1. Электронный научный архив УрФУ
  2. 00. Общеуниверситетские коллекции
  3. Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC
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dc.contributor.authorMohammed, M. S.en
dc.contributor.authorKovalev, I. S.en
dc.contributor.authorSlovesnova, N. V.en
dc.contributor.authorSadieva, L. K.en
dc.contributor.authorPlatonov, V. A.en
dc.contributor.authorKim, G. A.en
dc.contributor.authorAluru, R.en
dc.contributor.authorNovikov, A. S.en
dc.contributor.authorTaniya, O. S.en
dc.contributor.authorCharushin, V. N.en
dc.date.accessioned2024-04-05T16:28:05Z-
dc.date.available2024-04-05T16:28:05Z-
dc.date.issued2023-
dc.identifier.citationMohammed, MS, Kovalev, IS, Slovesnova, NV, Sadieva, LK, Platonov, VA, Kim, GA, Aluru, R, Novikov, AS, Taniya, OS & Charushin, VN 2023, '(1-(4-(5-Phenyl-1,3,4-oxadiazol-2-yl)phenyl)-1H-1,2,3-triazol-4-yl)-methylenyls α,ω-Bisfunctionalized 3- and 4-PEG: Synthesis and Photophysical Studies', Molecules, Том. 28, № 13, 5256. https://doi.org/10.3390/molecules28135256harvard_pure
dc.identifier.citationMohammed, M. S., Kovalev, I. S., Slovesnova, N. V., Sadieva, L. K., Platonov, V. A., Kim, G. A., Aluru, R., Novikov, A. S., Taniya, O. S., & Charushin, V. N. (2023). (1-(4-(5-Phenyl-1,3,4-oxadiazol-2-yl)phenyl)-1H-1,2,3-triazol-4-yl)-methylenyls α,ω-Bisfunctionalized 3- and 4-PEG: Synthesis and Photophysical Studies. Molecules, 28(13), [5256]. https://doi.org/10.3390/molecules28135256apa_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-s2.0-85164843919&doi=10.3390%2fmolecules28135256&partnerID=40&md5=16403e33c88c0989509b05254b5810031
dc.identifier.otherhttps://www.mdpi.com/1420-3049/28/13/5256/pdf?version=1688729188pdf
dc.identifier.urihttp://elar.urfu.ru/handle/10995/130640-
dc.description.abstractTwo new azaheterocycle-based bolas, such as (1-(4-(5-phenyl-1,3,4-oxadiazol-2-yl)phenyl)-1H-1,2,3-triazol-4-yl)-methylenyls α,ω-bisfunctionalized PEGs, were prepared via Cu-catalyzed click reaction between 2-(4-azidophenyl)-5-(aryl)-oxadiazole-1,3,4 and terminal ethynyls derived from PEG-3 and PEG-4. Due to the presence of two heteroaromatic cores and a PEG linker, these bola molecules are considered as promising fluorescent chemosensors for electron-deficient species. As a result of a well-pronounced “turn-off” fluorescence response towards common nitro-explosive components, such as 2,4-dinitrotoluene (DNT) and 2,4,6-trinitrotoluene (TNT), hard-to-detect pentaerythritol tetranitrate (PETN), as well as Hg2+ cation was observed. © 2023 by the authors.en
dc.description.sponsorshipRussian Academy of Sciences, РАН; Ministry of Education and Science of the Russian Federation, Minobrnauka: 075-15-2022-1118; RUDN Universityen
dc.description.sponsorshipThe quantum chemical calculations were supported by the RUDN University Strategic Academic Leadership Program; the absolute quantum yields were measured using the equipment of the Center for Joint Use “Spectroscopy and Analysis of Organic Compounds” at the Postovsky Institute of Organic Synthesis of the Russian Academy of Sciences (Ural Branch).en
dc.description.sponsorshipThis research was funded by the Ministry of Science and Higher Education of the Russian Federation (Reference # 075-15-2022-1118, dated 29 June 2022).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.sourceMolecules2
dc.sourceMoleculesen
dc.subjectBOLA MOLECULESen
dc.subjectFLUORESCENCEen
dc.subjectFLUORESCENCE QUENCHINGen
dc.subjectHG2+en
dc.subjectNITRO-EXPLOSIVE COMPONENTSen
dc.subjectOXADIAZOLEen
dc.subjectPEGSen
dc.subjectPENTAERYTHRITOL TETRANITRATEen
dc.subjectSENSORen
dc.subject“CLICK” REACTIONSen
dc.subjectEXPLOSIVEen
dc.subjectTRINITROTOLUENEen
dc.subjectEXPLOSIVE AGENTSen
dc.subjectTRINITROTOLUENEen
dc.title(1-(4-(5-Phenyl-1,3,4-oxadiazol-2-yl)phenyl)-1H-1,2,3-triazol-4-yl)-methylenyls α,ω-Bisfunctionalized 3- and 4-PEG: Synthesis and Photophysical Studiesen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.type|info:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.3390/molecules28135256-
dc.identifier.scopus85164843919-
local.contributor.employeeMohammed, M.S., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federationen
local.contributor.employeeKovalev, I.S., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federationen
local.contributor.employeeSlovesnova, N.V., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federation, Department of Pharmacy and Chemistry, Ural Medical University, 3 Repina St, Yekaterinburg, 620028, Russian Federationen
local.contributor.employeeSadieva, L.K., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federationen
local.contributor.employeePlatonov, V.A., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federationen
local.contributor.employeeKim, G.A., I. Ya. Postovsky Institute of Organic Synthesis of RAS (Ural Division), 22/20 S. Kovalevskoy/Akademicheskaya St, Yekaterinburg, 620137, Russian Federation, Institute of Natural Sciences and Mathematics, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federationen
local.contributor.employeeAluru, R., 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 Street, Moscow, 117198, Russian Federationen
local.contributor.employeeTaniya, O.S., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federationen
local.contributor.employeeCharushin, V.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, 620137, Russian Federationen
local.issue13-
local.volume28-
dc.identifier.wos001030864500001-
local.contributor.departmentChemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federationen
local.contributor.departmentDepartment of Pharmacy and Chemistry, Ural Medical University, 3 Repina St, Yekaterinburg, 620028, Russian Federationen
local.contributor.departmentI. Ya. Postovsky Institute of Organic Synthesis of RAS (Ural Division), 22/20 S. Kovalevskoy/Akademicheskaya St, Yekaterinburg, 620137, Russian Federationen
local.contributor.departmentInstitute of Natural Sciences and Mathematics, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, 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 Street, Moscow, 117198, Russian Federationen
local.identifier.pure41991074-
local.description.order5256-
local.identifier.eid2-s2.0-85164843919-
local.identifier.wosWOS:001030864500001-
local.identifier.pmid37446917-
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