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BODIPY-Based Ratiometric Fluoroionophores with Bidirectional Spectral Shifts for the Selective Recognition of Heavy Metal Ions
Title: | BODIPY-Based Ratiometric Fluoroionophores with Bidirectional Spectral Shifts for the Selective Recognition of Heavy Metal Ions |
Authors: | Hafuka, Akira Browse this author | Taniyama, Hiroki Browse this author | Son, Sang-Hyun Browse this author | Yamada, Koji Browse this author | Takahashi, Masahiro Browse this author | Okabe, Satoshi Browse this author | Satoh, Hisashi Browse this author →KAKEN DB |
Issue Date: | Jan-2013 |
Publisher: | Chemical Society of Japan |
Journal Title: | Bulletin of the Chemical Society of Japan |
Volume: | 86 |
Issue: | 1 |
Start Page: | 37 |
End Page: | 44 |
Publisher DOI: | 10.1246/bcsj.20120235 |
Abstract: | Two novel asymmetric BODIPY fluoroionophores with dipicolylamine (BDP-DPA, dipicolylamine: bis(pyridylmethyl)) and terpyridine (BDP-TPY) are described. These fluoroionophores display opposite wavelength responses on complexation with heavy metal ions. Furthermore, the fluorescence spectra vary depending on the ionic species. In particular, BDP-DPA shows a high affinity toward Cr3+ and upon complexation, the fluorescence spectrum blue-shifts from 591 to 566 nm. In contrast, BDP-TPY preferentially binds to Zn2+ and the fluorescence spectra red-shifts from 539 to 567 nm. BDP-TPY is the first example of asymmetric BODIPY with a pyridyl receptor at the 3 position showing redshifted fluorescence by complexation with metal ions. The concentration of each metal ion was successfully determined by ratiometric measurement. The wavelength-responses characteristics of these fluoroionophores could be very useful in the development of novel ratiometric fluoroionophores for metal ions. |
Type: | article |
URI: | http://hdl.handle.net/2115/52037 |
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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