Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
28799 | Journal of Photochemistry and Photobiology A: Chemistry | 2011 | 4 Pages |
Abstract
2,3-Bis(5-methyl-2-phenyl-4-thiazolyl)-1,4-naphthoquinone 1-O, its monoethylene acetal 2-O and methylated derivatives 3-O and 4-O were synthesized and their photochromic properties were investigated. While bisarylnaphthoquinone 1-O was nonphotochromic, its monoacetal 2-O and methylated derivatives 3-O and 4-O displayed good photochromism. Among them, the isomer 4-O recorded a remarkable diastereomeric excess (98.40%) with high conversion ratio (96.20%) upon UV irradiation.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Bioengineering
Authors
Mahmut Kose, Çiğdem Yıldırım Şekerci, Kazushi Suzuki, Yasushi Yokoyama,