Selective fluorometric detection of aromatic thiols by a chemosensor containing two electrophilic sites with
Yasuhiro Shiraishi1, Kohei Yamamoto, Shigehiro Sumiya
1Research Center for Solar Energy Chemistry, and Division of Chemical Engineering, Graduate School of Engineering Science, Osaka University, Toyonaka 560-8531, Japan. shiraish@cheng.es.osaka-u.ac.jp.
Abstract:
A resorufin–dinitrophenyl ether conjugate (1) shows emission enhancement for aromatic thiols in aqueous media with a neutral–basic pH, while being nonemissive for aliphatic thiols. This is achieved by two electrophilic sites with different local softness on compound 1; the respective sites selectively react with aromatic or aliphatic thiolate anions.
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