiophene-based copolymers, namely poly [2,7-bis(4-octyl-2-thienyl)-9,9-dioctylfluorene-co-alt-5,5'-(2,21 bithiophene)] (P1), poly [2,7-bis(3-octyl-2-thienyl)-9,9-dioctylfluorene-co-alt-5,5'-(2,2'-bithiophene)] (P2), poly[2,7-bis(3,3'-dioctyl-5,5'-bithien-2yl)-9,9'-dioctylfluorene-co-alt-5,5'-(2,2'-bithiophene)] (P3) were synthesized using Suzuki and Stille coupling reaction. The polymers showed weight loss starting around 400 degrees C indicative of good thermal stability. UV-vis properties and photoluminescence (PL) properties were investigated in toluene. P1, P2 and P3 exhibited the absorption maximum at 450, 428 and 435 nm. and their PL spectrum peaked at 587, 559 and 560 nm, respectively. And all polymers, PI, P2 and P3, showed electroluminescence (EL) spectrum peaked at 592, 595 and 607 nm in the range of orange red. The polymers were electrochemically active in oxidation regions. P3 especially showed high oxidation stabilities in 1.17 V vs. Ag/Ag+. And P1 and P3 showed higher crystallinity than P2, because they have a repeated unit of 3,3'''-dialkyl-quaterthiophene. (C) 2008 Published by Elsevier B.V. on behalf of The Korean Society of Industrial and Engineering Chemistry.
引用
收藏
页码:810 / 817
页数:8
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