Issue 10, 2015

A highly selective ratiometric bifunctional fluorescence probe for Hg2+ and F ions

Abstract

A triarylborane derivative BN-S, which contains a Hg2+-responsive dithioacetal group and a F-responsive boryl group, has been designed and synthesized via the functionalization of 2-dimesitylboryl-2′-(N,N-dimethylamino)biphenyl core skeleton with a dithioacetal substituent. This compound displays intense intramolecular charge transfer fluorescence, even for its nano-aggregates in water. The Hg2+-promoted deprotection of the dithioacetal group and complexation of F with the tri-coordinate boron center cause hypochromism of fluorescence to different extents. And thus BN-S behaves as a promising ratiometric bifunctional fluorescence probe to detect Hg2+ and F simultaneously. In addition, the detection of Hg2+ is performable in aqueous medium using its nano-aggregates.

Graphical abstract: A highly selective ratiometric bifunctional fluorescence probe for Hg2+ and F− ions

Supplementary files

Article information

Article type
Paper
Submitted
12 Dec 2014
Accepted
14 Jan 2015
First published
14 Jan 2015

Org. Biomol. Chem., 2015,13, 3032-3039

Author version available

A highly selective ratiometric bifunctional fluorescence probe for Hg2+ and F ions

Q. Xu, C. Wang, Z. Sun and C. Zhao, Org. Biomol. Chem., 2015, 13, 3032 DOI: 10.1039/C4OB02593H

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