Hg(II)‐Mediated Intramolecular Cyclization of Alkynyl Hydrazones: Towards a New Reaction‐Based Sensing Approach for Hg(II) Ions
Drawing upon an intramolecular cyclization/annulation reaction sequence mediated by Hg2+ ions, a BODIPY‐based fluorescent probe decorated with an alkynyl hydrazone motif responds rapidly and selectively to Hg2+ ions, with a detection limit of 29 nM and a fluorescence turn‐on ratio of 15‐fold. With t...
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Veröffentlicht in: | Chemistry, an Asian journal an Asian journal, 2022-07, Vol.17 (13), p.e202200273-n/a |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Drawing upon an intramolecular cyclization/annulation reaction sequence mediated by Hg2+ ions, a BODIPY‐based fluorescent probe decorated with an alkynyl hydrazone motif responds rapidly and selectively to Hg2+ ions, with a detection limit of 29 nM and a fluorescence turn‐on ratio of 15‐fold. With the addition of Hg2+ ions, the BODIPY‐based alkynyl hydrazone transforms into a pyrazole ring to mediate a turn‐on emission response clearly observable to the naked eye under visible light excitation.
We constructed a new family of a reaction‐based fluorescent probe, which shows remarkable fluorescence enhancement (15‐fold), a low detection limit (29 nM), and relatively quick response time ( |
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ISSN: | 1861-4728 1861-471X |
DOI: | 10.1002/asia.202200273 |