Hippuric acid–appended aminothiazole derivatives as ion-responsive metallogelators for visual detection of Ce³⁺

Abstract

A new class of hippuric acid–appended aminothiazole derivatives (1a–4a) was synthesized and systematically evaluated as potential ion‑responsive gelators in the presence of lanthanides such as Ce³⁺, Pr³⁺, Sm³⁺, and Eu³⁺, as well as other metal ions. Most metal–ligand interactions resulted in precipitates, crystalline solids, or clear solutions; however, ligand 2a uniquely induced gelation upon exposure to Ce³⁺ ions. Substituent effects were found to be decisive: a methyl group at the 4‑position of the thiazole ring strongly promoted gel formation, whereas methyl substitution at the 5‑position, phenyl substitution, or the absence of a methyl group exerted a weaker influence. This selective ion responsive gelation establishes a simple supramolecular platform for Ce³⁺ recognition. Importantly, ligand 2a enables rapid, instrument free, on site visual screening of highly contaminated samples, offering a practical and environmentally relevant approach for qualitative or semi quantitative monitoring. While not intended as a highly sensitive analytical method, this strategy highlights the trade-off between simplicity and detection limits compared to more sophisticated instrumental techniques, positioning it as a robust first line tool for environmental sensing applications.

Supplementary files

Article information

Article type
Paper
Submitted
07 Apr 2026
Accepted
24 Apr 2026
First published
24 Apr 2026

New J. Chem., 2026, Accepted Manuscript

Hippuric acid–appended aminothiazole derivatives as ion-responsive metallogelators for visual detection of Ce³⁺

P. Yadav, M. M. Saiyed and V. K. Sharma, New J. Chem., 2026, Accepted Manuscript , DOI: 10.1039/D6NJ01297C

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