Synthesis and characterization of coordination polymers of a carboxylato cyclophane with metal [Zn(II) and Cd(II)]-2,2′-bipyridines

N,N′,N′′,N′′′-Tetrakis(3-carboxy-propionyl)-1,6,20,25-tetraaza-[6.1.6.1] paracyclophane, H4cp has been complexed with metal (Zn(II) and Cd(II)) 2,2′-bipyridyls. The resulting complexes of the composition [{Zn(2,2′-bpy)}2(cp)]n·4H2O 1 and [{Cd(2,2′-bpy)}2(cp)]n·5H2O 2 (2,2′-bpy = 2,2′-bipyridine) have been characterized using spectroscopic (IR, solid state UV–Vis), elemental analysis and single-crystal X-ray diffraction measurements. In these complexes the cyclophane coordinates in different modes, and in complex 2, Cd(II) is hepta-coordinated. However, under harsh reaction conditions (using excess nitric acid and a longer reaction time) debranching of the cyclophane is observed in the reaction of Zn(2,2′-bpy)(NO3)2 with H4cp, and a complex of the composition [Zn(2,2′-bpy)(Suc)]n3 (suc = succinate) is isolated. Using non-covalent interactions, complexes 1 and 2 provide 3D supramolecular structures, whereas an infinite 1D chain structure is observed for complex 3. The thermal and photoluminescence properties of the complexes have also been studied.

The reaction of N,N′,N′′,N′′′-tetrakis(3-carboxy-propionyl)-1,6,20,25-tetraaza-[6.1.6.1] paracyclophane with M(2,2′-bpy)(NO3)2·H2O (M = Zn(II)/Cd(II)) separately provides a variety of coordination polymers with 3D supramolecular structures.Figure optionsDownload as PowerPoint slide