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http://elar.urfu.ru/handle/10995/131322
Название: | Synthesis and Photophysical Properties of α-(N-Biphenyl)-Substituted 2,2′-Bipyridine-Based Push–Pull Fluorophores |
Авторы: | Starnovskaya, E. S. Kopchuk, D. S. Khasanov, A. F. Taniya, O. S. Nikonov, I. L. Valieva, M. I. Pavlyuk, D. E. Novikov, A. S. Zyryanov, G. V. Chupakhin, O. N. |
Дата публикации: | 2022 |
Издатель: | MDPI |
Библиографическое описание: | Starnovskaya, ES, Kopchuk, DS, Khasanov, AF, Taniya, OS, Nikonov, IL, Valieva, MI, Pavlyuk, DE, Novikov, AS, Zyryanov, GV & Chupakhin, ON 2022, 'Synthesis and Photophysical Properties of α-(N-Biphenyl)-Substituted 2,2′-Bipyridine-Based Push–Pull Fluorophores', Molecules, Том. 27, № 20, 6879. https://doi.org/10.3390/molecules27206879 Starnovskaya, E. S., Kopchuk, D. S., Khasanov, A. F., Taniya, O. S., Nikonov, I. L., Valieva, M. I., Pavlyuk, D. E., Novikov, A. S., Zyryanov, G. V., & Chupakhin, O. N. (2022). Synthesis and Photophysical Properties of α-(N-Biphenyl)-Substituted 2,2′-Bipyridine-Based Push–Pull Fluorophores. Molecules, 27(20), [6879]. https://doi.org/10.3390/molecules27206879 |
Аннотация: | A series of new α-(N-biphenyl)-substituted 2,2′-bipyridines were obtained through the combination of the ipso-nucleophilic aromatic substitution of the C5-cyano group, aza-Diels–Alder and Suzuki cross-coupling reactions, starting from 5-cyano-1,2,4-triazines. For the obtained compounds, photophysical and fluorosolvatochromic properties were studied. Fluorophores 3l and 3b demonstrated unexpected AIEE activity, while 3a and 3h showed promising nitroexplosive detection abilities. © 2022 by the authors. |
Ключевые слова: | AIEE FLUORESCENCE FLUOROSOLVATOCHROMIC PROPERTIES HAMMETT CONSTANTS LIPPERT–MATAGA EQUATION NITROEXPLOSIVE DETECTION Α-(N-BIPHENYL)-SUBSTITUTED 2,2′-BIPYRIDINES “PUSH–PULL” FLUOROPHORES 2,2'-DIPYRIDYL BIPHENYL COMPOUNDS FLUORESCENT DYES IONOPHORES TRIAZINES 2,2' BIPYRIDINE BIPHENYL BIPHENYL DERIVATIVE FLUORESCENT DYE IONOPHORE TRIAZINE DERIVATIVE |
URI: | http://elar.urfu.ru/handle/10995/131322 |
Условия доступа: | info:eu-repo/semantics/openAccess cc-by |
Текст лицензии: | https://creativecommons.org/licenses/by/4.0/ |
Идентификатор SCOPUS: | 85140873129 |
Идентификатор WOS: | 000872811600001 |
Идентификатор PURE: | 31570847 e815c794-b10c-4789-8945-25ba94eee220 |
ISSN: | 1420-3049 |
DOI: | 10.3390/molecules27206879 |
Сведения о поддержке: | Russian Science Foundation, RSF, (21-13-00304) Council on grants of the President of the Russian Federation, (075-15-2022-802, NSh- 1223.2022.1.3) RUDN University This research was funded by the Russian Scientific Foundation, grant number 19-73-10144-P dated 2 August 2022 (Photophysical Studies and Studies of Fluorosolvatochromism) and 21-13-00304 dated 19 April 2021 (AIEE Studies)), by the Grants Council of the President of the Russian Federation (grant number NSh- 1223.2022.1.3, state contract № 075-15-2022-802 dated 6 May 2022) and the RUDN University Strategic Academic Leadership Program. |
Карточка проекта РНФ: | 21-13-00304 |
Располагается в коллекциях: | Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC |
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2-s2.0-85140873129.pdf | 4,89 MB | Adobe PDF | Просмотреть/Открыть |
Лицензия на ресурс: Лицензия Creative Commons