Fluorescence properties of 2-aryl substituted indoles |
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Authors: | Nakazono Manabu Saita Kenichiro Oshikawa Yuji Tani Kazushi Nanbu Shinkoh Zaitsu Kiyoshi |
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Institution: | Graduate School of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan. nakazono@phar.kyushu-u.ac.jp |
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Abstract: | The fluorescence properties of 2-phenylindole, 2-naphthylindole and 2-anthracenylindole were investigated. 2-Anthracenylindole was newly synthesized by Suzuki-Miyaura's coupling. The fluorescence quantum yield of 2-phenylindole was the highest and the fluorescence emission maximum wavelength of 2-anthracenylindole was the longest. The ab initio quantum chemical calculation of the 2-anthracenylindole showed that the HOMO and LUMO of 2-anthracenylindole were localized in the anthracene moiety. |
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