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Название: Push–Pull Derivatives Based on 2,4′-Biphenylene Linker with Quinoxaline, [1,2,5]Oxadiazolo[3,4-B]Pyrazine and [1,2,5]Thiadiazolo[3,4-B]Pyrazine Electron Withdrawing Parts
Авторы: Verbitskiy, E. V.
Le Poul, P.
Bureš, F.
Achelle, S.
Barsella, A.
Kvashnin, Y. A.
Rusinov, G. L.
Charushin, V. N.
Дата публикации: 2022
Библиографическое описание: Push–Pull Derivatives Based on 2,4′-Biphenylene Linker with Quinoxaline, [1,2,5]Oxadiazolo[3,4-B]Pyrazine and [1,2,5]Thiadiazolo[3,4-B]Pyrazine Electron Withdrawing Parts / E. V. Verbitskiy, P. Le Poul, F. Bureš et al. // Molecules. — 2022. — Vol. 27. — Iss. 13. — 4250.
Аннотация: A series of novel V-shaped quinoxaline, [1,2,5]oxadiazolo[3,4-b]pyrazine and [1,2,5]thia-diazolo[3,4-b]pyrazine push–pull derivatives with 2,4′-biphenylene linker were designed and their electrochemical, photophysical and nonlinear optical properties were investigated. [1,2,5]Oxadia-zolo[3,4-b]pyrazine is the stronger electron-withdrawing fragment as shown by electrochemical, and photophysical data. All compounds are emissive in a solid-state (from the cyan to red region of the spectrum) and quinoxaline derivatives are emissions in DCM solution. It has been found that quinoxaline derivatives demonstrate important solvatochromism and extra-large Stokes shifts, characteristic of twisted intramolecular charge transfer excited state as well as aggregation induced emission. The experimental conclusions have been justified by theoretical (TD-)DFT calculations. © 2022 by the authors. Li-censee MDPI, Basel, Switzerland.
Ключевые слова: DONOR–ACCEPTOR SYSTEMS
FURAZANOPYRAZINE
QUINOXALINE
TWISTED INTRAMOLECULAR CHARGE TRANSFER
[1,2,5]THIADIAZOLO[3,4-B]PYRAZINE
URI: http://elar.urfu.ru/handle/10995/117960
Условия доступа: info:eu-repo/semantics/openAccess
Идентификатор SCOPUS: 85133415309
Идентификатор WOS: 000823933800001
Идентификатор PURE: 30531362
DOI: 10.3390/molecules27134250
Сведения о поддержке: Grantová Agentura České Republiky, GA ČR: 22-14988S; Russian Science Foundation, RSF: 19-13-00234
Funding: This research was funded by Russian Science Foundation, grant number No. 19-13-00234. F.B. is indebted to the Czech Science Foundation (22-14988S)
This research was funded by Russian Science Foundation, grant number No. 19-13-00234. F.B. is indebted to the Czech Science Foundation (22-14988S).
Карточка проекта РНФ: 19-13-00234
Располагается в коллекциях:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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