Dergi makalesi Açık Erişim
Kose, Mahmut; Orhan, Ersin; Suzuki, Kazushi; Tutar, Ahmet; Unlu, Cihansel Sancak; Yokoyama, Yasushi
<?xml version='1.0' encoding='UTF-8'?> <record xmlns="http://www.loc.gov/MARC21/slim"> <leader>00000nam##2200000uu#4500</leader> <datafield tag="245" ind1=" " ind2=" "> <subfield code="a">Preparation and photochromic properties of 2,3-bisarylbenz[f]indenones</subfield> </datafield> <datafield tag="909" ind1="C" ind2="4"> <subfield code="p">JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY</subfield> <subfield code="v">257</subfield> <subfield code="c">50-53</subfield> </datafield> <controlfield tag="001">14199</controlfield> <datafield tag="980" ind1=" " ind2=" "> <subfield code="a">user-tubitak-destekli-proje-yayinlari</subfield> </datafield> <datafield tag="520" ind1=" " ind2=" "> <subfield code="a">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.</subfield> </datafield> <datafield tag="650" ind1="1" ind2="7"> <subfield code="2">opendefinition.org</subfield> <subfield code="a">cc-by</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Duzce Univ, Fac Arts & Sci, Dept Chem, TR-81620 Duzce, Turkey</subfield> <subfield code="a">Orhan, Ersin</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Yokohama Natl Univ, Grad Sch Engn, Dept Adv Mat Chem, Yokohama, Kanagawa 2408501, Japan</subfield> <subfield code="a">Suzuki, Kazushi</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Sakarya Univ, Fac Arts & Sci, Dept Chem, TR-54187 Sakarya, Turkey</subfield> <subfield code="a">Tutar, Ahmet</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Sakarya Univ, Fac Arts & Sci, Dept Chem, TR-54187 Sakarya, Turkey</subfield> <subfield code="a">Unlu, Cihansel Sancak</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Yokohama Natl Univ, Grad Sch Engn, Dept Adv Mat Chem, Yokohama, Kanagawa 2408501, Japan</subfield> <subfield code="a">Yokoyama, Yasushi</subfield> </datafield> <datafield tag="980" ind1=" " ind2=" "> <subfield code="b">article</subfield> <subfield code="a">publication</subfield> </datafield> <datafield tag="542" ind1=" " ind2=" "> <subfield code="l">open</subfield> </datafield> <datafield tag="100" ind1=" " ind2=" "> <subfield code="u">Bulent Ecevit Univ, Fac Arts & Sci, Dept Chem, TR-67100 Zonguldak, Turkey</subfield> <subfield code="a">Kose, Mahmut</subfield> </datafield> <datafield tag="260" ind1=" " ind2=" "> <subfield code="c">2013-01-01</subfield> </datafield> <controlfield tag="005">20210315081652.0</controlfield> <datafield tag="909" ind1="C" ind2="O"> <subfield code="o">oai:zenodo.org:14199</subfield> <subfield code="p">user-tubitak-destekli-proje-yayinlari</subfield> </datafield> <datafield tag="856" ind1="4" ind2=" "> <subfield code="z">md5:a2bbae2c9b97152ec452dfc0e339ab38</subfield> <subfield code="s">221</subfield> <subfield code="u">https://aperta.ulakbim.gov.trrecord/14199/files/bib-58cec9ce-49fe-4ec5-870e-14423ebdf3fd.txt</subfield> </datafield> <datafield tag="540" ind1=" " ind2=" "> <subfield code="u">http://www.opendefinition.org/licenses/cc-by</subfield> <subfield code="a">Creative Commons Attribution</subfield> </datafield> <datafield tag="024" ind1=" " ind2=" "> <subfield code="a">10.1016/j.jphotochem.2013.01.012</subfield> <subfield code="2">doi</subfield> </datafield> </record>
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