Abstract
A multifunctional colorimetric chemosensor 1, based on 4-(diethylamino)-2-hydroxybenzaldehyde and 2,3-diamino-5-bromopyridine, has been synthesized and characterized. Sensor 1 detected instantly both Cu2+ and S2− by the color change from pale yellow to deep yellow. The binding modes of 1 with Cu2+ and S2− were found to be the 1:1 stoichiometry through Job plot and ESI-mass spectrometry analysis, respectively. In addition, the detection limit of 1 for Cu2+ was found to be 68.6 nΜ which was much lower than WHO guideline (31.5 µΜ) in drinking water. Importantly, sensor 1 could be used to quantify Cu2+ in water samples. Moreover, 1 exhibited a high selectivity for S2− in the presence of other anions. The sensing mechanisms of Cu2+ and S2− by 1 were explained by theoretical calculations.
| Original language | English |
|---|---|
| Pages (from-to) | 709-717 |
| Number of pages | 9 |
| Journal | Inorganica Chimica Acta |
| Volume | 471 |
| DOIs | |
| State | Published - 24 Feb 2018 |
Keywords
- Colorimetric chemosensor
- Copper ion
- Naked-eye
- Sulfide
- Theoretical calculations
Fingerprint
Dive into the research topics of 'Selective detection of Cu2+ and S2− by a colorimetric chemosensor: Experimental and theoretical calculations'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver