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Substituent Effects at the 5-Position of 3-[Bis(pyridine-2-ylmethyl)amino]-BODIPY Cation Sensor Used for Ratiometric Quantification of Cu2+
Title: | Substituent Effects at the 5-Position of 3-[Bis(pyridine-2-ylmethyl)amino]-BODIPY Cation Sensor Used for Ratiometric Quantification of Cu2+ |
Authors: | Hafuka, Akira Browse this author | Kando, Ryosuke Browse this author | Ohya, Kohei Browse this author | Yamada, Koji Browse this author →KAKEN DB | Okabe, Satoshi Browse this author →KAKEN DB | Satoh, Hisashi Browse this author →KAKEN DB |
Issue Date: | 15-Mar-2015 |
Publisher: | 日本化学会 |
Journal Title: | Bulletin of the Chemical Society of Japan |
Volume: | 88 |
Issue: | 3 |
Start Page: | 447 |
End Page: | 454 |
Publisher DOI: | 10.1246/bcsj.20140273 |
Abstract: | In this paper, we investigated the effects of substitution at the 5-position of an asymmetric BODIPY cation sensor to tune its spectroscopic, photophysical, and cation-sensing properties. We introduced substituent groups with differing electron density at the 5-position of 3-[bis(pyridine-2-ylmethyl)amino]-BODIPY, which contains a cation recognition moiety at the 3-position of the BODIPY core, to develop four sensors which all exhibited distinctive ratiometric spectral changes in the presence of Cu2+. Aromatic substitution increased the Stokes shift. Substitution with the electron-withdrawing sulfonylphenyl group resulted in the highest fluorescence quantum yield, largest absorption coefficient, and largest spectral shift in the presence of Cu2+. The sulfonylphenyl-substituted sensor also exhibited excellent selectivity for Cu2+. |
Type: | article (author version) |
URI: | http://hdl.handle.net/2115/58602 |
Appears in Collections: | 工学院・工学研究院 (Graduate School of Engineering / Faculty of Engineering) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)
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Submitter: 佐藤 久
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