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Formal preparation of regioregular and alternating thiophene–thiophene copolymers bearing different substituents

Differently substituted thiophene–thiophene-alternating copolymers were formally synthesized employing a halo-bithiophene as a monomer. Nickel-catalyzed polymerization of bithiophene with substituents at the 3-position, including alkyl-, fluoroalkyl-, or oligosiloxane-containing groups, afforded the...

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Detalles Bibliográficos
Autores principales: Mori, Atsunori, Fujita, Keisuke, Kubota, Chihiro, Suzuki, Toyoko, Okano, Kentaro, Matsumoto, Takuya, Nishino, Takashi, Horie, Masaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082695/
https://www.ncbi.nlm.nih.gov/pubmed/32256849
http://dx.doi.org/10.3762/bjoc.16.31
Descripción
Sumario:Differently substituted thiophene–thiophene-alternating copolymers were formally synthesized employing a halo-bithiophene as a monomer. Nickel-catalyzed polymerization of bithiophene with substituents at the 3-position, including alkyl-, fluoroalkyl-, or oligosiloxane-containing groups, afforded the corresponding copolymers in good to excellent yield. The solubility test in organic solvents was performed to reveal that several copolymers showed a superior solubility. X-ray diffraction analysis of the thin film of the alternating copolymers composed of methyl and branched oligosiloxane substituents was also performed, and the results suggested the formation of a dual-layered film structure.