Synthesis and optoelectronic properties of radical conjugated polyfluorenes

A novel redox-active fluorene monomer is synthesized and copolymerized with 9,9-dioctylfluorene and benzo[ c ][1,2,5]thiadiazole via Suzuki cross-coupling to produce alternating and tertiary copolymers. Electrochemical and chemical reduction of the copolymers generates organic polymeric radical anio...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2022-08, Vol.58 (62), p.863-8633
Hauptverfasser: Cheng, Susan, Battaglia, Alicia M, Imperiale, Christian J, Lough, Alan, Wilson, Mark W. B, Seferos, Dwight S
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container_end_page 8633
container_issue 62
container_start_page 863
container_title Chemical communications (Cambridge, England)
container_volume 58
creator Cheng, Susan
Battaglia, Alicia M
Imperiale, Christian J
Lough, Alan
Wilson, Mark W. B
Seferos, Dwight S
description A novel redox-active fluorene monomer is synthesized and copolymerized with 9,9-dioctylfluorene and benzo[ c ][1,2,5]thiadiazole via Suzuki cross-coupling to produce alternating and tertiary copolymers. Electrochemical and chemical reduction of the copolymers generates organic polymeric radical anions. Electrochemical, spectroscopic, and photophysical characterization grant insight into the structure-property relationship for open-shell conjugated polymers. A novel redox-active fluorene monomer is synthesized and copolymerized with 9,9-dioctylfluorene and benzo[ c ][1,2,5]thiadiazole via Suzuki cross-coupling to produce alternating and tertiary copolymers.
doi_str_mv 10.1039/d2cc02406c
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source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Chemical reduction
Copolymerization
Copolymers
Cross coupling
Optoelectronics
Thiadiazoles
title Synthesis and optoelectronic properties of radical conjugated polyfluorenes
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