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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… Click to show full abstract
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.
Journal Title: Chemical communications
Year Published: 2022
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