METHOXY-SUBSTITUTED NAPHTHOTHIOPHENES – SINGLE MOLECULES' VS. CONDENSED PHASE PROPERTIES AND PROSPECTS FOR ORGANIC ELECTRONICS APPLICATIONS

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dc.contributor.authorBotezatu, Anatoly
dc.contributor.authorKhoroshutin, Andrey
dc.contributor.authorTokarev, Sergey
dc.contributor.authorLypenko, Dmitry A.
dc.contributor.authorTameev, Alexey
dc.contributor.authorFedorova, Olga
dc.date.accessioned2022-09-12T09:31:46Z
dc.date.available2022-09-12T09:31:46Z
dc.date.issued2022-08
dc.description.abstractIn this work, a series of tricyclic naphthothiophenes – photocyclization products (8- methoxynaphtho[1,2-b]thiophene (1a); 6,7-dimethoxynaphtho[1,2-b]thiophene (1b); 8- methoxynaphtho[2,1-b]thiophene (2a) have been studied. All compounds possessing similar structures demonstrated the close optical, electrochemical characteristics. Spectroelectrochemical investigation showed that 1b and 2a are able to form stable radical particles at 1.55 V. In case of 1a, the formed at 1.55 V radical is short-living.en_US
dc.identifier.citationBotezatu, A. Khoroshutin, A. Tokarev, S. Lypenko, Alexey Tameev, D.A. Fedorova, O. (2022). Methoxy-substituted naphthothiophenes – single molecules' vs. condensed phase properties and prospects for organic electronics applications. National Laboratory Astanaen_US
dc.identifier.urihttp://nur.nu.edu.kz/handle/123456789/6665
dc.language.isoenen_US
dc.publisherNational Laboratory Astanaen_US
dc.rightsAttribution-NonCommercial-ShareAlike 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/us/*
dc.subjectType of access: Embargoen_US
dc.subjecttricyclic naphthothiophenesen_US
dc.titleMETHOXY-SUBSTITUTED NAPHTHOTHIOPHENES – SINGLE MOLECULES' VS. CONDENSED PHASE PROPERTIES AND PROSPECTS FOR ORGANIC ELECTRONICS APPLICATIONSen_US
dc.typeAbstracten_US
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