Polyfluorinated triphenyl-4,5-dihydro-1H-pyrazoles with dendroid arylsulfanyl moieties as donor blocks in donor-acceptor chromophores Full article
Journal |
Journal of Fluorine Chemistry
ISSN: 0022-1139 |
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Output data | Year: 2021, Volume: 248, Article number : 109841, Pages count : DOI: 10.1016/j.jfluchem.2021.109841 | ||||||||
Tags | Dendroid moieties; DFT calculations; Donor-acceptor chromophores; Polyfluorinated pyrazolines; UV/Vis-spectra | ||||||||
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Abstract:
A series of novel donor-acceptor chromophores were synthesized using formylated derivatives of polyfluorinated triarylpyrazolines with branched moieties as donor blocks and dicyanoisophorone as acceptor. The nucleophilic substitution of fluorine with 4-hydroxypiperidine in decafluoropyrazoline was used to further functionalize the chromophore molecule. An existing method for introducing the dendroid moiety was improved. The properties of the final chromophores were estimated by DFT calculations. © 2021
Cite:
Ishchenko R.A.
, Kargapolova I.Y.
, Orlova N.А.
, Shelkovnikov V.V.
, Maksimov A.М.
, Ryazanov N.D.
, Berezhnaya V.N.
, Chernonosov A.А.
Polyfluorinated triphenyl-4,5-dihydro-1H-pyrazoles with dendroid arylsulfanyl moieties as donor blocks in donor-acceptor chromophores
Journal of Fluorine Chemistry. 2021. V.248. 109841 . DOI: 10.1016/j.jfluchem.2021.109841 WOS Scopus РИНЦ
Polyfluorinated triphenyl-4,5-dihydro-1H-pyrazoles with dendroid arylsulfanyl moieties as donor blocks in donor-acceptor chromophores
Journal of Fluorine Chemistry. 2021. V.248. 109841 . DOI: 10.1016/j.jfluchem.2021.109841 WOS Scopus РИНЦ
Identifiers:
Web of science | WOS:000675502700013 |
Scopus | 2-s2.0-85110104516 |
Elibrary | 46892366 |
OpenAlex | W3182648517 |