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Selective thienylation of fluorinated benzothiadiazoles and benzotriazoles for organic photovoltaics
Alternative Title氟代苯丙噻二唑和三氮唑的选择性噻吩化
He CY(贺春阳)1; Wu CZ(吴才智)1; Zhu YL(朱炎麟)1; Zhang XG(张新刚)1
2014
Source PublicationChem. Sci.
Volume5Issue:4Pages:1317-1321
AbstractAn unprecedented example for the selective and efficient synthesis of an FBT-thiophene structural motif via dual C-H functionalization, catalyzed by palladium, has been developed. Fluorinated benzotriazole is also applicable to the reaction. This protocol provides facile access to unsymmetrical and symmetrical thienylated FBTs that can be applied in the development of high performance photovoltaics, in particular in bulk heterojunction (BHJ) solar cells.
Subject Area氟化学
DOI10.1039/c3sc53119h
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Indexed BySCI
Language英语
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Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/38878
Collection中科院有机氟化学重点实验室
Corresponding AuthorZhang XG(张新刚)
Affiliation1.中科院上海有机化学研究所
2.东华大学
Recommended Citation
GB/T 7714
He CY,Wu CZ,Zhu YL,et al. Selective thienylation of fluorinated benzothiadiazoles and benzotriazoles for organic photovoltaics[J]. Chem. Sci.,2014,5(4):1317-1321.
APA 贺春阳,吴才智,朱炎麟,&张新刚.(2014).Selective thienylation of fluorinated benzothiadiazoles and benzotriazoles for organic photovoltaics.Chem. Sci.,5(4),1317-1321.
MLA 贺春阳,et al."Selective thienylation of fluorinated benzothiadiazoles and benzotriazoles for organic photovoltaics".Chem. Sci. 5.4(2014):1317-1321.
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