1 Ocak 2013 Dergi makalesi Açık Erişim

Kose, Mahmut; Orhan, Ersin; Suzuki, Kazushi; Tutar, Ahmet; Unlu, Cihansel Sancak; Yokoyama, Yasushi

Dublin Core

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<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Kose, Mahmut</dc:creator>
  <dc:creator>Orhan, Ersin</dc:creator>
  <dc:creator>Suzuki, Kazushi</dc:creator>
  <dc:creator>Tutar, Ahmet</dc:creator>
  <dc:creator>Unlu, Cihansel Sancak</dc:creator>
  <dc:creator>Yokoyama, Yasushi</dc:creator>
  <dc:date>2013-01-01</dc:date>
  <dc:description>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.</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/14199</dc:identifier>
  <dc:identifier>oai:zenodo.org:14199</dc:identifier>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights>
  <dc:source>JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY 257 50-53</dc:source>
  <dc:title>Preparation and photochromic properties of 2,3-bisarylbenz[f]indenones</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
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