Rationally designed phenanthrene derivatized triazole as a dual chemosensor for fluoride and copper recognition

A 1,2,3-triazole chemosensor containing phenanthrene and phenol moieties (PhTP) was efficiently synthesized via copper (I)-catalyzed azide-alkyne cycloaddition, “click chemistry”. PhTP is a dual analyte sensor for fluoride and copper (II) ions in homogeneous medium. Deprotonation of the phenolic [sbnd]OH proton by the fluoride ion is responsible for a change in fluorescence color from blue (PhTP) to yellowish-orange (PhTP-fluoride adduct), while a charge transfer between the triazole nitrogen of the chemosensor and Cu²⁺ revealed a turn-off fluorescence output. The detection capability of PhTP was analyzed with a series of anions (F⁻, Cl⁻, Br⁻, I⁻, H₂PO₄ ⁻, ClO₄ ⁻, OAc⁻, BF₄ ⁻) and cations (Fe³⁺, Fe²⁺, Cu²⁺, Ag⁺, Cr³⁺, Al³⁺, Co²⁺, Ni²⁺, Cd²⁺, Zn²⁺). With anions, competitive fluorescence responses under UV lamp were observed for acetate and dihydrogen phosphate anions, but maximum response from fluoride ion was substantiated from steady state absorption and fluorescence experiments. With cations, PhTP displayed a selective and sensitive recognition towards Cu²⁺ ion through spectral modulation in absorption spectroscopy and a turn-off fluorescence response. Nuclear magnetic resonance (NMR) spectroscopic titration studies supported the results obtained through photophysical studies and provided evidence for the ion-binding sites on the probe.