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dc.contributor.authorVerbitskiy, E. V.en
dc.contributor.authorAchelle, S.en
dc.contributor.authorBureš, F.en
dc.contributor.authorle, Poul, P.en
dc.contributor.authorBarsella, A.en
dc.contributor.authorKvashnin, Y. A.en
dc.contributor.authorRusinov, G. L.en
dc.contributor.authorGuen, F. R. -L.en
dc.contributor.authorChupakhin, O. N.en
dc.contributor.authorCharushin, V. N.en
dc.date.accessioned2021-08-31T14:57:19Z-
dc.date.available2021-08-31T14:57:19Z-
dc.date.issued2021-
dc.identifier.citationSynthesis, photophysical and nonlinear optical properties of [1,2,5]oxadiazolo[3,4-b]pyrazine-based linear push-pull systems / E. V. Verbitskiy, S. Achelle, F. Bureš, et al. — DOI 10.1016/j.jphotochem.2020.112900 // Journal of Photochemistry and Photobiology A: Chemistry. — 2021. — Vol. 404. — 112900.en
dc.identifier.issn10106030-
dc.identifier.otherFinal2
dc.identifier.otherAll Open Access, Bronze, Green3
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85091239260&doi=10.1016%2fj.jphotochem.2020.112900&partnerID=40&md5=0dda1f92f1bcb6cee4705cd06e214524
dc.identifier.otherhttps://doi.org/10.1016/j.jphotochem.2020.112900m
dc.identifier.urihttp://elar.urfu.ru/handle/10995/101443-
dc.description.abstractA series of D-π-A chromophores based on [1,2,5]oxadiazolo[3,4-b]pyrazine electron-withdrawing group has been designed. The influence of the π-conjugated linker (1,4-phenylene and 2,5-thienylene) and the amino-electron-donating group (diphenylamino and carbazol-9-yl) was studied by cyclic voltammetry, UV-Vis and emission spectroscopy. The second order nonlinear optical properties were also studied using the electric field induced second harmonic generation (EFISH) method. The experimental results have been rationalized by theoretical DFT calculations. © 2020 Elsevier B.V.en
dc.description.sponsorshipVEV is grateful to the financial support for the synthetic part from the Russian Foundation for Basic Research (Research Project No. 18-29-23045 mk).en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherElsevier B.V.en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.sourceJ. Photochem. Photobiol. A Chem.2
dc.sourceJournal of Photochemistry and Photobiology A: Chemistryen
dc.subjectDONOR–ACCEPTOR SYSTEMSen
dc.subjectFLUORESCENCEen
dc.subjectINTRAMOLECULAR CHARGE TRANSFERen
dc.subjectNITROGEN HETEROCYCLESen
dc.subjectNONLINEAR OPTICen
dc.titleSynthesis, photophysical and nonlinear optical properties of [1,2,5]oxadiazolo[3,4-b]pyrazine-based linear push-pull systemsen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.rsi45318143-
dc.identifier.doi10.1016/j.jphotochem.2020.112900-
dc.identifier.scopus85091239260-
local.contributor.employeeVerbitskiy, E.V., I. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, S. Kovalevskaya Str., 22, Ekaterinburg, 620108, Russian Federation, Ural Federal University, Mira St. 19, Ekaterinburg, 620002, Russian Federation
local.contributor.employeeAchelle, S., Univ Rennes, CNRS, Institut des Sciences Chimiques de Rennes-UMR6226, Rennes, F35000, France
local.contributor.employeeBureš, F., Institute of Organic Chemistry and Technology, Faculty of Chemical Technology, University of Pardubice, Studenská 573, Pardubice, 53210, Czech Republic
local.contributor.employeele Poul, P., Univ Rennes, CNRS, Institut des Sciences Chimiques de Rennes-UMR6226, Rennes, F35000, France
local.contributor.employeeBarsella, A., Département d'Optique ultrarapide et Nanophotonique, IPCMS, UMR CNRS 7504, Université de Strasbourg, 23 rue du Loess, BP 43, Strasbourg Cedex 2, 67034, France
local.contributor.employeeKvashnin, Y.A., I. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, S. Kovalevskaya Str., 22, Ekaterinburg, 620108, Russian Federation
local.contributor.employeeRusinov, G.L., I. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, S. Kovalevskaya Str., 22, Ekaterinburg, 620108, Russian Federation, Ural Federal University, Mira St. 19, Ekaterinburg, 620002, Russian Federation
local.contributor.employeeGuen, F.R.-L., Univ Rennes, CNRS, Institut des Sciences Chimiques de Rennes-UMR6226, Rennes, F35000, France
local.contributor.employeeChupakhin, O.N., I. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, S. Kovalevskaya Str., 22, Ekaterinburg, 620108, Russian Federation, Ural Federal University, Mira St. 19, Ekaterinburg, 620002, Russian Federation
local.contributor.employeeCharushin, V.N., I. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, S. Kovalevskaya Str., 22, Ekaterinburg, 620108, Russian Federation, Ural Federal University, Mira St. 19, Ekaterinburg, 620002, Russian Federation
local.volume404-
dc.identifier.wos000591664200006-
local.contributor.departmentI. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, S. Kovalevskaya Str., 22, Ekaterinburg, 620108, Russian Federation
local.contributor.departmentUral Federal University, Mira St. 19, Ekaterinburg, 620002, Russian Federation
local.contributor.departmentUniv Rennes, CNRS, Institut des Sciences Chimiques de Rennes-UMR6226, Rennes, F35000, France
local.contributor.departmentInstitute of Organic Chemistry and Technology, Faculty of Chemical Technology, University of Pardubice, Studenská 573, Pardubice, 53210, Czech Republic
local.contributor.departmentDépartement d'Optique ultrarapide et Nanophotonique, IPCMS, UMR CNRS 7504, Université de Strasbourg, 23 rue du Loess, BP 43, Strasbourg Cedex 2, 67034, France
local.identifier.pure13900168-
local.identifier.purecf11585d-d6ac-459a-b0ac-a833275d0e05uuid
local.description.order112900-
local.identifier.eid2-s2.0-85091239260-
local.fund.rffi18-29-23045-
local.identifier.wosWOS:000591664200006-
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