著者
Karin Nakamura Shunsuke Tamba Atsushi Sugie Atsunori Mori
出版者
(社)日本化学会
雑誌
Chemistry Letters (ISSN:03667022)
巻号頁・発行日
pp.130523, (Released:2013-06-29)
被引用文献数
9

Thiophene based block copolymers are synthesized by addition of bromothiophene and Knochel-Hauser base (TMPMgCl·LiCl). Nickel-catalyzed deprotonative C–H coupling polycondensation of 3-substituted-thiophenes proceeds to give head-to-tail-type poly(3-substituted thiophen-2,5-diyl) bearing nickel at the polymer end. Block copolymers of thiophene derivatives are obtained by successive addition of 2-bromo-3-alkylthiophene and magnesium amide to a living polythiophene end. The use of nickel catalyst bearing an o-tolyl group gives the tolyl-group-terminated thiophene diblock copolymers in highly efficiently. Triblock copolymer is also synthesized by the iterative addition of bromothiophene and TMPMgCl·LiCl.
著者
Karin Nakamura Shunsuke Tamba Atsushi Sugie Atsunori Mori
出版者
(社)日本化学会
雑誌
Chemistry Letters (ISSN:03667022)
巻号頁・発行日
vol.42, no.10, pp.1200-1202, 2013-10-05 (Released:2013-10-05)
参考文献数
38
被引用文献数
9

Thiophene-based block copolymers are synthesized by addition of bromothiophene and the Knochel–Hauser base (TMPMgCl·LiCl). Nickel-catalyzed deprotonative C–H coupling polycondensation of 3-substituted-thiophenes proceeds to give head-to-tail-type poly(3-substituted thiophen-2,5-diyl) bearing nickel at the polymer end. Block copolymers of thiophene derivatives are obtained by successive addition of 2-bromo-3-alkylthiophene and magnesium amide to a living polythiophene end. The use of nickel catalyst bearing an o-tolyl group gives the tolyl-group-terminated thiophene diblock copolymers in high efficiency. Triblock copolymer is also synthesized by the iterative addition of bromothiophene and TMPMgCl·LiCl.