Abstract
The synthesis and characterization of a novel NIR region fluoride sensor, that makes use of the aza-boron-dipyrromethene (aza-BODIPY) fluorophore, is described. An arylmagnesium bromide was formed by reacting 4-bromophenol with a tert-butyldimethylsilyl protecting group and magnesium, which was then used to prepare the aza-BODIPY through a reaction with phthalonitrile. The unusually strong affinity between the fluoride anion and silicon is used to create a sensor dye, which exhibits a highly specific, rapid colorimetric and 'turn-off' fluorescence response for F- in solution and in living HeLa cells. With F-, there is enhanced intramolecular charge transfer within the S1 state and this results in efficient nonradiative decay and hence in a marked decrease in fluorescence emission intensity. This journal is
Original language | English |
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Pages (from-to) | 53864-53869 |
Number of pages | 6 |
Journal | RSC Advances |
Volume | 4 |
Issue number | 96 |
DOIs | |
Publication status | Published - 2014 |
ASJC Scopus subject areas
- Chemistry(all)
- Chemical Engineering(all)