Abstract

Two new lithium complexes and three coordination polymers with cesium, barium, and cadmium having deprotonated diclofenac acid (HDFA) ligand are reported. All these non-ionic complexes or the coordination polymers were characterized by single crystal X-ray diffraction, IR and thermal studies. The lithium-diclofenac complexes, [Li(DFA)(H2O)3] and [Li(DFA)(H2O)2(DMF)] were respectively obtained from reaction carried out in aqueous ethanol or dimethylformamide as solvent. Each formed hydrogen bonded 2D-sheets, which were further assembled into 3D-layers by involving edge-on Cl-π interactions. The respective average particle sizes determined by dynamic light scattering of the respective lithium complexes were 648.3 nm and 588.8 nm. The average particle size of the tri-aquated complex dissolved in water was decreased upon addition of dimethylformamide. The cesium coordination polymer [Cs(DFA)(μ-H2O)2]n had two-dimensional sheets formed through dative bonds. The hydrophobic parts of the sheets were projecting outward and two alternative sheets were inter-linked by edge-on chlorine-π interactions (3.391 Å) to provide 3-D supramolecular layered structure. One dimensional barium coordination polymer [Ba(DFA)2(H2O)4]n and a cadmium coordination polymer [{Cd(DMF)4}2+{Cd(DFA)4}2−]n having linear-chain structure were reported. The linear chain of the cadmium coordination polymer was comprised of the coordinatively linked assembly of complex cation [Cd(DMF)4]2+ with anion [Cd(DFA)4]2− located at alternative positions by side-on carboxylate bridges.

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