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dc.contributor.authorKrinochkin, A. P.en
dc.contributor.authorKopchuk, D. S.en
dc.contributor.authorKhasanov, A. F.en
dc.contributor.authorChepchugov, N. V.en
dc.contributor.authorKovalev, I. S.en
dc.contributor.authorSantra, S.en
dc.contributor.authorZyryanov, G. V.en
dc.contributor.authorMajee, A.en
dc.contributor.authorRusinov, V. L.en
dc.contributor.authorChupakhin, O. N.en
dc.date.accessioned2022-05-12T08:21:13Z-
dc.date.available2022-05-12T08:21:13Z-
dc.date.issued2017-
dc.identifier.citationUnsymmetrically Functionalized 5,5″-diaryl-and 5,6,5″-triaryl-2,2′:6′,2″-terpyridines: An Efficient Synthetic Route and Photophysical Properties / A. P. Krinochkin, D. S. Kopchuk, A. F. Khasanov et al. // Canadian Journal of Chemistry. — 2017. — Vol. 95. — Iss. 8. — P. 851-857.en
dc.identifier.issn0008-4042-
dc.identifier.otherAll Open Access, Green3
dc.identifier.urihttp://elar.urfu.ru/handle/10995/111719-
dc.description.abstractAn efficient approach for the synthesis of 5,5″-or 5,6,5″-aryl substituted 2,2′:6′,2″-terpyridines, bearing an anneleted cyclopentene unit in one of the side-chain pyridine rings for the improved solubility in organic solvents, via their 1,2,4-triazine analogues has been developed. By using this approach, various aromatic substituents were introduced in the 2,2′:6′,2″-terpyridine core. Depending on the nature of the aromatic substituents, the obtained terpyridines exhibited an intense emission in a range of ca. 344-394 nm in acetonitrile solutions. For the most representative compounds, pronounced bathochromic shifts in both absorption and emission spectra were observed compared with previously reported substituted terpyridines. © 2017 Published by NRC Research Press.en
dc.description.sponsorshipThis work was supported by the Russian Science Foundation (grant No. 15-13-10033), as well as the Council for grants of the President of the Russian Federation (to D.S. Kopchuk; grant No. MK-644.2017.3).en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherCanadian Science Publishingen1
dc.publisherCanadian Science Publishingen
dc.relationinfo:eu-repo/grantAgreement/RSF//15-13-10033en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.sourceCan. J. Chem.2
dc.sourceCanadian Journal of Chemistryen
dc.subject1 2 4-TRIAZINESen
dc.subject2 2′:6′ 2″-TERPYRIDINESen
dc.subjectAZA-DIELS-ALDER REACTIONen
dc.subjectFLUORESCENCEen
dc.subjectAROMATIC COMPOUNDSen
dc.subjectEMISSION SPECTROSCOPYen
dc.subjectFLUORESCENCEen
dc.subject1 2 4-TRIAZINESen
dc.subjectABSORPTION AND EMISSION SPECTRAen
dc.subjectACETONITRILE SOLUTIONSen
dc.subjectBATHOCHROMIC SHIFTen
dc.subjectDIELS-ALDER REACTIONen
dc.subjectPHOTOPHYSICAL PROPERTIESen
dc.subjectREPRESENTATIVE COMPOUNDen
dc.subjectTERPYRIDINESen
dc.subjectSYNTHESIS (CHEMICAL)en
dc.titleUnsymmetrically Functionalized 5,5″-diaryl-and 5,6,5″-triaryl-2,2′:6′,2″-terpyridines: An Efficient Synthetic Route and Photophysical Propertiesen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeinfo:eu-repo/semantics/acceptedVersionen
dc.identifier.doi10.1139/cjc-2017-0195-
dc.identifier.scopus85026846599-
local.contributor.employeeKrinochkin, A.P., Ural Federal University, 19, Mira St., Yekaterinburg, 62000, Russian Federation; Kopchuk, D.S., Ural Federal University, 19, Mira St., Yekaterinburg, 62000, Russian Federation, I. Ya. Postovsky Institute of Organic Synthesis of RAS (Ural Division), 22/20, S. Kovalevskoy/Akademicheskaya St., Yekaterinburg, 62099, Russian Federation; Khasanov, A.F., Ural Federal University, 19, Mira St., Yekaterinburg, 62000, Russian Federation; Chepchugov, N.V., Ural Federal University, 19, Mira St., Yekaterinburg, 62000, Russian Federation; Kovalev, I.S., Ural Federal University, 19, Mira St., Yekaterinburg, 62000, Russian Federation; Santra, S., Ural Federal University, 19, Mira St., Yekaterinburg, 62000, Russian Federation; Zyryanov, G.V., Ural Federal University, 19, Mira St., Yekaterinburg, 62000, Russian Federation, I. Ya. Postovsky Institute of Organic Synthesis of RAS (Ural Division), 22/20, S. Kovalevskoy/Akademicheskaya St., Yekaterinburg, 62099, Russian Federation; Majee, A., Department of Chemistry, Visva-Bharati (A Central University), Santiniketan, 731235, India; Rusinov, V.L., Ural Federal University, 19, Mira St., Yekaterinburg, 62000, Russian Federation, I. Ya. Postovsky Institute of Organic Synthesis of RAS (Ural Division), 22/20, S. Kovalevskoy/Akademicheskaya St., Yekaterinburg, 62099, Russian Federation; Chupakhin, O.N., Ural Federal University, 19, Mira St., Yekaterinburg, 62000, Russian Federation, I. Ya. Postovsky Institute of Organic Synthesis of RAS (Ural Division), 22/20, S. Kovalevskoy/Akademicheskaya St., Yekaterinburg, 62099, Russian Federationen
local.description.firstpage851-
local.description.lastpage857-
local.issue8-
local.volume95-
dc.identifier.wos000406998100007-
local.contributor.departmentUral Federal University, 19, Mira St., Yekaterinburg, 62000, Russian Federation; I. Ya. Postovsky Institute of Organic Synthesis of RAS (Ural Division), 22/20, S. Kovalevskoy/Akademicheskaya St., Yekaterinburg, 62099, Russian Federation; Department of Chemistry, Visva-Bharati (A Central University), Santiniketan, 731235, Indiaen
local.identifier.pure1969513-
local.identifier.eid2-s2.0-85026846599-
local.fund.rsf15-13-10033-
local.identifier.wosWOS:000406998100007-
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