Abstract
A new near-infrared fluorescent “turn-on” chemodosimeter (probe 1) based on dicyanomethylene-4H-chromene fluorophore for sulfide was developed. Probe 1 showed good fluorescence selectivity to sulfide over other anions and thiol-containing compounds. The discrimination of sulfide from disulfide could be achieved by comparison of the spectral difference of probe 1 after interaction with them. The absorption of probe 1 at 437 nm decreased, accompanied by red-shifting to 470 nm as a shoulder, and a strong peak at 610 nm appeared in the presence of sulfide. The absorption of 1 was slightly red-shifted to 452 nm with increased absorbance in the presence of disulfide. Probe 1 showed more than 1000-fold fluorescence enhancement at 712 nm with a Stokes shift of 102 nm in the presence of sulfide. The probe exhibited a good sensitivity in detection of sulfide with a wide pH span (4.0–11.0). The absorption change and fluorescence enhancement could be attributed to thiolysis of the dinitrophenyl ether group in probe 1 by the sulfide. The proposed mechanism was proved by 1H NMR spectra and EI-MS explorations. The probe was successfully applied for the detection of sulfide anions in real water samples.
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The authors thank the National Natural Science Foundation of China (No. 21102037) and Henan Agricultural University (Nos. KF1609, KF1720 and 201710466) for the financial support.
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Xie, P., Zhu, Y., Huang, X. et al. A new near-infrared fluorescent chemodosimeter for discrimination of sulfide from disulfide. Res Chem Intermed 44, 2823–2837 (2018). https://doi.org/10.1007/s11164-018-3263-x
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DOI: https://doi.org/10.1007/s11164-018-3263-x