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dc.contributor.authorAlcolea, Palafox, M.en
dc.contributor.authorBelskaya, N. P.en
dc.contributor.authorTodorov, L. T.en
dc.contributor.authorKostova, I. P.en
dc.date.accessioned2024-04-05T16:35:17Z-
dc.date.available2024-04-05T16:35:17Z-
dc.date.issued2023-
dc.identifier.citationAlcolea Palafox, M, Belskaya, N, Todorov, L & Kostova, I 2023, 'Structural Study of a La(III) Complex of a 1,2,3-Triazole Ligand with Antioxidant Activity', Antioxidants, Том. 12, № 10, 1872. https://doi.org/10.3390/antiox12101872harvard_pure
dc.identifier.citationAlcolea Palafox, M., Belskaya, N., Todorov, L., & Kostova, I. (2023). Structural Study of a La(III) Complex of a 1,2,3-Triazole Ligand with Antioxidant Activity. Antioxidants, 12(10), [1872]. https://doi.org/10.3390/antiox12101872apa_pure
dc.identifier.issn2076-3921-
dc.identifier.otherFinal2
dc.identifier.otherAll Open Access, Gold, Green3
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85175324083&doi=10.3390%2fantiox12101872&partnerID=40&md5=90283e058bf85bca1df15a56beffe6af1
dc.identifier.otherhttps://www.mdpi.com/2076-3921/12/10/1872/pdf?version=1697530768pdf
dc.identifier.urihttp://elar.urfu.ru/handle/10995/130905-
dc.description.abstractThe 1,2,3-triazole derivative 2-(4-chlorophenyl)-5-(pyrrolidin-1-yl)-2H-1,2,3-triazole-4-carboxylic acid with potential anticancer activity was used as a ligand in complex formation with the lanthanum(III) ion. The molecular structure and vibrational spectra of the complex were optimized at three DFT levels, and the scaled IR and Raman spectra were compared to the experimental ones. Several scaling procedures were used. Through a detailed analysis, the structure predicted for the newly synthetized La(III) complex was confirmed by the good accordance of the calculated/experimental IR and Raman spectra. The best DFT method appeared to be M06-2X with the Lanl2mb basis set, followed closely by Lanl2dz. The effect of the lanthanide atom on the molecular structure and atomic charge distribution of the triazole ring was evaluated. The potential free radical scavenging activity of both the ligand and the complex was investigated in several radical-generating model systems. The potential mechanisms of antioxidant action (hydrogen atom transfer (HAT) and single-electron transfer (SET)) were elucidated. © 2023 by the authors.en
dc.description.sponsorshipBG-RRP-2.004-0004-C01en
dc.description.sponsorshipThis study was financed by the European Union-NextGenerationEU, through the National Recovery and Resilience Plan of the Republic of Bulgaria, project no. BG-RRP-2.004-0004-C01.en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.rightscc-byother
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/unpaywall
dc.sourceAntioxidants2
dc.sourceAntioxidantsen
dc.subject1,2,3-TRIAZOLESen
dc.subjectANTIOXIDANTen
dc.subjectLANTHANUMen
dc.subjectSCALINGen
dc.subjectVIBRATIONAL ANALYSISen
dc.titleStructural Study of a La(III) Complex of a 1,2,3-Triazole Ligand with Antioxidant Activityen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.type|info:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.3390/antiox12101872-
dc.identifier.scopus85175324083-
local.contributor.employeeAlcolea Palafox, M., Department of Physical Chemistry, Faculty of Chemical Sciences, Complutense University, Madrid, 28040, Spainen
local.contributor.employeeBelskaya, N.P., Department of Technology for Organic Synthesis, Ural Federal University, 19 Mira Str, Yekaterinburg, 620012, Russian Federationen
local.contributor.employeeTodorov, L.T., Department of Chemistry, Faculty of Pharmacy, Medical University—Sofia, 2 Dunav Str, Sofia, 1000, Bulgariaen
local.contributor.employeeKostova, I.P., Department of Chemistry, Faculty of Pharmacy, Medical University—Sofia, 2 Dunav Str, Sofia, 1000, Bulgariaen
local.issue10-
local.volume12-
dc.identifier.wos001119483800001-
local.contributor.departmentDepartment of Physical Chemistry, Faculty of Chemical Sciences, Complutense University, Madrid, 28040, Spainen
local.contributor.departmentDepartment of Technology for Organic Synthesis, Ural Federal University, 19 Mira Str, Yekaterinburg, 620012, Russian Federationen
local.contributor.departmentDepartment of Chemistry, Faculty of Pharmacy, Medical University—Sofia, 2 Dunav Str, Sofia, 1000, Bulgariaen
local.identifier.pure47594069-
local.description.order1872-
local.identifier.eid2-s2.0-85175324083-
local.identifier.wosWOS:001119483800001-
Располагается в коллекциях:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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