Abstract

By adjusting the molar ratio of the reactant metal salt and ligands, three new entangled coordination polymers, [Cd(tib)(tbta)(H2O)]n (1) and [Cd(Htib)(tbta)·Htbta·2CH3OH]n (2) and [Cd2(tib)2(tbta)2(H2O)·10H2O]n (3) (tib = 1,3,5-tris(1-imidazolyl)benzene and H2tbta = tetrabromoterephthalic acid), have been prepared and structurally characterized by X-ray diffraction analyses. Complex 1 is a 2-fold interpenetrated three-dimensional (3D) 8-connected uninodal net with rare hex topology. Complex 2 presents a 2D 63-hcb network, which is interdigitated with each other to form the 3D supramolecular framework stabilized hydrogen bonds and halogen bonds. Interestingly, an unprecedented hydrogen-bonded [(Htbta)2(CH3OH)4] cluster was unmasked in the void of 2. Complex 3 is a complicated 3D self-penetrated framework with a point symbol of {4·6·8}{4·65·84}{66}, which can be seen as a pair of 2-fold interpenetrated networks by breaking bidentate-bridging tib ligand. The comparative study revealed that 1–3 are particularly sensitive to the metal–ligand ratio in this system. The thermal stabilities and photoluminescence behaviors of 1 and 2 were also discussed.

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