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Donor-acceptor copolymers with 1,7-regioisomers of N,N′-dialkylperylene-3,4,9,10-tetracarboxydiimide as materials for photonics

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    SYSNO ASEP0512150
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleDonor-acceptor copolymers with 1,7-regioisomers of N,N′-dialkylperylene-3,4,9,10-tetracarboxydiimide as materials for photonics
    Author(s) Cimrová, Věra (UMCH-V) RID, ORCID
    Výprachtický, Drahomír (UMCH-V) RID, ORCID
    Pokorná, Veronika (UMCH-V) RID
    Babičová, Petra (UMCH-V) RID
    Source TitleJournal of Materials Chemistry C. - : Royal Society of Chemistry - ISSN 2050-7526
    Roč. 7, č. 46 (2019), s. 14678-14692
    Number of pages15 s.
    Languageeng - English
    CountryGB - United Kingdom
    Keywordsdonor-acceptor copolymers ; perylenetetracarboxydiimide acceptor units ; synthesis
    Subject RIVCD - Macromolecular Chemistry
    OECD categoryPolymer science
    R&D ProjectsGC18-14683J GA ČR - Czech Science Foundation (CSF)
    Method of publishingLimited access
    Institutional supportUMCH-V - RVO:61389013
    UT WOS000506638900027
    EID SCOPUS85075826442
    DOI10.1039/C9TC05233J
    AnnotationDonor–acceptor (D–A) copolymers containing N,N′-dialkylperylene-3,4,9,10-tetracarboxydiimide electron-acceptor units with dodecyl (DDPDI) or 2-ethylhexyl (EHPDI) substituents and three different electron-donor units (9,9-dioctylfluorene, 9-(2-ethylhexyl)carbazole or 9-(heptadecan-9-yl)carbazole) were synthesized by Suzuki coupling and were then characterized. Their thermal, photophysical, electrochemical and spectroelectrochemical properties were studied. The effects of the alkyl side chain combination on the properties were evaluated and are discussed. Despite large differences in the absorption spectra of the individual DDPDI and EHPDI units or monomers in solutions and thin films, the absorption spectra of the copolymers in solutions and thin films exhibited similar shapes. More pronounced side chain effects were observed in the photoluminescent (PL) behaviour than in the absorption behaviour. Different alkyl side chains on the D–A copolymers similarly affected the visible absorption band contributions in the solutions and thin films, but the exhibited effects were different for the PL spectra and efficiency. The copolymers exhibited reversible reduction and irreversible oxidation. The ionization potential and bandgap values were influenced by the donor unit and by the perylene-3,4,9,10-tetracarboxydiimide (PDI) side chain nature. Spectroelectrochemical changes are reported, and potential sensing applications are outlined.
    WorkplaceInstitute of Macromolecular Chemistry
    ContactEva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358
    Year of Publishing2020
    Electronic addresshttps://pubs.rsc.org/en/content/articlelanding/2019/TC/C9TC05233J#!divAbstract
Number of the records: 1  

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