Journal
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
Volume 446, Issue -, Pages -Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jphotochem.2023.115168
Keywords
Chemosensor; Chelation; FRET; Reversibility; Rhodamine; Fluorimetric probe
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In this work, we have designed and synthesized a novel fluorescent chemosensor, NR-HG, based on a naphthalimide-based rhodamine platform for the detection of Hg2+ ions. The probe shows high selectivity and sensitivity towards Hg2+ ions, operating through PET, CHEF, and FRET mechanisms. DFT analysis confirms the experimental observations. Cell imaging experiments demonstrate the compatibility of the probe with living cells and its effectiveness in real-life imaging.
In this work, we are presenting the design and synthesis of an innovative fluorescent chemosensor: NR-HG, established on a naphthalimide-based rhodamine platform for Hg2+ ion sensing. The probe operates via PET, CHEF, and FRET mechanisms. The fluorescent chemosensor shows an immense selectivity and sensitivity towards Hg2+ ion via the enhancement of ring-opening rhodamine spiro-cyclic structure, with a detection limit (LOD) of 491 nM. The DFT analysis strongly validates the experimental observations. The probe senses the Hg2+ ion reversibly upon the addition of potassium iodide (KI). From the analysis of Job's plot, it can be conclusively confirmed that the NR-HG-Hg2+ complex demonstrates a 1:1 stoichiometric ratio. We also conducted an MTT assay and cell imaging experiment to assess both the compatibility of the probe with living cells and its effectiveness in real-life imaging.
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