Water-soluble bis-triazolyl benzochalcogendiazole cycloadducts as tunable metal ion sensors
A series of bis-triazolyl benzochalcogendiazoles was synthesized to investigate their metal-binding capabilities. These fluorophores were formed through the cycloaddition of an ethynylated benzochalcogendiazole and a water-soluble azide. Variation of the chalcogen heteroatom was seen to affect the p...
Gespeichert in:
| Hauptverfasser: | , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2013
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| In: |
The journal of organic chemistry
Year: 2013, Jahrgang: 78, Heft: 3, Pages: 1038-1044 |
| ISSN: | 1520-6904 |
| DOI: | 10.1021/jo3024889 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/jo3024889
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| Verfasserangaben: | Jonathan J. Bryant, Benjamin D. Lindner, and Uwe H.F. Bunz |
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| 520 | |a A series of bis-triazolyl benzochalcogendiazoles was synthesized to investigate their metal-binding capabilities. These fluorophores were formed through the cycloaddition of an ethynylated benzochalcogendiazole and a water-soluble azide. Variation of the chalcogen heteroatom was seen to affect the photophysical properties as well as the metal-binding activity. These cycloadducts exhibited a distinct response to Cu2+, Ni2+, and Ag+ in water. The binding affinity for the copper and nickel ions increased moving the chalcogen atom from O to Se. Statistical analysis of the spectral data enabled differentiation of Ag+, Cu2+, and Ni2+ ions. | ||
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