Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 Feb 19:8:14.
doi: 10.3389/fchem.2020.00014. eCollection 2020.

A Fluorescent and Colorimetric Chemosensor for Hg2+ Based on Rhodamine 6G With a Two-Step Reaction Mechanism

Affiliations

A Fluorescent and Colorimetric Chemosensor for Hg2+ Based on Rhodamine 6G With a Two-Step Reaction Mechanism

Cui-Bing Bai et al. Front Chem. .

Abstract

A fluorescent and colorimetric chemosensor L based on rhodamine 6G was designed, synthesized, and characterized. Based on a two-step reaction, the chemosensor L effectively recognized Hg2+. The interaction between the chemosensor and Hg2+ was confirmed by ultraviolet-visible spectrophotometry, fluorescence spectroscopy, electrospray ionization-mass spectrometry, Fourier-transform infrared spectroscopy, and frontier molecular orbital calculations. The chemosensor L was also incorporated into test strips and silica gel plates, which demonstrated good selectivity and high sensitivity for Hg2+.

Keywords: Hg2+; chemosensor; rhodamine 6G; silica gel plates; test strips.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Strategies for the chemosensing of Hg2+. Type A: The coordination between ligand and Hg2+. Type B: The desulfurization between ligand and Hg2+. Type C: The two-step reaction mechanism.
Figure 2
Figure 2
Synthesis of chemosensor L. (A) Compound A. (B) Compound B. (C) Compound C.
Figure 3
Figure 3
(A) Absorption spectra of L (1.0 × 10−5 M) in the presence of various metal ions in HEPES buffer. (B) Photographs of L (1.0 × 10−5 M) in the presence of various metal ions.
Figure 4
Figure 4
(A) Fluorescence spectra of L (1.0 × 10−5 M) in the presence of various metal ions in HEPES buffer (λex = 526 nm). (B) Photographs of chemosensor L (1.0 × 10−5 M) in the presence of various metal ions under the hand-held ultraviolet lamp.
Figure 5
Figure 5
Proposed mechanism for Hg2+ detection by chemosensor L.
Figure 6
Figure 6
(A) Fluorescence spectra of L (1.0 × 10−5 M) in the presence of different concentrations of Hg2+ in HEPES buffer (λex = 526 nm). (B) Plot of fluorescence intensity at 550 nm vs. Hg2+ concentration in the range of 0.1–3.0 equiv.
Figure 7
Figure 7
Molecular orbital plots (VESTA software) of the HOMOs and LUMOs of L, LO, and LO–Hg2+.
Figure 8
Figure 8
Photographs of test strips and silica gel plates.

References

    1. Alibert A., Vaiano P., Caporale A., Consales M., Ruvo M., Cusano A. (2017). Fluorescent chemosensors for Hg2+ detection in aqueous environment. Sens. Actuators B Chem. 247, 727–735. 10.1016/j.snb.2017.03.026 - DOI
    1. Bai C. B., Fan H. Y., Qiao R., Wang S. N., Wei B., Meng Q., et al. (2019). Synthesis of methionine methyl ester-modified coumarin as the fluorescent-colorimetric chemosensor for selective detection Cu2+ with application in molecular logic gate. Spectrochim. Acta. A 216, 45–51. 10.1016/j.saa.2019.03.016 - DOI - PubMed
    1. Bai C. B., Qiao R., Liao J. X., Xiong W. Z., Zhang J., Chen S. S., et al. (2018). A highly selective and reversible fluorescence “off-on-off” chemosensor for Hg2+ based on rhodamine-6G dyes derivative and its application as a molecular logic gate. Spectrochim. Acta. A 202, 252–259. 10.1016/j.saa.2018.05.050 - DOI - PubMed
    1. Chen X., Pradhan T., Wang F., Kim J. S., Yoon J. (2011). Fluorescent chemosensors based on spiroring-opening of xanthenes and related derivatives. Chem. Rev. 112, 1910–1956. 10.1021/cr200201z - DOI - PubMed
    1. Chen Y., Zhu C., Yang Z., Li J., Jiao Y., He W., et al. (2012). A new “turn-on” chemodosimeter for Hg2+: ICT fluorophore formation via Hg2+-induced carbaldehyde recovery from 1, 3-dithiane. Chem. Commun. 48, 5094–5096. 10.1039/c2cc31217d - DOI - PubMed

LinkOut - more resources