<p>In this study, probe <b>T</b> is synthesized via a condensation reaction from 7-diethylamino-3-formylcoumarin and 2-(quinolin-8-yloxy) acetohydrazide. It demonstrates a strong recognition ability for Cu<sup>2+</sup> and S<sup>2−</sup> in the CH<sub>3</sub>CN/HEPES (9:1, <i>V</i>/<i>V</i>, pH = 7.34) buffer system. Upon the addition of Cu<sup>2+</sup>, the probe solution undergoes a visible color change from yellow-green to brown-yellow, with a noticeable red shift of 30&#xa0;nm in the maximum absorption wavelength. Under UV light, the solution fluorescence is significantly quenched, with a quenching rate of 98.6% and a detection limit of 0.289 µmol/L. The complex <b>T</b>-Cu<sup>2+</sup> formed by probe <b>T</b> and Cu<sup>2+</sup> enables continuous recognition of S<sup>2−</sup>, demonstrating a fluorescence recovery phenomenon with a recovery rate of 88.9% and a detection limit of 0.01 µmol/L. Probe <b>T</b> demonstrates excellent recognition ability for Cu<sup>2+</sup> and S<sup>2−</sup> at pH 4 ~ 9 and can be recycled for 4 times. Additionally, probe <b>T</b> was effectively employed in fabricating test strips for the rapid and convenient detection of Cu<sup>2+</sup> and S<sup>2−</sup>, and for determining Cu<sup>2+</sup> and S<sup>2−</sup> in living cells, owing to its excellent permeability and low cytotoxicity.</p>

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Synthesis of a Quinoline-Coumarin Fluorescent Probe and its Applications

  • Mingya Wang,
  • Junli Shi,
  • Duanlin Cao,
  • Linxiu Zhao

摘要

In this study, probe T is synthesized via a condensation reaction from 7-diethylamino-3-formylcoumarin and 2-(quinolin-8-yloxy) acetohydrazide. It demonstrates a strong recognition ability for Cu2+ and S2− in the CH3CN/HEPES (9:1, V/V, pH = 7.34) buffer system. Upon the addition of Cu2+, the probe solution undergoes a visible color change from yellow-green to brown-yellow, with a noticeable red shift of 30 nm in the maximum absorption wavelength. Under UV light, the solution fluorescence is significantly quenched, with a quenching rate of 98.6% and a detection limit of 0.289 µmol/L. The complex T-Cu2+ formed by probe T and Cu2+ enables continuous recognition of S2−, demonstrating a fluorescence recovery phenomenon with a recovery rate of 88.9% and a detection limit of 0.01 µmol/L. Probe T demonstrates excellent recognition ability for Cu2+ and S2− at pH 4 ~ 9 and can be recycled for 4 times. Additionally, probe T was effectively employed in fabricating test strips for the rapid and convenient detection of Cu2+ and S2−, and for determining Cu2+ and S2− in living cells, owing to its excellent permeability and low cytotoxicity.