Abstract Metal-organic frameworks (MOFs) have become a versatile platform for gas capture/separation and luminescent sensing of toxic pollutants, and the combination of both of these properties depends on the robust… Click to show full abstract
Abstract Metal-organic frameworks (MOFs) have become a versatile platform for gas capture/separation and luminescent sensing of toxic pollutants, and the combination of both of these properties depends on the robust framework and pre-designed pore functionality which is critical to achieve the targeted applications. In this work, a novel Cd(II)-MOF {(NH2Me2)[Cd3 (μ3-OH) (tpt) (TZB)3](H2O)2 (1,4-dioxane)5}n (1, H2TZB = 4-(1H-tetrazol-5-yl)benzoic acid, tpt = 2,4,6-tri (pyridin-4-yl)-1,3,5-triazine) comprising of a {Cd3(OH)}5+ cluster-based unit (SBU) has been solvothermally formed from nitrogen-rich and highly fluorescent organic ligands. The porous structure 1 is composed of cages and segments which are affixed by high density of free nitrogen atoms. The activated Cd(II)-MOF (1a) exhibits a relative high C2H2 sorption capacity than that of CO2 which endows it with a C2H2/CO2 sorption selectivity of 7.26 at room temperature. Furthermore, complex 1 could behave as a luminescent sensor for highly discriminative detection of explosive 2,4,6-trinitrophenol (TNP) via remarkable fluorescence quenching (Ksv = 6.16✕104 M−1).
               
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