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A simple TICT/ICT based molecular probe exhibiting ratiometric fluorescence Turn-On response in selective detection of Cu2+

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dc.contributor.authorRai, Ravisen
dc.contributor.authorBhandari, Rimpi
dc.contributor.authorKaleem, Mohammed
dc.contributor.authorRai, Nilesh
dc.contributor.authorGautam, Vibhav
dc.contributor.authorMisra, Arvind
dc.date.accessioned2025-01-28T09:42:53Z
dc.date.available2025-01-28T09:42:53Z
dc.date.issued2023
dc.description.abstractThe work reported herein describes photophysical behavior of a new fluorescent probe APDA. The probe exhibited sensitivity for Cu2+ ion in 80% aqueous acetonitrile medium. Probe shows dual emission due to TICT and ICT states and upon interaction with different metal ions Cu2+ induces hydrolysis of imine bond to rejuvenate aldehyde derivative with ratiometric �turn�On� fluorescence response, through ICT state while emission due to TICT state get diminished. Similarly, the synthesized model compound ADA under similar experimental condition supported hydrolysis of imine bond in the presence of copper. Jobs plot analysis, based on emission titration data suggested a 1:1 binding stoichiometry between probe APDA and Cu2+ ion. The limit of detection (LOD) was found to be 4.4 � 10-8 M (44 nM). The probe has been applied on test paper strip to detect Cu2+ ion with naked-eye sensitive response. Also, the cell imaging studies revealed the potential applicability of probe to detect Cu2+ ion in live cells. The mechanism of sensing was confirmed by 1H, 13C NMR, FTIR and mass spectrometry data analysis. � 2023 Elsevier B.V.
dc.identifier.doihttps://doi.org/10.1016/j.jphotochem.2023.114696
dc.identifier.issn10106030
dc.identifier.urihttps://dl.bhu.ac.in/ir/handle/123456789/22128
dc.language.isoen
dc.publisherElsevier B.V.
dc.subjectAnthracene
dc.subjectDiaminomaleonitrile
dc.subjectFluorescence
dc.subjectRatiometric
dc.subjectTICT Chemodosimeter
dc.titleA simple TICT/ICT based molecular probe exhibiting ratiometric fluorescence Turn-On response in selective detection of Cu2+
dc.typeArticle
dspace.entity.typePublication
journal.titleJournal of Photochemistry and Photobiology A: Chemistry
journalvolume.identifier.volume441

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2023