Abstract

A series of transition metal coordination polymers [Co(H 3L) 2(4,4′- bpy)(H 2O) 2] n∙n(4,4′-bpy) ( 1), [Ni(H 2L)(4,4′-bpy)(H 2O) 2] n ( 2), [Co 2(L)(phen) 2(H 2O) 4] n∙(H 2O) 2n ( 3), and [Ni 2(L)(phen) 2(H 2O) 4] n∙(H 2O) 2n ( 4) have been assembled from a semirigid multicarboxylate ligand 3,3′-(1,4-phenylenebis(oxy))diphthalic acid (H 4L) with the help of 4,4′-bipyridine (4,4′-bpy) ligand or 1,10-phenanthroline (phen) ligand. X-ray single crystal diffraction analysis reveals that complex 1 crystallizes in the space group of P − 1 and displays a one-dimensional (1D) chain structure constructed from 4,4′-bpy ligand and H 3L ligand, which was further interlinked to form a three-dimensional network via hydrogen bonds. In complex 2, Ni(II) atoms are coordinated by L ligand in monodentate fashion to form alternate left- and right-helices, which are further bridged together by the coordination interactions between Ni(II) atoms and 4,4′-bpy, leading to a 2-fold (4, 4)-connected interpenetrating network. Isostructural complexes 3 and 4 belong to the space group P − 1 and display a 1D chain structure constructed from phen and L ligands, which was further interlinked to form a 2D plane via π–π interactions. In addition, their thermal and luminescent properties were also investigated.

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