Preparation and photochromic properties of 2,3-bisarylbenz[f]indenones

dc.contributor.authorKöse, Mahmut
dc.contributor.authorOrhan, Ersin
dc.contributor.authorSuzuki, Kazushi
dc.contributor.authorTutar, Ahmet
dc.contributor.authorÜnlü, Cihansel Sancak
dc.contributor.authorYokoyama, Yasushi
dc.date.accessioned2020-04-30T23:21:31Z
dc.date.available2020-04-30T23:21:31Z
dc.date.issued2013
dc.departmentDÜ, Fen-Edebiyat Fakültesi, Kimya Bölümüen_US
dc.descriptionYOKOYAMA, Yasushi/0000-0002-8654-1320; Tutar, Ahmet/0000-0001-5524-8001; orhan, ersin/0000-0002-5461-1005en_US
dc.descriptionWOS: 000317442300008en_US
dc.description.abstractFrom 2,3-dibromobenz[f]indenone, four compound: 2,3-bis(5-methyl-2-phenyl-4-thiazolyl)benz [f]indenone 10, 2,3-bis(3,5-dimethyl-4-isoxazolyl)benz[f]indenone 20, 3-(3,5-dimethyl-4-isoxazolyl)-2-(5-methyl-2-phenyl-4-thiazolyl)benz[f]indenone 30 and 2,3-bis(5-methyl-2-phenyl-4-thiazolyl)benz[f]indenol 40 were prepared, and their photochromic properties were investigated. Among them, photochrome 10 (weak photochromic) and its bisthiazolylbenz[f]indenol derivative 40 displayed photochromism. During ring closure photoreaction, photochrome 40 showed high conversion ratio (98.4%) with low diastereomeric excess (38%). (C) 2013 Elsevier B.V. All rights reserved.en_US
dc.description.sponsorshipBulent Ecevit UniversityBulent Ecevit University [BAP2009-13-02-04]; TUBITAK (Scientific and Technical Research Council of Turkey)Turkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [209T117]; Department of Chemistry at Sakarya UniversitySakarya University; Scientific and Technical Research Council of Turkey (TUBITAK)Turkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [104T397]; TUBITAKTurkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK)en_US
dc.description.sponsorshipThe authors are grateful to Bulent Ecevit University (Grant No.: BAP2009-13-02-04), and TUBITAK (Scientific and Technical Research Council of Turkey) for the financial support of part of this work (Grant No.: 209T117).; The authors are indebted to the Department of Chemistry at Sakarya University and to The Scientific and Technical Research Council of Turkey (TUBITAK) for financial support (Grant No. 104T397). C.S.U. thanks TUBITAK for fellowships.en_US
dc.identifier.doi10.1016/j.jphotochem.2013.01.012en_US
dc.identifier.endpage53en_US
dc.identifier.issn1010-6030
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage50en_US
dc.identifier.urihttps://doi.org/10.1016/j.jphotochem.2013.01.012
dc.identifier.urihttps://hdl.handle.net/20.500.12684/4207
dc.identifier.volume257en_US
dc.identifier.wosWOS:000317442300008en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherElsevier Science Saen_US
dc.relation.ispartofJournal Of Photochemistry And Photobiology A-Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectDiaryletheneen_US
dc.subjectPhotochromismen_US
dc.subjectBisarylbenz[f]indenolsen_US
dc.subjectBisarylbenz[f]indenoneen_US
dc.titlePreparation and photochromic properties of 2,3-bisarylbenz[f]indenonesen_US
dc.typeArticleen_US

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