Large π-Conjugated Quinacridone Derivatives: Syntheses, Characterizations, Emission, and Charge Transport Properties

被引:24
|
作者
Chen, Weiping [1 ]
Tian, Kui [2 ]
Song, Xiaoxian [1 ]
Zhang, Zuolun [1 ]
Ye, Kaiqi [1 ]
Yu, Gui [2 ]
Wang, Yue [1 ]
机构
[1] Jilin Univ, Coll Chem, State Key Lab Supramol Struct & Mat, Changchun 130012, Peoples R China
[2] Chinese Acad Sci, Beijing Natl Lab Mol Sci, Inst Chem, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
HIGH-PERFORMANCE; ORGANIC SEMICONDUCTORS; POLYMERS; DIKETOPYRROLOPYRROLE; ACCEPTOR; DIIMIDE;
D O I
10.1021/acs.orglett.5b03155
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Two 11-ring-fused quinacridone derivatives, TTQA and DCNTTQA, have been synthesized by ferric chloride mediated cyclization and Knoevenagel reaction. Replacement of the carbonyl groups (in TTQA) with dicyanoethylene groups (in DCNTTQA) not only red-shifted the emission to the near-infrared region but also led to a nonplanar skeleton that significantly improved the solubility of DCNTTQA. Moreover, dicyanoethylene groups rendered DCNTTQA low-lying HOMO and LUMO levels. DCNTTQA-based solution-processed field-effect transistors showed a hole mobility up to 0.217 cm(2) V-1 s(-1).
引用
收藏
页码:6146 / 6149
页数:4
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