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A ratiometric fluorescent probe for fluoride ion employing the excited-state intramolecular proton transfer
Authors:Xiao-Feng Yang  Haiping Qi  Liping Wang  Zhuan Su  Gang Wang
Affiliation:Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, Institute of Analytical Science, Department of Chemistry, Northwest University, North Taibai Road 229#, Xi’an 710069, Shaanxi, China
Abstract:
A ratiometric fluorescent probe 1 for fluoride ion was developed based on modulation of the excited-state intramolecular proton transfer (ESIPT) process of 2-(2′-hydroxyphenyl)benzimidazole (HPBI) through the hydroxyl group protection/deprotection reaction. The probe 1 was readily prepared by the reaction of HPBI with tert-butyldimethylsilyl chloride (TBS-Cl) and shows only fluorescence emission maximum at 360 nm. Upon treatment with fluoride in aqueous DMF solution, the TBS protective group of probe 1 was removed readily and ESIPT of the probe was switched on, which resulted in a decrease of the emission band at 360 nm and an increase of a new fluorescence peak around 454 nm. The fluorescent intensity ratio at 454 and 360 nm (I454/I360) increases linearly with fluoride ion concentration in the range 0.3-8.0 μmol L−1 and the detection limit is 0.19 μmol L−1. The proposed probe shows excellent selectivity toward fluoride ion over other common anions. The method has been successfully applied to the fluoride determination in toothpaste and tap water samples.
Keywords:Fluoride ion   Fluorescent probe   2-(2&prime  -Hydroxyphenyl)benzimidazole   Ratiometric   Excited-state intramolecular proton transfer
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