Anthracene scaffold as highly selective chemosensor for Al3+ and its AIEE activity

Fluorescent chemosensor, 3-(Anthracen-2-yliminomethyl)-benzene-1,2-diol (ANB) has been synthesized by one-step condensation of 2-aminoanthracene and 2,3-dihydroxybenzaldehyde and characterized using 1 H-NMR, FT-IR and Mass spectroscopic techniques. The probe ANB was found to be an efficient ‘turn-on...

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Veröffentlicht in:Photochemical & photobiological sciences 2023-06, Vol.22 (6), p.1491-1503
Hauptverfasser: Mudi, Naren, Shyamal, Milan, Giri, Prabhat Kumar, Samanta, Shashanka Shekhar, Ramirez-Tagle, Rodrigo, Misra, Ajay
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Sprache:eng
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Zusammenfassung:Fluorescent chemosensor, 3-(Anthracen-2-yliminomethyl)-benzene-1,2-diol (ANB) has been synthesized by one-step condensation of 2-aminoanthracene and 2,3-dihydroxybenzaldehyde and characterized using 1 H-NMR, FT-IR and Mass spectroscopic techniques. The probe ANB was found to be an efficient ‘turn-on’ fluorescence chemosensor for the selective detection of Al 3+ ion over other metal ions in an aqueous solution. The chemosensor exhibits ~ 27-fold enhancement of emission intensity in presence of Al 3+ ion. Fluorescence quantum values for ANB and (Al 3+ -ANB)-complex are 0.004 and 0.097, respectively. In addition, the binding constant and the limit of detection were found to be 1.22 × 10 4  M −1 and 0.391 µM, respectively. The chemosensor ANB binds to Al 3+ ions in 2:1 stoichiometric ratio which was supported by Job’s plot, 1 H-NMR titration and florescence titration. Fluorescence reversibility of the sensor complex was well established by adding EDTA in the same condition and a molecular INHIBIT logic gate was fabricated using this reversible nature of the sensor complex. Additionally, the chemosensor ANB shows a novel aggregation-induced enhanced emission phenomenon, where the aggregate hydrosol of ANB shows enhance emission intensity. Graphical abstract
ISSN:1474-905X
1474-9092
DOI:10.1007/s43630-023-00392-7