Abstract
The fluoride anion (F-) sensing abilities of 1-hydroxyl-3,4,9,10-tetra (n-butoxyloxycarbonyl) perylene (probe 1) and 1-hydroxyl-mono-five-membered S-heterocyclic annulated tetra (n-butoxyloxycarbonyl) perylene (probe 2) were studied through visual detection experiments, UV-Vis, fluorescence, and 1H NMR titrations. The probes were sensitive and selective for distinguishing F- from other anions (Cl-, Br-, I-, SO4-, PF6-, H2PO4-, BF4-, ClO4-, OH-, CH3COO-, and HPO42-) through a change of UV-Vis and fluorescence spectra. The absorption and fluorescence emission properties of the probes arise from the intermolecular proton transfer (IPT) process between a hydrogen atom on the phenolic O position of probe and the F- anion. The sensing mechanism was supported by theoretical investigation. Moreover, probe-based test strips can conveniently detect F- without any additional equipment, and they can be used as fluorescent probes for monitoring F- in living cells.
Cite
CITATION STYLE
Zhang, F., Zhao, Y., Chi, Y., Ma, Y., Jiang, T., Wei, X., … Shi, J. (2018). Novel fluorescent probes for the fluoride anion based on hydroxy-substituted perylene tetra-(alkoxycarbonyl) derivatives. RSC Advances, 8(25), 14084–14091. https://doi.org/10.1039/c8ra00299a
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.