<p>A multi-metal colorimetric and fluorescent probe derived from 5-diethylamino salicylaldehyde and fluoresceinamine was synthesized, characterized and examined for metal ion sensing. In this probe, salicylaldehyde-derived Schiff base subunit provides an "O–N–N" coordination site for metal ion sensing, whereas fluoresceine is functioned as fluorogenic unit. The reported fluorescent probe showed fluorescence "<i>turn-on</i>" in response to metal ions in aqueous media with significant color changes from colorless to light green, yellow green and bright yellow upon binding with Cu<sup>2+</sup>, Ni<sup>2+</sup> and Zn<sup>2+</sup> ions, respectively. The synthesized probe simultaneously recognized these metal ions and distinguished by absorption and emission responses with detection limit of 0.25&#xa0;nM for Cu<sup>2+</sup>, 7.76&#xa0;nM for Ni<sup>2+</sup> and 38.22&#xa0;nM for Zn<sup>2+</sup> in HEPES buffer-methanol (2:1, v/v) solvent mixture.</p>

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An efficient fluorescein-based fluorescent chemosensor for quick detection of Cu2+, Zn2+ and Ni2+ ions

  • Aruna,
  • Arunava Agarwala,
  • Ved Prakash Verma,
  • Rahul Shrivastava

摘要

A multi-metal colorimetric and fluorescent probe derived from 5-diethylamino salicylaldehyde and fluoresceinamine was synthesized, characterized and examined for metal ion sensing. In this probe, salicylaldehyde-derived Schiff base subunit provides an "O–N–N" coordination site for metal ion sensing, whereas fluoresceine is functioned as fluorogenic unit. The reported fluorescent probe showed fluorescence "turn-on" in response to metal ions in aqueous media with significant color changes from colorless to light green, yellow green and bright yellow upon binding with Cu2+, Ni2+ and Zn2+ ions, respectively. The synthesized probe simultaneously recognized these metal ions and distinguished by absorption and emission responses with detection limit of 0.25 nM for Cu2+, 7.76 nM for Ni2+ and 38.22 nM for Zn2+ in HEPES buffer-methanol (2:1, v/v) solvent mixture.