Polyfluorinated triphenyl-4,5-dihydro-1H-pyrazoles with dendroid arylsulfanyl moieties as donor blocks in donor-acceptor chromophores Научная публикация
Журнал |
Journal of Fluorine Chemistry
ISSN: 0022-1139 |
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Вых. Данные | Год: 2021, Том: 248, Номер статьи : 109841, Страниц : DOI: 10.1016/j.jfluchem.2021.109841 | ||||||||
Ключевые слова | Dendroid moieties; DFT calculations; Donor-acceptor chromophores; Polyfluorinated pyrazolines; UV/Vis-spectra | ||||||||
Авторы |
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Организации |
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Реферат:
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
Библиографическая ссылка:
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
Идентификаторы:
Web of science | WOS:000675502700013 |
Scopus | 2-s2.0-85110104516 |
РИНЦ | 46892366 |
OpenAlex | W3182648517 |