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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
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 Ishchenko Roman A. 1,2 , Kargapolova Irina Yu. 1 , Orlova Natalia А. 1 , Shelkovnikov Vladimir V. 1,3 , Maksimov Alexander М. 1 , Ryazanov Nikita D. 1,2 , Berezhnaya Viktoria N. 1,2 , Chernonosov Alexander А. 4
Организации
1 N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry of the Siberian Branch of Russian Academy of Sciences, 9 Academician Lavrentjev Ave., Novosibirsk, 630090, Russian Federation
2 Novosibirsk State University, Pirogov Street 1, Novosibirsk, 630090, Russian Federation
3 Novosibirsk State Technical University, Karl Marx Prospect 20, Novosibirsk, 630073, Russian Federation
4 Institute of Chemical Biology and Fundamental Medicine, Siberian Branch, Russian Academy of Sciences, Academician Lavrent′ev Prospect 8, Novosibirsk, 630090, Russian Federation

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 OpenAlex
Идентификаторы БД:
Web of science: WOS:000675502700013
Scopus: 2-s2.0-85110104516
РИНЦ: 46892366
OpenAlex: W3182648517
Цитирование в БД:
БД Цитирований
Scopus 4
Web of science 7
РИНЦ 2
OpenAlex 5
Альметрики: