Self-Assembled Molecular Complexes and Coordination Polymers of CdII, Hexamine, and Monocarboxylates: Structural Analysis and Theoretical Studies of Supramolecular Interactions

Abstract

[eng] Four new cadmium(II) complexes [Cd2(bz)4(H2O)4(μ2-hmt)] 3 Hbz 3H2O (1), [Cd3(bz)6(H2O)6(μ2-hmt)2] 3 6H2O (2), [Cd(pa)2(H2O)(μ2-hmt)]n (3), and {[Cd3(ac)6(H2O)3(μ3-hmt)2] 3 6H2O}n (4) with hexamine (hmt) and monocarboxylate ions, benzoate (bz), phenylacetate (pa), or acetate (ac) have been synthesized and characterized structurally. Structure determinations reveal that 1 is dinuclear, 2 is trinuclear, 3 is a one-dimensional (1D) infinite chain, and 4 is a two-dimensional (2D) polymer with fused hexagonal rings consisting of CdII and hmt. All the CdII atoms in the four complexes (except one CdII in 2) possess sevencoordinate pentagonal bipyramidal geometry with the various chelating bidentate carboxylate groups in equatorial sites. One of the CdII ions in 2, a complex that contains two monodentate carboxylates is in a distorted octahedral environment. The bridging mode of hmt is μ2- in complexes 1-3 but is μ3- in complex 4. In all complexes, there are significant numbers of H-bonds,C-H/π, and π-π interactions which play crucial roles in forming the supramolecular networks. The importance of the noncovalent interactions in terms of energies and geometries has been analyzed using high level ab initio calculations. The effect of the cadmium coordinated to hmt on the energetic features of the C-H/π interaction is analyzed. Finally, the interplay between C-H/π and π-π interactions observed in the crystal structure of 3 is also studied.