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  3. Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC
Please use this identifier to cite or link to this item: http://elar.urfu.ru/handle/10995/131322
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dc.contributor.authorStarnovskaya, E. S.en
dc.contributor.authorKopchuk, D. S.en
dc.contributor.authorKhasanov, A. F.en
dc.contributor.authorTaniya, O. S.en
dc.contributor.authorNikonov, I. L.en
dc.contributor.authorValieva, M. I.en
dc.contributor.authorPavlyuk, D. E.en
dc.contributor.authorNovikov, A. S.en
dc.contributor.authorZyryanov, G. V.en
dc.contributor.authorChupakhin, O. N.en
dc.date.accessioned2024-04-08T11:06:37Z-
dc.date.available2024-04-08T11:06:37Z-
dc.date.issued2022-
dc.identifier.citationStarnovskaya, 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/molecules27206879harvard_pure
dc.identifier.citationStarnovskaya, 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/molecules27206879apa_pure
dc.identifier.issn1420-3049-
dc.identifier.otherFinal2
dc.identifier.otherAll Open Access; Gold Open Access; Green Open Access3
dc.identifier.otherhttps://www.mdpi.com/1420-3049/27/20/6879/pdf?version=16666844601
dc.identifier.otherhttps://www.mdpi.com/1420-3049/27/20/6879/pdf?version=1666684460pdf
dc.identifier.urihttp://elar.urfu.ru/handle/10995/131322-
dc.description.abstractA 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.en
dc.description.sponsorshipRussian Science Foundation, RSF, (21-13-00304)en
dc.description.sponsorshipCouncil on grants of the President of the Russian Federation, (075-15-2022-802, NSh- 1223.2022.1.3)en
dc.description.sponsorshipRUDN Universityen
dc.description.sponsorshipThis 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.en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherMDPIen
dc.relationinfo:eu-repo/grantAgreement/RSF//21-13-00304en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.rightscc-byother
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/unpaywall
dc.sourceMolecules2
dc.sourceMoleculesen
dc.subjectAIEEen
dc.subjectFLUORESCENCEen
dc.subjectFLUOROSOLVATOCHROMIC PROPERTIESen
dc.subjectHAMMETT CONSTANTSen
dc.subjectLIPPERT–MATAGA EQUATIONen
dc.subjectNITROEXPLOSIVE DETECTIONen
dc.subjectΑ-(N-BIPHENYL)-SUBSTITUTED 2,2′-BIPYRIDINESen
dc.subject“PUSH–PULL” FLUOROPHORESen
dc.subject2,2'-DIPYRIDYLen
dc.subjectBIPHENYL COMPOUNDSen
dc.subjectFLUORESCENT DYESen
dc.subjectIONOPHORESen
dc.subjectTRIAZINESen
dc.subject2,2' BIPYRIDINEen
dc.subjectBIPHENYLen
dc.subjectBIPHENYL DERIVATIVEen
dc.subjectFLUORESCENT DYEen
dc.subjectIONOPHOREen
dc.subjectTRIAZINE DERIVATIVEen
dc.titleSynthesis and Photophysical Properties of α-(N-Biphenyl)-Substituted 2,2′-Bipyridine-Based Push–Pull Fluorophoresen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.3390/molecules27206879-
dc.identifier.scopus85140873129-
local.contributor.employeeStarnovskaya E.S., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federation, I. Ya. Postovsky Institute of Organic Synthesis of RAS, Ural Division, 22/20 S. Kovalevskoy/Akademicheskaya St, Yekaterinburg, 62099, Russian Federationen
local.contributor.employeeKopchuk D.S., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federation, I. Ya. Postovsky Institute of Organic Synthesis of RAS, Ural Division, 22/20 S. Kovalevskoy/Akademicheskaya St, Yekaterinburg, 62099, Russian Federationen
local.contributor.employeeKhasanov A.F., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federationen
local.contributor.employeeTaniya O.S., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federationen
local.contributor.employeeNikonov I.L., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federation, I. Ya. Postovsky Institute of Organic Synthesis of RAS, Ural Division, 22/20 S. Kovalevskoy/Akademicheskaya St, Yekaterinburg, 62099, Russian Federationen
local.contributor.employeeValieva M.I., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federation, I. Ya. Postovsky Institute of Organic Synthesis of RAS, Ural Division, 22/20 S. Kovalevskoy/Akademicheskaya St, Yekaterinburg, 62099, Russian Federationen
local.contributor.employeePavlyuk D.E., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federationen
local.contributor.employeeNovikov A.S., Institute of Chemistry, Saint Petersburg State University, 7/9 Universitetskaya Nab, Saint Petersburg, 199034, Russian Federation, Research Institute of Chemistry, Peoples’ Friendship, University of Russia, RUDN University, 6 Miklukho-Maklaya St, Moscow, 117198, Russian Federationen
local.contributor.employeeZyryanov G.V., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federation, I. Ya. Postovsky Institute of Organic Synthesis of RAS, Ural Division, 22/20 S. Kovalevskoy/Akademicheskaya St, Yekaterinburg, 62099, Russian Federationen
local.contributor.employeeChupakhin O.N., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federation, I. Ya. Postovsky Institute of Organic Synthesis of RAS, Ural Division, 22/20 S. Kovalevskoy/Akademicheskaya St, Yekaterinburg, 62099, Russian Federationen
local.issue20-
local.volume27-
dc.identifier.wos000872811600001-
local.contributor.departmentChemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federationen
local.contributor.departmentI. Ya. Postovsky Institute of Organic Synthesis of RAS, Ural Division, 22/20 S. Kovalevskoy/Akademicheskaya St, Yekaterinburg, 62099, Russian Federationen
local.contributor.departmentInstitute of Chemistry, Saint Petersburg State University, 7/9 Universitetskaya Nab, Saint Petersburg, 199034, Russian Federationen
local.contributor.departmentResearch Institute of Chemistry, Peoples’ Friendship, University of Russia, RUDN University, 6 Miklukho-Maklaya St, Moscow, 117198, Russian Federationen
local.identifier.pure31570847-
local.identifier.puree815c794-b10c-4789-8945-25ba94eee220uuid
local.description.order6879-
local.identifier.eid2-s2.0-85140873129-
local.fund.rsf21-13-00304-
local.identifier.wosWOS:000872811600001-
local.identifier.pmid36296472-
Appears in Collections:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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