Abstract

A series of structurally diverse coordination polymers, [Mn(ppmdc)(H2O)2]n (1), [Cu(ppmdc)(H2O)2]n (2), {[Co(ppmdc)][Co(ppmdc)(H2O)]}n (3), [Zn(ppmdc)(H2O)]n (4), and [Cd(ppmdc)]n (5) (H2ppmdc = 2-(pyridin-3-yl)-4,6-pyrimidine dicarboxylic acid) were obtained from metal salts and H2ppmdc under hydrothermal conditions. Single crystal X-ray structural analysis reveals that complexes 1–5 have different structures, ranging from one- to three-dimensions, which are mainly due to the different metal ions, and especially the coordination mode of the H2ppmdc ligand. Complexes 1 and 2 are 1D coordination polymers, in which the ppmdc2– ligand adopts a bis-(bidentate) mode to link metal ions. Complexes 3 and 4 feature a 2D metal-organic framework with Schläfli topologies of (4.62) (42.62.82) and (4.82), respectively, in which the metal ions are bridged by μ3-ppmdc2– ligands. Complex 5 possesses a 3D nanotubular metal-organic framework with a point symbol of (49.66) topology built up from the 6-connected ppmdc2– ligands and Cd(ii) ions. The thermal properties of complexes 1–5 have been determined. Moreover, investigation of photoluminescent properties reveals that the configuration of ppmdc2– resulting from metal-directed coordination has a profound effect on the fluorescence emissions of complexes 4 and 5.

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