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dc.contributor.authorDemidov, O. P.-
dc.contributor.authorДемидов, О. П.-
dc.date.accessioned2023-01-26T09:15:12Z-
dc.date.available2023-01-26T09:15:12Z-
dc.date.issued2022-
dc.identifier.citationRostovtseva, I.A., Solov’eva, E.V., Voloshin, N.A., Chernyshev, A.V., Morozov, P.G., Devidov, O.P., Borodkin, G.S., Metelitsa, A.V. Photo- and Ionochromism of 1,3-Dihydrospiro[indole-2,2′-chromene] with Fluorescein Moiety // Russian Journal of General Chemistry. - 2022. - 92 (10), pp. 1906-1911. - DOI: 10.1134/S107036322210005Xru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/22248-
dc.description.abstractThe reaction of fluorescein-substituted 2-hydroxybenzaldehyde with 3H-indolium perchlorate has led to the formation of 1,3-dihydrospiro[indole-2,2′-chromene] bearing a fluorescein fragment at position 8 of chromene. In a solution, the obtained compound has existed in the cyclic form and has exhibited hotochromic properties. Adding transition metal perchlorates to the spiropyran solution has led to intense coloration due to the complex formation. Zinc and cadmium complexes of the spiropyran have exhibited red fluorescence and negative photochromism.ru
dc.language.isoenru
dc.relation.ispartofseriesRussian Journal of General Chemistry-
dc.subjectComplex formationru
dc.subjectFluorescenceru
dc.subjectFluoresceinru
dc.subjectSpiropyranru
dc.subjectMerocyanineru
dc.subjectPhotochromismru
dc.titlePhoto- and Ionochromism of 1,3-Dihydrospiro[indole-2,2′-chromene] with Fluorescein Moietyru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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