Selective fluoride sensing by a novel series of lanthanide-based one-dimensional coordination polymers through intramolecular proton transfer.

A novel series of one-dimensional coordination polymers (CPs) is achieved via a facile one-pot synthesis strategy employing the nitrate salts of trivalent lanthanides, a pentadentate chelating ligand, and triphenylphosphine oxide at a controlled stoichiometry under ambient conditions. All the CPs are characterized comprehensively using spectroscopic, X-ray crystallographic and magnetometric studies. The CPs are found to be thermally stable up to a significantly high temperature and resistant to water for an indefinite time. They are photoactive and exhibit selective fluoride ion (F - ) sensing with excellent efficiency both colorimetrically and fluorimetrically in the solid-state as well as in solution. The presence of F - concomitantly sensitizes the photoluminescence enhancement and visual decolourization of the CPs in solution owing to the ground-state intra-molecular proton transfer. The photophysical response of the CPs to F - in solution was found to be instantaneous (<30 s). The sensitivity of detection is observed to be significantly high over a wide range of F - concentrations, covering the beneficial and detrimental domains of F - concentrations in drinking water. The limit of detection (LoD) under ambient conditions was found to be in the micromolar (μM) range-the best being 0.22 μM found using UV-vis spectrometry and 7.5 μM using fluorimetry. In comparison, the USEPA standard cut-off for the upper limit of F - concentration in drinking water is 211 μM, and the LoD of measuring F - concentration using the USEPA standard method using a fluoride-selective electrode is 26.3 μM. The CPs display markedly high selectivity toward F - with negligible-to-no interference from the commonly abundant ions (Cl - , Br - , I - , CH 3 CO 2 - , CO 3 2- , SO 4 2- , HPO 4 2- , NH 4 + , Na + , K + , Mg 2+ , and Ca 2+ ) in terms of UV-vis spectral change. Moreover, they also exhibit solid-state IR-spectrometric sensitivity towards F - under ambient conditions.