Synthesis, crystal structure, and magnetic properties of oxalato-copper(II) complexes with 3,3-bis(2-imidazolyl)propionic acid, an imidazole-carboxylate polyfunctional ligand:: From mononuclear entities to ladder-like chains

The synthesis of five new Cu(II) compounds of formula [Cu(HBIP)(C2O4)]. H2O (1), [Cu(HBIP)(C2O4)(OH2)]. 2H(2)O (2), [{Cu(HBIP)Cl}(2)(mu-C2O4)]. 2H(2)O (3), [{Cu(BIP)}(2)(mu-C2O4)]. 2H(2)O (4) and [{Cu(BIP)}(2)(mu-C2O4)]. 6H(2)O (5), together with their spectral and magnetic characterization, is reported. Crystal structures of compounds 2, 3 and 5 have been solved. All these compounds crystallize in the triclinic system, space group P (1) over bar, with a = 7.3322(3) Angstrom, b = 10.014(1) Angstrom, c = 11.541(1) Angstrom, alpha = 113.22(1)degrees, beta = 91.37(1)degrees, gamma = 94.51(1)degrees, Z = 2 for compound 2; a = 7.444(2) Angstrom, b = 8.518(2) Angstrom, c = 11.231(2) Angstrom, alpha = 97.45(2)degrees, beta = 98.99(2)degrees, gamma = 97.95(2)degrees, Z = 1 for compound 3; and a = 7.977(1) Angstrom, b = 8.656(1) Angstrom, c = 11.807(11) Angstrom, alpha = 69.06(1)degrees, beta = 86.07(1)degrees, gamma = 67.36(1)degrees, Z = 1 for compound 5. In compound 2 the asymmetric unit consists of one isolated neutral [Cu(HBIP)(C2O4)(OH2)] molecule and two noncoordinated water molecules. The Cu(II) ion is five-coordinated (4+1 coordination mode) with HBIP and oxalato entities acting as bidentate ligands and the water molecule as the fifth ligand. The structure off compound 3 is made up of centrosymmetric binuclear [{Cu(HBIP)(Cl)}(2)(mu-C2O4)] units and noncoordinated water molecules. The two copper atoms are linked through a bis-bidentate oxalato group leading to a metal-metal separation of 5.28(3) Angstrom. The coordination stereochemistry of the CuN2O2Cl chromophore is approximately SP. Compound 5 exhibits a structure built of ladder-like chains. In these chains the rungs are constituted by the neutral dinuclear centrosymmetric [(BIP)Cu(C2O4)Cu(BIP)] entities. The oxalato group bridges two copper atoms in a bis-bidentate fashion, whereas the BIP acts as a tridentate ligand, connecting through their carboxylate groups these dimeric units along the a axis. The copper atom is involved in a five-coordinated CuN2O2O' chromophore, with a coordination geometry intermediate between SP and TBP. The magnetic properties of all complexes have been investigated. Compound 1 and 2 follow a Curie-Weiss law with very low values of theta. The other three compounds exhibit an antiferromagnetic coupling, with 2J = -265 cm(-1) for 3, 2J = -108 cm(-1) for 4, and 2J = -5.7 cm(-1) for 5. The strength of the exchange interaction is discussed on the basis of the structural features and correlated with published magneto-structural data on similar oxalato-bridged copper(II) compounds.