Multi responsive chemosensor for the determination of metal ions (Co2+, Cu2+, and Zn2+ ions)
Single probe (DBA) showed sensing behaviour towards multi ions having their low LOD values and its practical applicability was executed in real environmental samples. [Display omitted] •A multi-responsive chemosensor DBA was synthesized and characterized.•Single probe exhibited sensing behaviour tow...
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Veröffentlicht in: | Inorganic chemistry communications 2022-02, Vol.136, p.109181, Article 109181 |
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Sprache: | eng |
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Zusammenfassung: | Single probe (DBA) showed sensing behaviour towards multi ions having their low LOD values and its practical applicability was executed in real environmental samples.
[Display omitted]
•A multi-responsive chemosensor DBA was synthesized and characterized.•Single probe exhibited sensing behaviour towards Co2+, Cu2+, and Zn2+ ions with low LOD values.•The detection mechanism is supported by absorbance, fluorescence, job’s plot, HRMS, DFT.•Practical applicability was executed in different water samples.
A multi-responsive Schiff-based chemosensor 3-[1-(benzylimino)ethyl]-2-hydroxy-6-methyl-4H-pyran-4-one (DBA) was synthesized and characterized. Single probe (DBA) exhibited sensing behaviour towards Co2+, Cu2+, and Zn2+ ions. The binding approach of DBA towards Co2+, Cu2+, and Zn2+ ions was calculated on basis of jobs plot (1:1) and which was further confirmed on basis of the mass spectral technique. The detection limit of DBA towards Co2+, Cu2+ and Zn2+ ions was found to be 6.82 × 10-7 M, 9.74 × 10-8 M, and 1.14 × 10-7 M respectively. DFT computational studies also validated the results obtained from absorption and emission studies. Time-resolved fluorescence data suggested that the copper complex was more stable as compared to the cobalt and zinc complex. The stability of complex formed by DBA with Co2+, Cu2+, and Zn2+ ions were chequered by time-reliant studies. The synthesized Schiff base DBA can detect Co2+, Cu2+, and Zn2+ ions over a wide pH range, and its practical applicability was effectively executed in environmental water samples. |
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ISSN: | 1387-7003 1879-0259 |
DOI: | 10.1016/j.inoche.2021.109181 |