Crystal Structures of Two Monomeric Copper(II) Carboxylates with 2-Aminopyridine

The crystal structures of two monomeric copper(II) carboxylates with 2-aminopyridine have been determined by X-ray diffraction. The hexanoate complex crystallizes as its acetonitrile solvate Cu(C₆H₁₁O₂)₂(C₅H₆N₂)₂ · CH₃CN] in the triclinic space group P-1 with a = 8.1020(6), b = 13.7106(9), c = 13.7673(9) Å, = 113.79(1), = 103.86(1), and = 94.38(4). The heptanoate compound shows an unsolvated structure Cu(C₇H₁₃O₂)₂(C₅H₆N₂)₂] and also crystallizes in the triclinic space group P-1 with the following cell parameters: a = 8.4487(9), b = 12.238(1), c = 13.504(2) Å, = 87.034(9), = 77.489(9), and = 71.41(1)^°. Both compounds contain the CuO₄N₂ chromophore, with ligands arranged around the copper center in a cis mode. 2-Aminopyridine is coordinated through the endocyclic nitrogen atom. The ortho position of the amino group, with respect to the pyridine nitrogen atom, allows the formation of both, intra-and intermolecular hydrogen bonds.