Abstract
Molecules containing polarized NH fragments that behave as anion-binding motifs are widely used as receptors for recognition and sensing purposes in aprotic solvents. We present here a new example of a receptor, 3-amino-5-(4,5,6,7-tetrahydro-1H-indol-2-yl)isoxazole-4-carboxamide (receptor 1), which contains pyrrole, amide and amino subunits. This receptor shows both changes in its UV-vis absorption and fluorescence emission spectra upon the addition of F-, resulting in highly selectivity for fluoride detection over other anions, such as Cl-, Br-, I -, HSO4-, H2PO4- and AcO- in CH3CN. 1H NMR titration, time-dependent density functional theory (TDDFT) calculations and other experiments confirm that the sensing process is brought about by deprotonation of the pyrrole-NH in receptor 1. © 2011 Yang et al; licensee Beilstein-Institut.
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CITATION STYLE
Yang, Z., Zhang, K., Gong, F., Li, S., Chen, J., Ma, J. S., … Trofimov, B. A. (2011). A new fluorescent chemosensor for fluoride anion based on a pyrrole-isoxazole derivative. Beilstein Journal of Organic Chemistry, 7, 46–52. https://doi.org/10.3762/bjoc.7.8
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