Abstract

The self-assembly between a chiral polydentate N8O4 ligand, containing a bis-imidazole unit substituted by 4 l-valine groups, and copper(II) ions leads to an optically pure, infinite M-helical chain. The X-ray diffraction studies revealed that the compound crystallizes in the hexagonal chiral space group P6122 with a single [HValbiim]5− unit coordinating three different copper(II) centers. Cu1 is in a distorted square-pyramidal environment, Cu2 is involved as well in a five-coordinated CuN2O3 chromophore but with a coordination geometry intermediate between a square pyramid and a trigonal bipyramid, and the third copper(II) ion, namely, Cu3, is in a slightly distorted square planar environment defined by three nitrogen atoms and one oxygen atom from two [HValbiim]5− ligands. The resulting double bridge (namely, Cu2−O42′′ and Cu2′′−O42) gives rise to the formation of a hexanuclear entity. The found antiferromagnetic behavior, successfully modeled by an isosceles triangle, is consistent with the strong coup...

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