Issue 15, 2011

Phthalide-derived novel fluoroionophores incorporating picolylamino receptors: synthesis and response to metal cations

Abstract

Phthalide derivatives incorporating mono- and di-picolylamino functionalities at the 6-position have been prepared as novel fluoroionophores and their fluorescence responses to metal cations have been investigated. These phthalides not only exhibited efficient fluorescence in an aqueous medium but also displayed fluorescence on–off response upon addition of transition-metal cations, namely Cu2+. The 6-aminophthalide fluorophore served as the core of the fluorescent probes although it has rarely been applied to a chemosensor. To the best of our knowledge, these modified phthalides are the first 6-aminophthalide-derived fluorometric probes for metal cations, namely Cu2+.

Graphical abstract: Phthalide-derived novel fluoroionophores incorporating picolylamino receptors: synthesis and response to metal cations

Supplementary files

Article information

Article type
Paper
Submitted
25 Mar 2011
Accepted
13 May 2011
First published
14 Jun 2011

Analyst, 2011,136, 3164-3169

Phthalide-derived novel fluoroionophores incorporating picolylamino receptors: synthesis and response to metal cations

H. Okamoto, A. Matsui and K. Satake, Analyst, 2011, 136, 3164 DOI: 10.1039/C1AN15239D

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