Issue 23, 2011

Solid-state emissive triarylborane-based BODIPY dyes: Photophysical properties and fluorescent sensing for fluoride and cyanide ions

Abstract

We disclose two novel BODIPY dyes, which contain the bulky substituent, [(4-dimesitylboryl)phenyl]ethynyl at 2- and 2,6-positions. The steric bulkiness of the boryl group is effective to suppress the intermolecular interaction in the solid state and thus these two compounds display intense fluorescence not only in solution but also in the solid state. In addition, the BODIPY dyes display sensitive fluorescence responses to fluoride and cyanide anions through the complexation with the boron center of the boryl group and the subsequent decomposition of the BODIPY core, illustrating their potential uses for the fluorescence sensing of fluoride and cyanide ions.

Graphical abstract: Solid-state emissive triarylborane-based BODIPY dyes: Photophysical properties and fluorescent sensing for fluoride and cyanide ions

Supplementary files

Article information

Article type
Paper
Submitted
14 Jun 2011
Accepted
12 Sep 2011
First published
12 Sep 2011

Org. Biomol. Chem., 2011,9, 8141-8146

Solid-state emissive triarylborane-based BODIPY dyes: Photophysical properties and fluorescent sensing for fluoride and cyanide ions

G. Fu, H. Pan, Y. Zhao and C. Zhao, Org. Biomol. Chem., 2011, 9, 8141 DOI: 10.1039/C1OB05959A

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