4.6 Article

Two novel macrocyclic organotin(IV) carboxylates based on amide carboxylic acids

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RSC ADVANCES
卷 4, 期 6, 页码 3096-3101

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c3ra46198j

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Two novel macrocyclic organotin(IV) carboxylates [(n-Bu2Sn)L-1](2)center dot C7H8 (1) (L-1 = 2-(4-carboxyphenylcarbamoyl) benzoic acid) and [(n-Bu2Sn)L-2](3)center dot H2O (2) (L-2 = 5-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)isophthalic acid) were generated by the reactions of dibutyltin oxide with amide dicarboxylic acids and characterized by elemental analysis, IR, H-1 and C-13 NMR spectroscopy. X-ray crystallography diffraction analyses reveal that 1 is a di-nuclear dicarboxylate ring and 2 is a trinuclear tricarboxylate macrocycle. With the help of intermolecular interactions, 1 and 2 construct supramolecular 3D architectures filled with cavities. Free toluene and water molecules are located in the cavities of 1 and 2 respectively as guests. Thermal analyses suggest that complex 2 is thermally more stable than 1. The antitumour activity of 1 and 2 has also been studied.

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