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Highly selective and sensitive detection of Hg2+ by a novel fluorescent probe with dual recognition sites.

Authors :
Li, Hongqi
Li, Jiayin
Pan, Zhixiu
Zheng, Tao
Song, Yanxi
Zhang, Jian
Xiao, Zhongwen
Source :
Spectrochimica Acta Part A: Molecular & Biomolecular Spectroscopy. Apr2023, Vol. 291, pN.PAG-N.PAG. 1p.
Publication Year :
2023

Abstract

[Display omitted] • A fluorescent probe with dual recognition sites for Hg2+ was developed. • Addition of Hg2+ induced fluorescence enhancement of the probe by 70 fold. • The probe turned from colorless to blackish brown upon addition of Hg2+ ion. • The probe showed low LOD of 0.12 μM for sensing of Hg2+ ion. • It was used for bioimaging and determination of Hg2+ concentrations in real water samples. A novel thionocarbonate-coumarin-thiourea triad-based probe with dual recognition sites for sensing mercury (Hg2+) ion was developed. The synthesized probe possessed both fluorogenic ("off-on") and chromogenic (from colorless to blackish brown) sensing performance towards Hg2+ ions. The fluorescence intensity was increased by 70 fold after the addition of Hg2+. As expected, the probe exhibited excellent selectivity and sensitivity for Hg2+ compared to other common competitive metal ions. The fluorescence intensity of the probe improved linearly with the increase of the concentration of Hg2+ (0–40 μM). Also, the minimum limit of detection (LOD) of the synthesized probe was 0.12 μM. Considering the importance of test feasibility in the harsh environment, the developed probe was applicable for detecting Hg2+ ions over a broad working pH range of 3–11. It is reliable and qualifies for the quantitative determination of Hg2+ concentrations in actual water samples. Finally, the probe achieved the bioimaging performance of Hg2+ in living cells and plants with good biocompatibility. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13861425
Volume :
291
Database :
Academic Search Index
Journal :
Spectrochimica Acta Part A: Molecular & Biomolecular Spectroscopy
Publication Type :
Academic Journal
Accession number :
161905639
Full Text :
https://doi.org/10.1016/j.saa.2023.122379