Abstract
A hexaphenyl-1, 3-butadiene derivative containing methylpyridinium moiety, 4, 4'-((1E, 1'E)-(((1E, 3E)-1, 2, 3, 4-tetraphenylbuta-1, 3-diene-1, 4-diyl)bis(1, 4-phenylene))bis(ethene-1, 2-diyl))bis(N-methylpyridinium) iodide (HPB-PyM), was firstly synthesized through Heck reaction of HPB-Br with 4-vinylpyridine and subsequent methylation with iodomethane. As the precursors of HPB-PyM, HPB-Br and HPB-Py showed excellent aggregation-induced emission characteristic. In contrast, HPB-PyM exhibited orange emission (λem=605 nm) in the solid state with aggregation-caused quenching (ACQ) characteristic. Moreover, the fluorescence of HPB-PyM via AIE mechanism could be lightened and significantly enhanced by Hg2+ ions. As a “turn on” probe, HPB-PyM not only exhibited a rapid, sensitive, and selective response towards Hg2+ but also achieved linear and colorimetric detection for Hg2+ with a detection limit of 4.153 μmol/L.
| Original language | English |
|---|---|
| Pages (from-to) | 513-525 |
| Number of pages | 13 |
| Journal | Yingxiang Kexue yu Guanghuaxue/Imaging Science and Photochemistry |
| Volume | 34 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - 1 Nov 2016 |
Keywords
- Detection of Hg
- Hexaphenyl-1, 3-butadiene derivative
- High-selective
- “turn-on” fluorescent response
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