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By adding 4,4′-bipyridine (BPY) to cross-link the paddle-wheel clusters M2(–COO)4L2, isoreticular metal–organic frameworks (MOFs) have been constructed from a flexible tritopic linker, 4,4′,4′′-s-triazine-1,3,5-triyltri-p-aminobenzoic acid (H3TATAB), termed as ST-14 [Cu6(TATAB)4(BPY)3] and… Click to show full abstract
By adding 4,4′-bipyridine (BPY) to cross-link the paddle-wheel clusters M2(–COO)4L2, isoreticular metal–organic frameworks (MOFs) have been constructed from a flexible tritopic linker, 4,4′,4′′-s-triazine-1,3,5-triyltri-p-aminobenzoic acid (H3TATAB), termed as ST-14 [Cu6(TATAB)4(BPY)3] and ST-15 [Zn6(TATAB)4(BPY)3]. With a secondary-amine group, these MOFs have shown exculsive cationic dye capture properties with charge selectivity, metal-dependent adsorption kinetics, and solvent-dependent dye release. This work sheds light on further designing smart porous materials for drug delivery, molecular inclusion, sensing and so on.
Journal Title: Materials Chemistry Frontiers
Year Published: 2018
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