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Three Anionic Indium-Organic Frameworks for Highly Efficient and Selective Dye Adsorption, Lanthanide Adsorption, and Luminescence Regulation.

Xiangjing GaoGuohao SunFayuan GeHe-Gen Zheng
Published in: Inorganic chemistry (2019)
Through solvothermal reaction of InCl3 and tetracarboxylate ligands with different substituent groups on diphenyl ethers, three new anionic indium-organic frameworks have been successfully prepared. They are {[(CH3)2NH2]In(G-1)(H2O)}·9DMF (1), {[(CH3)2NH2]In(G-2)}·15DMF (2), and {[(CH3)2NH2]2In2(G-3)2}·16DMF (3) {DMF = N, N'-dimethylformamide; H4(G-1) = 5',5″″-oxybis(2'-methoxy[1,1':3',1″-terphenyl]-4,4″-dicarboxylic acid); H4(G-2) = 5',5″″-oxybis(2'-amino[1,1':3',1″-terphenyl]-4,4″-dicarboxylic acid); H4(G-3) = 5',5″″-oxybis([1,1':3',1″-terphenyl]-4,4″-dicarboxylic acid)}. Compounds 1-3 can be simplified as unimodal 4-connected frameworks with different topological types: lon, cag, and dia, respectively. Compounds 1 and 3 display 2-fold interpenetrating nets, while compound 2 is non-interpenetrating. Compounds 1 and 3 can adsorb cationic methylene blue (MB) with good capacity and a high adsorption rate due to their anionic frameworks and channel-type voids. In particular, compound 1 exhibits great selectivity for cationic MB in the mixtures of MB and methyl orange. In addition, the adsorption behavior of rare earth ions (Eu3+ and Tb3+) on compounds 1 and 3 has also been studied. Due to the different structural features and channel sizes of compounds 1 and 3 caused by different substituents on the ligands, the adsorption properties of rare earth ions on the two compounds are different.
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