EFFICIENT PALLADIUM-CATALYZED SYNTHESIS OF UNSYMMETRICAL DONOR-ACCEPTOR BIARYLS AND POLYARYLS

被引:50
作者
AMATORE, C
JUTAND, A
NEGRI, S
FAUVARQUE, JF
机构
[1] ECOLE NORM SUPER, CHIM LAB, CNRS, UNITE 1110, 24 RUE LHOMOND, F-75231 PARIS 05, FRANCE
[2] LAB MARCOUSSIS, F-91460 MARCOUSSIS, FRANCE
关键词
D O I
10.1016/0022-328X(90)85107-A
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
4,4′-Unsymmetrically substituted biphenyls can be synthesized by cross-coupling reactions of substituted aromatic organometallic reagents and aromatic halides catalyzed by palladium complexes. This two-step method from commercially available aromatic halides has been used for the synthesis of a series of donor/acceptor para-substituted biphenyls, DC6H4C6H4A, where D is an electron donor group and A an electron acceptor group, which are of interest as liquid crystal precursors and as having potential in non-linear optics. Biaryls in which the donor-phenyl moiety is replaced by a 2-furyl or 2-thienyl can be synthesized similarly. The method can also be used for the convergent synthesis of previously unreported unsymmetrically substituted polyparaphenylenes {A figure is presented} (n = 3,4). © 1990.
引用
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页码:389 / 398
页数:10
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