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 |
|---|---|
| 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
Fingerprint
Dive into the research topics of 'A class of wavelength-tunable near-infrared aza-BODIPY dyes and their application for sensing mercury ion'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver