4.6 Article

A chromone based Schiff base: An efficient colorimetric sensor for specific detection of Cu (II) ion in real water samples

Journal

JOURNAL OF MOLECULAR STRUCTURE
Volume 1227, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.molstruc.2020.129549

Keywords

Schiff base; Colorimetric probe; Cu2+ ions; HRMS; LOD; Binding constant

Funding

  1. UGC-JRF from UGC, New Delhi [169(June 2018)/2019(NET/CSIR), 264/(CSIR-UGC NET JUNE 2018)]

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A new chromone based Schiff base ligand L was synthesized and successfully used as a colorimetric probe for selectively detecting Cu (II) ions, showing instant visual color change and high sensitivity. The ligand L exhibited a binding stoichiometry of 1:1 with Cu2+ ions, and demonstrated strong selectivity and effectiveness in identifying and quantifying Cu2+ ions in real water samples.
A new chromone based Schiff base ligand L was synthesized by the condensation of 3-formyl chromone and pyrazine-2-carbohydrazide as a colorimetric probe to detect Cu (II) ions selectively. An instant visual colour change from colourless to yellow was obtained on addition of Cu2+ ions to the probe L solution, while other metal ions found ineffective. The ligand L was characterized by H-1 NMR, FTIR and HRMS spectral techniques. UV-Visible spectroscopic technique was used to study the sensing ability of probe L for copper ions above other metal ions. The Job's plot obtained from absorption studies and HRMS data confirmed that the Cu2+ ions bind with ligand L in 1:1 stoichiometric ratio. DFT computations were also supported the binding framework between L and Cu (II) ions. The LOD value and the association constant were obtained 3.9 x 10(-7) M and 2.3 x 10(5) M-1 respectively, via Benesi-Hildebrand equation. Selectivity of L towards Cu2+ ions was also studied and it was found that the probe L worked specifically for copper ions without any considerable influence of other intruding metal ions. In addition, in real water samples, the ligand L was fully implemented for identification and quantification of Cu2+ ions. (C) 2020 Elsevier B.V. All rights reserved.

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