Stable InterpenetratedZirconium-Based Metal–OrganicFramework for the Fluorescence Detection of MnO₄^–

In this work, a novel stable zirconium-based metal–organic framework (Zr-MOF) with the formula [Zr₆O₄(OH)₄(PVDC)₆]₄·66DMF (<b>Zr-1</b>, H₂PVDC = (<i>E</i>,<i>E</i>)-2,5-dimethoxy-1,4-bis­[2-(4-carboxylatestyryl)]­benzene; DMF = <i>N</i>,<i>N</i>-dimethylformamide) was synthesized by introducing a linear phenylenevinylene-based carboxylate ligand to react with ZrCl₄ under solvothermal conditions. According to single-crystal X-ray diffraction measurement, complex <b>Zr-1</b> featured a 2-fold interpenetrated framework, in which the single coordination framework possessed a structure similar to that of the well-known Zr-MOF, UiO-66, constructed from [Zr₆O₄(OH)₄]¹²⁺ clusters and carboxylate ligands PVDC^2–. Due to the introduction of the phenylenevinylene-functionalized ligand, complex <b>Zr-1</b> exhibited a unique fluorescence sensing performance toward permanganate (MnO₄^–) with different concentrations. At low concentrations, the fluorescence emission intensity of <b>Zr-1</b> around 510 nm was enhanced significantly with an increase in the concentration of MnO₄^– in an aqueous suspension. However, while excess MnO₄^– was added into the suspension, the fluorescence emission intensity decreased significantly, and the single emission peak turned into five emission peaks upon the addition of MnO₄^–. Such a phenomenon has been scarcely reported in previous MOF-based fluorescence sensors. Moreover, complex <b>Zr-1</b> showed high anti-interference capability for the detection of MnO₄^– both at low and high concentrations. This work may pave a new way for the development of MOF-based fluorescence sensing platforms.