Abstract
We present the design, synthesis, photophysical properties and application for sensing mercury ion, of a series of excellent near infrared fluorescent aza-boron-dipyrromethene (aza-BODIPY) dyes. The introduction of different aromatic substituents to the aza-BODIPY core induced red-shifted absorption and emission wavelengths due to the extension of the π-system. In addition, "turn-off" fluorescence responses and solution color changes selectively toward mercury ion have also been realized. The Hg 2+-induced fluorescence quenching may be assigned to the energy or electron transfer from emissive aza-BODIPY core to Hg2+.
Original language | English |
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Pages (from-to) | 145-153 |
Number of pages | 9 |
Journal | Dyes and Pigments |
Volume | 103 |
DOIs | |
State | Published - Apr 2014 |
Externally published | Yes |
Keywords
- Aza-boron-dipyrromethene
- Carbazoles
- Fluorenes
- Mercury ion
- Near infrared
- Sensing