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Preparation of pyrido[1,2-c][1,2,4]triazole-based π-conjugated triazene as a Fe3+ ion fluorescent sensor
A highly efficient coupling reaction of pyrido[1,2-c][1,2,4]triazole carbene precursors with sulfonyl azides leading to structurally diverse π-conjugated triazenes has been realized under very mild conditions. [Display omitted] A highly efficient coupling reaction of N-heterocyclic carbene precursor...
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Published in: | Chinese chemical letters 2019-05, Vol.30 (5), p.1059-1062 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A highly efficient coupling reaction of pyrido[1,2-c][1,2,4]triazole carbene precursors with sulfonyl azides leading to structurally diverse π-conjugated triazenes has been realized under very mild conditions.
[Display omitted]
A highly efficient coupling reaction of N-heterocyclic carbene precursors with sulfonyl azides has been developed, affording a variety of pyrido[1,2-c][1,2,4]triazole-based π-conjugated triazenes. The present reaction proceeds under very mild conditions with good functional group tolerance. The resulting triazenes exhibit selective and sensitive fluorescent response toward Fe3+ ion. |
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ISSN: | 1001-8417 1878-5964 |
DOI: | 10.1016/j.cclet.2019.01.013 |