Synthesis of conjugated 2 and 2,5-(ethenyl) and (ethynyl)phenylethynyl thiophenes: fluorescence properties

被引:20
作者
Rodriguez, JG [1 ]
Esquivias, J [1 ]
Lafuente, A [1 ]
Rubio, L [1 ]
机构
[1] Univ Autonoma Madrid, Dept Quim Organ, E-28049 Madrid, Spain
关键词
arylethynylthiophenes; pi-extended conjugation; Eglinton-Glaser reactions; Cadiot-Chodkiewicz reaction; Sonogashira reaction; fluorescence;
D O I
10.1016/j.tet.2006.01.032
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Nano conjugated thienylethenyl and thienylethynyl Compounds with controlled Structure and dimensions have been efficiently prepared, by heterocoupling reaction between 1,4-(thienylethynylphenyl)phenylacetylene (or thienylethenyl)phenylacetylene and 2- or 2,5-dihalothiophene. Conjugated 1,4-di(2-thienylethynylphenyl)- (or 2-thienylethenylphenyl)-1,3-butadiyne were obtained by the homocoupling of the terminal acetylenes in excellent yield. The end-capped (N,N-dimethylaminophenyl)- and [3,5-di(trimethylsilylethynyl)-1-ethynyl]-2,5-di(iodo)thiophene were obtained by the heterocoupling between the corresponding terminal acetylene and 2,5-di(iodo)thiophene, catalyzed by the bis(triphenylphosphine)palladium and cuprous iodide system in excellent yield. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3112 / 3122
页数:11
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