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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
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
Authors 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
Affiliations
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

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 OpenAlex
Identifiers:
Web of science: WOS:000675502700013
Scopus: 2-s2.0-85110104516
Elibrary: 46892366
OpenAlex: W3182648517
Citing:
DB Citing
Scopus 4
Web of science 7
Elibrary 2
OpenAlex 5
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