204
Views
0
CrossRef citations to date
0
Altmetric
Research Article

Chromogenic detection of fluoride, dihydrogen phosphate, and arsenite anions based on 2,4-dinitrophenyl hydrazine receptors: spectral and electrochemical study

, , &
Pages 534-549 | Received 20 Apr 2022, Accepted 05 Jun 2022, Published online: 07 Jul 2022
 

ABSTRACT

The colorimetric recognition of biologically relevant fluoride (F), acetate (AcO), and dihydrogen phosphate (H2PO4) ions, and poisonous arsenite (AsO2) ions, was devised and new receptors for these anions synthesised via the Schiff base condensation procedure. UV–visible titration, fluorescence titration, 1H-NMR titration, and cyclic voltammetry were used to explore the interactions of receptors R1–R3 with anions and possible detection mechanisms. The synthesised probes could sense inorganic fluoride, acetate, dihydrogen phosphate, and arsenite in the organo–aqueous medium (H2O/ Dimethylsulphoxide, 1: 9, v/v) and displayed a change in colour detectable to the naked eye. Out of the three synthesised receptors, receptor R1 showed better sensing ability of fluoride, acetate, dihydrogen phosphate, and arsenite ions in the organo–aqueous medium with a lower detection limit of 0.1 ppm, 0.171 ppm, 0.194 ppm, and 0.144 ppm, respectively. All three receptors formed complexes with the anions through H-bonding interaction followed by deprotonation of the NH proton.

Graphical Abstract

Acknowledgments

The authors convey their gratefulness to the Director and HOD (Department of Chemistry), NITK, Surathkal, for providing access to the research infrastructure. NK and AS are grateful to NITK for the research fellowship. The authors thank MIT, Manipal for help in 1H-NMR and 13C-NMR analysis, Mangalore university for mass analysis, and STIC, Cochin for the CHN analysis.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Supplementary material

Supplemental data for this article can be accessed online at https://doi.org/10.1080/10610278.2022.2087524.

Additional information

Funding

The author(s) reported that there is no funding associated with the work featured in this article.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.