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An ultrasensitive colorimetric and fluorescent “turn-on” chemosensor based on Schiff base for the detection of Cu2+ in the aqueous medium

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Abstract

We designed and synthesized a fluorescent “turn-on” and colorimetric chemosensor ((E)-1-((p-tolylimino)methyl)naphthalen-2-ol) SB. The structure of the synthesized chemosensor was investigated by 1H NMR, FT-IR, and fluorescence spectroscopy, and its sensing properties were studied toward Mn2+, Cu2+, Pb2+, Cd2+, Na+, Ni2+, Al3+, K+, Ag+, Zn2+, Co2+, Cr3+, Hg2+, Ca2+, and Mg2+. SB showed an excellent colorimetric (yellow to yellowish brown) in MeOH and fluorescence “turn-on” sensing response to Cu2+ in MeOH/Water (10/90, v/v) media. The sensing mechanism of SB toward Cu2+ was investigated by FT-IR, 1H NMR titration, DFT studies, and Job’s plot analysis. The detection limit was calculated to be very low 0.0025 µg mL−1 (0.0025 ppm). Furthermore, the test strip containing SB also showed excellent selectivity and sensitivity toward Cu2+ in a solution medium and when supported on a solid medium.

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All data generated or analyzed during this study are included in this published article. All authors have read, understood, and have complied as applicable with the statement on “Ethical responsibilities of Authors” as found in the Instructions for Authors.

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Acknowledgements

The researchers would like to acknowledge Deanship of Scientific Research, Taif University for funding this work.

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Contributions

Sikandar Khan: conceptualization, data curation and writing—original draft; Mian Muhammad: supervision and project administration; Waheed Kamran: formal analysis and conceptualization; Hamed M. Al-Saidi: investigation, resources, and data curation; Salman S. Alharthi: editing and visualization; Jari S. Algethami: validation and investigation.

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Correspondence to Mian Muhammad.

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Khan, S., Muhammad, M., Kamran, A.W. et al. An ultrasensitive colorimetric and fluorescent “turn-on” chemosensor based on Schiff base for the detection of Cu2+ in the aqueous medium. Environ Monit Assess 195, 633 (2023). https://doi.org/10.1007/s10661-023-11260-3

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  • DOI: https://doi.org/10.1007/s10661-023-11260-3

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