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dc.contributor.authorKrinochkin, A. P.en
dc.contributor.authorValieva, M. I.en
dc.contributor.authorStarnovskaya, E. S.en
dc.contributor.authorShtaitz, Y. K.en
dc.contributor.authorKopchuk, D. S.en
dc.contributor.authorTaniya, O. S.en
dc.contributor.authorKim, G. A.en
dc.contributor.authorShevyrin, V. A.en
dc.contributor.authorZyryanov, G. V.en
dc.contributor.authorChupakhin, O. N.en
dc.date.accessioned2024-04-05T16:34:52Z-
dc.date.available2024-04-05T16:34:52Z-
dc.date.issued2023-
dc.identifier.citationKrinochkin, AP, Valieva, MI, Starnovskaya, ES, Shtaitz, YK, Kopchuk, DS, Taniya, OS, Kim, GA, Shevyrin, VA, Zyryanov, GV & Chupakhin, ON 2023, 'Comparison of Photophysical Properties of Lanthanide(III) Complexes of DTTA- or DO3A-Appended Aryl-2,2′-Bipyridines', Molecules, Том. 28, № 2, 724. https://doi.org/10.3390/molecules28020724harvard_pure
dc.identifier.citationKrinochkin, A. P., Valieva, M. I., Starnovskaya, E. S., Shtaitz, Y. K., Kopchuk, D. S., Taniya, O. S., Kim, G. A., Shevyrin, V. A., Zyryanov, G. V., & Chupakhin, O. N. (2023). Comparison of Photophysical Properties of Lanthanide(III) Complexes of DTTA- or DO3A-Appended Aryl-2,2′-Bipyridines. Molecules, 28(2), [724]. https://doi.org/10.3390/molecules28020724apa_pure
dc.identifier.issn1420-3049-
dc.identifier.otherFinal2
dc.identifier.otherAll Open Access, Gold, Green3
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85146686137&doi=10.3390%2fmolecules28020724&partnerID=40&md5=5b0a8b9521f2648bab799caa975a91171
dc.identifier.otherhttps://www.mdpi.com/1420-3049/28/2/724/pdf?version=1673482519pdf
dc.identifier.urihttp://elar.urfu.ru/handle/10995/130881-
dc.description.abstractNew Tb(III) and Eu(III) complexes based on aryl-2,2′-bipyridine ligands with a cyclic DO3A chelating unit appended in the alpha position of the bipyridine core were synthesized. The photophysical properties of these complexes were compared with those of complexes of ligands with identical aryl-2,2′-bipyridine chromophores, but with an acyclic DTTA residue as an additional chelating site in the alpha position of the bipyridine core. The nature of the polyaminocarboxylic acid fragments was found to have a significant influence on the luminescence. For some of the Eu(III) complexes, upon the transition from acyclic DTTA- to the cyclic DO3A-appended ligands, a noticeable increase in the intensity of Eu(III) luminescence was observed, with an increase in the quantum yield of up to 2.55 times. In contrast, for most of the Tb(III) complexes, a similar transition resulted in a noticeable decrease in the luminescence intensity of the Tb(III) cation. © 2023 by the authors.en
dc.description.sponsorshipMinistry of Science, ICT and Future Planning, MSIP: 075-15-2022-1118; Russian Science Foundation, RSF: 18-73-10119-Pen
dc.description.sponsorshipThis research was supported by the Russian Scientific Foundation: Ref. # 18-73-10119-P (the synthesis and investigation of DTTA-appended chelates) and Ministry of Science and the Higher Education of RF: Ref. # 075-15-2022-1118, dated 29 June 2022 (the synthesis and investigation of DO3A-appended chelates).en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherMDPIen
dc.relationinfo:eu-repo/grantAgreement/RSF//18-73-10119en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.rightscc-byother
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/unpaywall
dc.sourceMolecules2
dc.sourceMoleculesen
dc.subject2,2′-BIPYRIDINESen
dc.subjectCOMPARISON OF PHOTOPHYSICAL PROPERTIESen
dc.subjectDO3Aen
dc.subjectDTTAen
dc.subjectEU(III) COMPLEXen
dc.subjectLANTHANIDE(III) CATION LUMINESCENCEen
dc.subjectTB(III) COMPLEXen
dc.titleComparison of Photophysical Properties of Lanthanide(III) Complexes of DTTA- or DO3A-Appended Aryl-2,2′-Bipyridinesen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.type|info:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.3390/molecules28020724-
dc.identifier.scopus85146686137-
local.contributor.employeeKrinochkin, A.P., 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.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.employeeShtaitz, Y.K., Chemical Engineering Institute, Ural Federal University, 19 Mira St., Yekaterinburg, 620002, 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.employeeTaniya, O.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.employeeKim, G.A., 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.employeeShevyrin, V.A., Chemical Engineering Institute, Ural Federal University, 19 Mira St., Yekaterinburg, 620002, 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.issue2-
local.volume28-
dc.identifier.wos000931403900001-
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.identifier.pure33981311-
local.description.order724-
local.identifier.eid2-s2.0-85146686137-
local.fund.rsf18-73-10119-
local.identifier.wosWOS:000931403900001-
local.identifier.pmid36677784-
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