Under hydrothermal conditions, four new complexes [InCl2(Hphth)(4,4′-bipy)0.5(H2O)]·2H2O (H2phth = phthalic acid, 4,4′-bipy = 4,4′-bipyridine) (1), [InCl4(4,4′-bipyH)(H2O)] (2), [InCl(Hphth)(nia)(H2O)2] (Hnia = nicotinic acid) (3), [InCl(Hnia)2(Hox)2]·3H2O (H2ox = oxalic acid) (4) were… Click to show full abstract
Under hydrothermal conditions, four new complexes [InCl2(Hphth)(4,4′-bipy)0.5(H2O)]·2H2O (H2phth = phthalic acid, 4,4′-bipy = 4,4′-bipyridine) (1), [InCl4(4,4′-bipyH)(H2O)] (2), [InCl(Hphth)(nia)(H2O)2] (Hnia = nicotinic acid) (3), [InCl(Hnia)2(Hox)2]·3H2O (H2ox = oxalic acid) (4) were synthesized by the reaction of Indium chloride (InCl3) as the metal source with H2phth, Hnia, 4,4′-bipy and H2ox as the ligands. The single-crystal X-ray diffraction analysis revealed that the complexes 1, 3 and 4 have 3D supramolecular structures with hydrogen bonding interactions and, complex 2 has an extended one-dimensional chain structure, which further forms a 2D supramolecular sheet structure. We discussed and proved the fluorescence sensing functions of these complexes for the different thiamine (TPP, TCl) biomolecules based on a “turn-on” manner. In addition, it is fascinating that these complexes have different potential adsorption characteristics and the adsorption performance of complex 1 was observed to be better than the others. The photoluminescence and dye selective adsorption properties of these complexes have been studied for the first time.
               
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