Events9th International Electronic Conference on Sensors and Applications
Published
This submission belongs to the session A. Chemo- and Biosensors of the event 9th International Electronic Conference on Sensors and Applications
Published date
01 Nov, 2022
Academic Editor
author-avatarStefano Mariani
Citation
Nuna Ramos, Susana Costa, M. Manuela Raposo, A novel imidazole derivative: synthesis, characterization and chemosensory ability for ions , in Proceedings of 9th International Electronic Conference on Sensors and Applications, 1 November–15 November 2022, MDPI: Basel, Switzerland, doi: 10.3390/ecsa-9-13184
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A novel imidazole derivative: synthesis, characterization and chemosensory ability for ions

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1. Centre of Chemistry, Department of Chemistry, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal
2. Center of Chemistry, Department of Chemistry, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal
Abstract

Imidazoles have been explored over the past years as optical chemosensors due to their ability to coordinate with analytes. Heterocyclic molecules, are capable of providing specific binding sites, especially for ions. Consequently, a novel 2,4,5-triheteroarylimidazole was synthetized bearing indole and furyl moieties. The compound was characterized by the usual techniques, and the preliminary chemosensory ability was carried out in acetonitrile and acetonitrile/water (25:75) in the presence of ions with biological, medicinal, and environmental relevance. In aqueous medium, the new compound showed a slight enhancement of fluorescence in the presence of HSO4-. As for cations, it exhibited an enhancement of fluorescence with the addition of Fe2+, Sn2+, Fe3+ and Al3+ and a more pronounced quenching of fluorescence in the presence of Cu2+.

Keywords
imidazole
heterocycles
synthesis
fluorescent probe
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