Palladium-catalyzed C-H homocoupling of bromothiophene derivatives and synthetic application to well-defined oligothiophenes

被引:189
作者
Takahashi, Masabumi
Masui, Kentaro
Sekiguchi, Hiroki
Kobayashi, Nobuhiko
Mori, Atsunori
Funahashi, Masahiro
Tamaoki, Nobuyuki
机构
[1] Tokyo Inst Technol, Chem Resouces Lab, Yokohama, Kanagawa 2268503, Japan
[2] Natl Inst Adv Ind Sci & Technol, Tsukuba, Ibaraki 3058565, Japan
关键词
LONG OLIGOTHIOPHENES; COUPLING REACTIONS; POLYTHIOPHENES; CONSTRUCTION; THIOPHENES; ACTIVATOR; OLIGOMERS; POLYMERS; LENGTH;
D O I
10.1021/ja060749v
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Synthesis of oligothiophenes of well-defined structures that possess 2-8 thiophene units is performed with a new synthetic strategy involving C-H homocoupling of bromothiophenes and cross-coupling with organostannanes. Tolerance of the carbon-bromine bond to the palladium-catalyzed C-H homocoupling results in oligothiophenes bearing C-Br bonds at the terminal thiophene rings, which allow further transformation by the catalysis of a transition-metal complex.
引用
收藏
页码:10930 / 10933
页数:4
相关论文
共 36 条
[1]  
Ahmed MSM, 2005, B CHEM SOC JPN, V78, P160
[2]   REGIOCHEMISTRY AND CONFORMATION OF POLY(3-HEXYLTHIOPHENE) VIA THE SYNTHESIS AND THE SPECTROSCOPIC CHARACTERIZATION OF THE MODEL CONFIGURATIONAL TRIADS [J].
BARBARELLA, G ;
BONGINI, A ;
ZAMBIANCHI, M .
MACROMOLECULES, 1994, 27 (11) :3039-3045
[3]   OLIGOTHIOPHENES - YET LONGER - SYNTHESIS, CHARACTERIZATION, AND SCANNING-TUNNELING-MICROSCOPY IMAGES OF HOMOLOGOUS, ISOMERICALLY PURE OLIGO(ALKYLTHIOPHENE)S [J].
BAUERLE, P ;
FISCHER, T ;
BIDLINGMEIER, B ;
STABEL, A ;
RABE, JP .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1995, 34 (03) :303-307
[4]  
Briehn CA, 2001, ANGEW CHEM INT EDIT, V40, P4680, DOI 10.1002/1521-3773(20011217)40:24<4680::AID-ANIE4680>3.0.CO
[5]  
2-X
[6]   SPHERANDS-LIGANDS WHOSE BINDING OF CATIONS RELIEVES ENFORCED ELECTRON-ELECTRON REPULSIONS [J].
CRAM, DJ ;
KANEDA, T ;
HELGESON, RC ;
LEIN, GM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1979, 101 (22) :6752-6754
[7]   Investigation of barriers to conformational interchange in oligothiophenes and oligo(thienyl)furans [J].
Diaz-Quijada, GA ;
Weinberg, N ;
Holdcroft, S ;
Pinto, BM .
JOURNAL OF PHYSICAL CHEMISTRY A, 2002, 106 (07) :1266-1276
[8]  
Diedrich F., 1998, Metal-Catalyzed Cross-Coupling Reactions
[9]   Building blocks for n-type organic electronics: Regiochemically modulated inversion of majority carrier sign in perfluoroarene-modified polythiophene semiconductors [J].
Facchetti, A ;
Yoon, MH ;
Stern, CL ;
Katz, HE ;
Marks, TJ .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (33) :3900-3903
[10]   High carrier mobility up to 0.1 cm2V-1s-1 at ambient temperatures in thiophene-based smectic liquid crystals [J].
Funahashi, M ;
Hanna, JI .
ADVANCED MATERIALS, 2005, 17 (05) :594-+