Abstract

Ten new coordination polymers, namely, [Zn(L)(H2O)] (1), [Zn(L)(biim-4)0.5]·2H2O (2), [Zn(L)(biim-6)0.5]·2H2O (3), [Zn(L)(BTE)0.5(H2O)]·H2O (4), [Zn(L)(phen)]·H2O (5), [Cu(L)(phen)]·H2O (6), [Cd(L)(phen)] (7), [Cd5(L)5(biim-4)2.5]·5H2O (8), [Co(L)(biim-4)0.5(H2O)]·H2O (9), and [Ni(L)(biim-4)0.5(H2O)]·2H2O (10), where H2L = 3-carboxy-1-(4′-carboxybenzyl)-2-oxidopyridinium, biim-4 = 1,1′-(1,4-butanediyl)bis(imidazole), biim-6 = 1,1′-(1,6-hexanedidyl)bis(imidazole), BTE = 1,1′-(2,2′-oxybis(ethane-2,1-diyl))bis(1H-1,2,4-triazole), and phen = 1,10-phenanthroline, have been synthesized under hydrothermal conditions. These complexes were structurally characterized by single-crystal X-ray diffraction analyses and further characterized by infrared spectra (IR), elemental analyses, powder X-ray diffraction (PXRD) and thermogravimetric analyses (TGA). Compound 1 displays a 2D undulated layer structure. Compounds 2 and 3 exhibit the similar 1D chain structures. In 2, the adjacent chains are extended into a 3D supramolecular architecture via hydrogen-bonding interactions and π–π interactions. In 3, the adjacent chains are extended into a 3D supramolecular architecture via hydrogen-bonding interactions. Compound 4 shows a 1D chain structure. The adjacent chains are further extended into a 3D supramolecular architecture through π–π interactions. Compounds 5 and 6 are isomorphous, and show the same 1D chain structures. The chains are linked by hydrogen-bonding interactions into a 3D supramolecular architecture. Compound 7 shows a 1D chain structure. The chains are arranged on parallel levels in two directions, resulting in a plywood-like structure. Compound 8 displays an unusual 2D 2-fold parallel interpenetrating network with both polyrotaxane and polycatenane characters. Compound 9 shows a 2D 3-connected 63 network. The structure of compound 10 is an intriguing 2D self-penetrating network. In addition, the photoluminescent properties of 1–5, 7 and 8 have also been investigated in detail.

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