Issue 3, 2011

A fluorometric/colorimetric dual-channel Hg2+ sensor derived from a 4-amino-7-nitro-benzoxadiazole (ANBD) fluorophore

Abstract

A new visible light excitable Hg2+ sensor, NBD-TAEE, was prepared by bridging a 4-amino-7-nitro-benzoxadiazole (ANBD) fluorophore with thiaazacrown ethervia an ethylene spacer. Besides the specific Hg2+-induced absorption shift from 466 to 513 nm, this sensor exhibits the specific Hg2+-induced emission enhancement (∼29-fold) and fluorescent pH-independence from pH 6 to 13. Hg2+ addition even leads to the emission red shift from 532 to 570 nm, although NBD-TAEE is not a ratiometric fluorescent sensor due to its emission band being overlaid by the Hg2+-induced band. The instant and reversible “turn-on” Hg2+ response, fine cell permeability and cell imaging ability display its potential application in both environmental and Hg2+-polluted biological samples. Its analogue without the ethylene spacer, NBD-TAE, possesses the higher quantum yield and very poor Hg2+ binding ability. Their different emission behavior and sensing ability suggest that the spacer is quite essential for sensor construction.

Graphical abstract: A fluorometric/colorimetric dual-channel Hg2+ sensor derived from a 4-amino-7-nitro-benzoxadiazole (ANBD) fluorophore

Supplementary files

Article information

Article type
Paper
Submitted
10 Oct 2010
Accepted
10 Dec 2010
First published
07 Jan 2011

New J. Chem., 2011,35, 607-613

A fluorometric/colorimetric dual-channel Hg2+ sensor derived from a 4-amino-7-nitro-benzoxadiazole (ANBD) fluorophore

Z. Xie, K. Wang, C. Zhang, Z. Yang, Y. Chen, Z. Guo, G. Lu and W. He, New J. Chem., 2011, 35, 607 DOI: 10.1039/C0NJ00773K

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