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Please use this identifier to cite or link to this item: http://elar.urfu.ru/handle/10995/103103
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dc.contributor.authorMoseev, T. D.en
dc.contributor.authorLavrinchenko, I. A.en
dc.contributor.authorVaraksin, M. V.en
dc.contributor.authorPobedinskaya, D. Y.en
dc.contributor.authorDemidov, O. P.en
dc.contributor.authorBorovlev, I. V.en
dc.contributor.authorCharushin, V. N.en
dc.contributor.authorChupakhin, O. N.en
dc.date.accessioned2021-08-31T15:07:28Z-
dc.date.available2021-08-31T15:07:28Z-
dc.date.issued2021-
dc.identifier.citationMeso-functionalization of calix[4]arene with 1,3,7-triazapyrene in the design of novel fluorophores with the dual target detection of Al3+and Fe3+cations / T. D. Moseev, I. A. Lavrinchenko, M. V. Varaksin, et al. — DOI 10.1039/d0ra10605d // RSC Advances. — 2021. — Vol. 11. — Iss. 11. — P. 6407-6414.en
dc.identifier.issn20462069-
dc.identifier.otherFinal2
dc.identifier.otherAll Open Access, Gold3
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85100485666&doi=10.1039%2fd0ra10605d&partnerID=40&md5=6bc66d4a19706eba191343a1cc62852b
dc.identifier.otherhttps://pubs.rsc.org/en/content/articlepdf/2021/ra/d0ra10605dm
dc.identifier.urihttp://elar.urfu.ru/handle/10995/103103-
dc.description.abstractAmeso-functionalization strategy has successfully been applied to the synthesis of novel 1,3,7-triazapyrene derivatives of calixarenes. The key synthetic step in these transformations providing the direct C-C bond formation is nucleophilic substitution of hydrogen (SNH) in 1,3,7-triazapyrene. General photophysical characteristics for these macrocyclic compounds, as well as features in emission properties upon addition of various metal cations have been elaborated. Studies using NMR spectroscopy have also shown a mutual effect of both calix[4]arene and 1,3,7-triazapyrene moieties on the coordination process. The complex stoichiometry and binding constants for Al3+and Fe3+guests have been explored with titration experiments. © The Royal Society of Chemistry 2021.en
dc.description.sponsorshipThe research was financially supported by the Council on Grants of the President of the Russian Federation for State Support of Young Russian Scientists - Candidates of Sciences (Project No. MK-1196.2020.3, Agreement No. 075-15-2020-506).en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherRoyal Society of Chemistryen
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.sourceRSC Adv.2
dc.sourceRSC Advancesen
dc.subjectAROMATIC HYDROCARBONSen
dc.subjectNUCLEAR MAGNETIC RESONANCE SPECTROSCOPYen
dc.subjectTITRATIONen
dc.subjectC-C BOND FORMATIONen
dc.subjectCOORDINATION PROCESSen
dc.subjectEMISSION PROPERTIESen
dc.subjectFUNCTIONALIZATIONSen
dc.subjectMACROCYCLIC COMPOUNDSen
dc.subjectMESO-FUNCTIONALIZATIONen
dc.subjectNUCLEOPHILIC SUBSTITUTIONSen
dc.subjectPHOTOPHYSICAL CHARACTERISTICSen
dc.subjectPOSITIVE IONSen
dc.titleMeso-functionalization of calix[4]arene with 1,3,7-triazapyrene in the design of novel fluorophores with the dual target detection of Al3+and Fe3+cationsen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.rsi46744333-
dc.identifier.doi10.1039/d0ra10605d-
dc.identifier.scopus85100485666-
local.contributor.employeeMoseev, T.D., Ural Federal University, 19 Mira Str., Ekaterinburg, 620002, Russian Federation
local.contributor.employeeLavrinchenko, I.A., Ural Federal University, 19 Mira Str., Ekaterinburg, 620002, Russian Federation
local.contributor.employeeVaraksin, M.V., Ural Federal University, 19 Mira Str., Ekaterinburg, 620002, Russian Federation, Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, 22 S. Kovalevskaya Str., Ekaterinburg, 620990, Russian Federation
local.contributor.employeePobedinskaya, D.Y., North Caucasus Federal University, 1 Pushkin Str., Stavropol, 355009, Russian Federation
local.contributor.employeeDemidov, O.P., North Caucasus Federal University, 1 Pushkin Str., Stavropol, 355009, Russian Federation
local.contributor.employeeBorovlev, I.V., North Caucasus Federal University, 1 Pushkin Str., Stavropol, 355009, Russian Federation
local.contributor.employeeCharushin, V.N., Ural Federal University, 19 Mira Str., Ekaterinburg, 620002, Russian Federation, Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, 22 S. Kovalevskaya Str., Ekaterinburg, 620990, Russian Federation
local.contributor.employeeChupakhin, O.N., Ural Federal University, 19 Mira Str., Ekaterinburg, 620002, Russian Federation, Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, 22 S. Kovalevskaya Str., Ekaterinburg, 620990, Russian Federation
local.description.firstpage6407-
local.description.lastpage6414-
local.issue11-
local.volume11-
dc.identifier.wos000614616900064-
local.contributor.departmentUral Federal University, 19 Mira Str., Ekaterinburg, 620002, Russian Federation
local.contributor.departmentInstitute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, 22 S. Kovalevskaya Str., Ekaterinburg, 620990, Russian Federation
local.contributor.departmentNorth Caucasus Federal University, 1 Pushkin Str., Stavropol, 355009, Russian Federation
local.identifier.pure20889200-
local.identifier.pure7241f0ca-b190-4ac1-8536-01921215be5duuid
local.identifier.eid2-s2.0-85100485666-
local.identifier.wosWOS:000614616900064-
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