Electroactive D-A derivatives bearing 2,3-dimethylindole and tetrafluorostyrene moieties: Synthesis, polymerization, DFT calculations and photophysical properties

Two electroactive compounds, bearing 2,3-dimethylindole donor moiety and tetrafluorostyrene acceptor moiety, were designed and synthesized by employing one-step nucleophilic aromatic substitution reaction. Radical polymerization was used to obain electroactive linear polymer. Their photophysical pro...

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Bibliographic Details
Published inMolecular crystals and liquid crystals (Philadelphia, Pa. : 2003) Vol. 671; no. 1; pp. 24 - 32
Main Authors Eltan, T., Lapienyte, L., Keruckiene, R., Leitonas, K., Simokaitiene, J., Buika, G., Grazulevicius, J. V.
Format Journal Article
LanguageEnglish
Published Taylor & Francis 13.08.2018
Subjects
2,3-dimethylindole
electroactive
ionization potential
tetrafluorostyrene
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Summary:Two electroactive compounds, bearing 2,3-dimethylindole donor moiety and tetrafluorostyrene acceptor moiety, were designed and synthesized by employing one-step nucleophilic aromatic substitution reaction. Radical polymerization was used to obain electroactive linear polymer. Their photophysical properties, based on theoretical calculations and experimental measurements, as well as electrochemical and photoelectrical properties are discussed.
ISSN:1542-1406
1563-5287
DOI:10.1080/15421406.2018.1542082