Preparation and photochromic properties of 2,3-bisarylbenz[f]indenones
dc.contributor.author | Köse, Mahmut | |
dc.contributor.author | Orhan, Ersin | |
dc.contributor.author | Suzuki, Kazushi | |
dc.contributor.author | Tutar, Ahmet | |
dc.contributor.author | Ünlü, Cihansel Sancak | |
dc.contributor.author | Yokoyama, Yasushi | |
dc.date.accessioned | 2020-04-30T23:21:31Z | |
dc.date.available | 2020-04-30T23:21:31Z | |
dc.date.issued | 2013 | |
dc.department | DÜ, Fen-Edebiyat Fakültesi, Kimya Bölümü | en_US |
dc.description | YOKOYAMA, Yasushi/0000-0002-8654-1320; Tutar, Ahmet/0000-0001-5524-8001; orhan, ersin/0000-0002-5461-1005 | en_US |
dc.description | WOS: 000317442300008 | en_US |
dc.description.abstract | From 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.sponsorship | Bulent 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.sponsorship | The 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.doi | 10.1016/j.jphotochem.2013.01.012 | en_US |
dc.identifier.endpage | 53 | en_US |
dc.identifier.issn | 1010-6030 | |
dc.identifier.scopusquality | N/A | en_US |
dc.identifier.startpage | 50 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.jphotochem.2013.01.012 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12684/4207 | |
dc.identifier.volume | 257 | en_US |
dc.identifier.wos | WOS:000317442300008 | en_US |
dc.identifier.wosquality | Q2 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier Science Sa | en_US |
dc.relation.ispartof | Journal Of Photochemistry And Photobiology A-Chemistry | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Diarylethene | en_US |
dc.subject | Photochromism | en_US |
dc.subject | Bisarylbenz[f]indenols | en_US |
dc.subject | Bisarylbenz[f]indenone | en_US |
dc.title | Preparation and photochromic properties of 2,3-bisarylbenz[f]indenones | en_US |
dc.type | Article | en_US |
Dosyalar
Orijinal paket
1 - 1 / 1
Küçük Resim Yok
- İsim:
- 4207.pdf
- Boyut:
- 368.03 KB
- Biçim:
- Adobe Portable Document Format
- Açıklama:
- Tam Metin / Full Text