Abstract

The self-assembled di-nuclear Mn(III) & tetra-nuclear Cd(II) salamo-like oligo(N,O-donor) complexes, [Mn2(L)2(CH3OH)2]·4CH3OH (1) and [Cd4(L)2(η-OAc)2(CH3OH)2] (2) have been constructed successfully applying the measure of solvent evaporation and characterized structurally by X-ray diffraction analyses of single crystal, IR & UV visible analyses. The single crystals of the salamo-like oligo(N,O-donor) compound H3L have been obtained by wet-chemical technique, its established structure is H3L∙CH3OH. The structure of complex 1 is centrally symmetrical, and both Mn(III) atoms are hexa-coordination and have slightly distorted octahedral geometries. There are two sets of intermolecular H-bonding interactions which are connected with adjacent units of the Mn(III) complexes and form a two-dimensional network structure. For the complex 2, all of the Cd(II) atoms are also hexa-coordination and possess slightly twisted octahedral configurations. And five groups of intermolecular H-bonding interactions form a honeycomb shaped three-dimensional supramolecular structure. Additionally, the intermolecular interactions of H3L, complexes 1 and 2 have been quantified by Hirshfeld surface analysis for further study. Fluorescence emission spectra of H3L, complexes 1 and 2 were also investigated.

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