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Herein we report two new TPE‐based 3D MOFs, that is, Sr‐ETTB and Co‐ETTB (TPE=Tetraphenylethylene, H8ETTB=4′,4′′′,4′′′′′,4′′′′′′′‐(ethene‐1,1,2,2‐tetrayl)tetrakis(([1,1′‐biphenyl]‐3,5‐dicarboxylic acid))). Through tailoring outer shell electron configurations of SrII and CoII cations, the fluorescence intensity of the MOFs is tuned from high emission to complete non‐emission. Sr‐ETTB with strong blue fluorescence shows reversible fluorescence variations in response to pressure and temperature, which is directly related to the reversible deformation of the crystal structure. In addition, non‐emissive Co‐ETTB counterpart exhibits a turn‐on fluorescent enhancement under the stimulation of analyte histidine. In the process, TPE‐cored linkers in the MOFs are released through competitive coordination substitution and subsequently reassembled to perform aggregation‐induced luminescence behavior originated from the organic linkers. [ABSTRACT FROM AUTHOR]

Two new isostructural 3D lanthanide-organic frameworks [H2N(Me)2] [Ln3(OH)(bpt)3(H2O)3] (DMF)2⋅(H2O)4 ( 1-Ln; Ln=Sm and Eu) with a 1D channel (25 Å) have been successfully assembled from the rare trinuclear [Ln3(OH)(COO)9] clusters and biphenyl-3,4′,5-tricarboxylic acid (H3bpt) and exhibit high stability towards water in the pH range 3-10. MOF 1-Eu is a promising luminescent probe for sensing Fe3+ in aqueous solution and is also selective towards rhodamine B (RhB) with a superior adsorption capacity of 735 mg g−1, which is the highest among the reported Ln-MOFs for RhB removal so far. Periodic DFT calculations further confirmed the selective adsorption of rhodamine B over other dyes. [ABSTRACT FROM AUTHOR]

Two microporous complexes, [Zn(TATAB)(OCH3)] ⋅2 H3O+ ( 1; TATAB=4,4′,4′′-[(1,3,5-triazine-2,4,6-triyl)tris(azanediyl)]tribenzoic acid), [Cu1.5(μ2-O)TATAB*] ( 2; TATAB*=4,4′-{[6-(dimethylamino)-1,3,5-triazine-2,4-diyl]bis(azanediyl)}dibenzoic acid) have been synthesized and characterized by elemental analysis, IR spectroscopy, UV absorption spectroscopy, and thermogravimetric analysis, and by powder XRD and single-crystal XRD analysis. Structural analyses revealed that complex 1 possesses a 3D porous framework with uncoordinated water molecules trapped in the pores; the dimensions of the channels are approximately 29.2×12.3 Å2. Complex 2 has a 3D microporous network structure. In addition, the surface photovoltage and photocatalytic activities were also studied. The photocatalytic properties of the two complexes were investigated by the decomposition of methylene blue under UV and visible-light irradiation. The results revealed that 2 possessea a higher photocatalytic activity than 1 under UV or visible-light irradiation. The potential semiconductor and dye degradation properties of complexes 1 and 2 may be widely applied in the fields of chemical semiconductors and environmental protection in the future. [ABSTRACT FROM AUTHOR]