Application of direct (hetero)arylation in constructing conjugated small molecules and polymers for organic optoelectronic devices

被引：33
作者：
Wu, Wenting [1 ]
Xin, Hanshen [1 ]
Ge, Congwu [1 ]
Gao, Xike [1 ]
机构：
[1] Chinese Acad Sci, Shanghai Inst Organ Chem, Key Lab Synthet & Self Assembly Chem Organ Funct, 345 Lingling Rd, Shanghai 200032, Peoples R China
来源：
TETRAHEDRON LETTERS | 2017年 / 58卷 / 03期
关键词：
Direct arylation; Sustainable chemistry; Conjugated small molecules and polymers; Organic solar cells; Organic transistors; DIRECT ARYLATION POLYCONDENSATION; FIELD-EFFECT TRANSISTORS; THIN-FILM TRANSISTORS; CATALYZED DIRECT ARYLATION; C-H TRANSFORMATION; HIGH-PERFORMANCE; HIGH-MOBILITY; SOLAR-CELLS; NAPHTHALENE DIIMIDE; SYNTHETIC METHOD;
D O I：
10.1016/j.tetlet.2016.11.126
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Direct (hetero)arylation, as a sustainable, atom-economic and environmentally benign synthetic protocol compared to conventional coupling techniques, has been extensively applied to the sustainable preparation of it-conjugated materials for organic optoelectronic devices. In this review, we will highlight recent advances made in direct arylation for conjugated small molecules and polymers toward high performance organic optoelectronic devices. Some important insights in direct arylation for synthesizing organic optoelectronic materials are given, together with the challenges and outlook in this significant and hot research field. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码：175 / 184
页数：10
相关论文
共 72 条
[1]   Carboxylate-Assisted Transition-Metal-Catalyzed C-H Bond Functionalizations: Mechanism and Scope [J].
Ackermann, Lutz .
CHEMICAL REVIEWS, 2011, 111 (03) :1315-1345
[2]   Aryl-aryl bond formation by transition-metal-catalyzed direct arylation [J].
Alberico, Dino ;
Scott, Mark E. ;
Lautens, Mark .
CHEMICAL REVIEWS, 2007, 107 (01) :174-238
[3]   Organic semiconductors for solution-processable field-effect transistors (OFETs) [J].
Allard, Sybille ;
Forster, Michael ;
Souharce, Benjamin ;
Thiem, Heiko ;
Scherf, Ullrich .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (22) :4070-4098
[4]   Low-Cost Synthesis and Physical Characterization of Thieno[3,4-c]pyrrole-4,6-dione-Based Polymers [J].
Berrouard, Philippe ;
Dufresne, Stephane ;
Pron, Agnieszka ;
Veilleux, Justine ;
Leclerc, Mario .
JOURNAL OF ORGANIC CHEMISTRY, 2012, 77 (18) :8167-8173
[5]   Synthesis of 5-Alkyl[3,4-c]thienopyrrole-4,6-dione-Based Polymers by Direct Heteroarylation [J].
Berrouard, Philippe ;
Najari, Ahmed ;
Pron, Agnieszka ;
Gendron, David ;
Morin, Pierre-Olivier ;
Pouliot, Jean-Remi ;
Veilleux, Justine ;
Leclerc, Mario .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2012, 51 (09) :2068-2071
[6]   Thiazolo[5,4-d]thiazoles - promising building blocks in the synthesis of semiconductors for plastic electronics [J].
Bevk, David ;
Marin, Lidia ;
Lutsen, Laurence ;
Vanderzande, Dirk ;
Maes, Wouter .
RSC ADVANCES, 2013, 3 (29) :11418-11431
[7]   Defect Analysis of High Electron Mobility Diketopyrrolopyrrole Copolymers Made by Direct Arylation Polycondensation [J].
Broll, Sebastian ;
Nuebling, Fritz ;
Luzio, Alessandro ;
Lentzas, Dimitros ;
Komber, Hartmut ;
Caironi, Mario ;
Sommer, Michael .
MACROMOLECULES, 2015, 48 (20) :7481-7488
[8]   Direct (Hetero)arylation Polymerization: Trends and Perspectives [J].
Bura, Thomas ;
Blaskovits, J. Terence ;
Leclerc, Mario .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2016, 138 (32) :10056-10071
[9]   Linear Side Chains in Benzo[1,2-b:4,5-b′]dithiophene-Thieno[3,4-c]pyrrole-4,6-dione Polymers Direct Self-Assembly and Solar Cell Performance [J].
Cabanetos, Clement ;
El Labban, Abdulrahman ;
Bartelt, Jonathan A. ;
Douglas, Jessica D. ;
Mateker, William R. ;
Frechet, Jean M. J. ;
McGehee, Michael D. ;
Beaujuge, Pierre M. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (12) :4656-4659
[10]   Stille Polycondensation for Synthesis of Functional Materials [J].
Carsten, Bridget ;
He, Feng ;
Son, Hae Jung ;
Xu, Tao ;
Yu, Luping .
CHEMICAL REVIEWS, 2011, 111 (03) :1493-1528
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