Cu(bapen)M(CN)4·H2O complexes exhibiting chain-like structures (bapen = N,N′-bis(3-aminopropyl)-1,2-diaminoethane, M = Ni, Pd): preparations, crystal structures, spectroscopic and magnetic properties

El pdf del artículo es la versión post-print.-- et al.Single crystals of Cu(bapen)Ni(CN)4·H2O and Cu(bapen)Pd(CN)4·H2O (bapen = N,N′-bis(3-aminopropyl)-1,2-diaminoethane) were isolated from the aqueous systems copper(II)—bapen—[M(CN)4]2− (M = Ni, Pd). Crystals of the two compounds are isostructural and are built up of two crystallographically independent quasi-linear chains [-Cu(bapen)-μ2-NC-Ni(CN)2-μ2-CN-] n and solvate water molecules. The copper(II) centers exhibit the usual distorted octahedral coordination with one tetradentate bapen ligand in the equatorial plane (mean Cu–N are 2.030 Å for Cu(bapen)Ni(CN)4·H2O and 2.018 Å for Cu(bapen)Pd(CN)4·H2O), while the axial positions are occupied by nitrogen atoms from μ2-bridging cyanido ligands with longer Cu–N bonds (mean values are 2.544 Å for Cu(bapen)Ni(CN)4·H2O and 2.543 Å for Cu(bapen)Pd(CN)4·H2O). One of the two independent coordinated bapen ligands is disordered, as are the water molecules of crystallization. The Ni and Pd atoms in both studied compounds exhibit the usual square coordination with the bridging cyanido ligands trans to each other. Several OH···O, N–H···O and N–H···N hydrogen bonds enhance the stability of the structures. ESR spectra corroborated the presence of Jahn–Teller anisotropy at the copper(II) atoms. Magnetic studies in the temperature range 1.8–300 K reveal that both Cu(bapen)Ni(CN)4·H2O and Cu(bapen)Pd(CN)4·H2O follow Curie-Weiss laws with θ = −0.51 K and θ = −0.34 K, respectively, suggesting the presence of weak antiferromagnetic interactions.This work was supported by the Slovak grant VEGA (grant no. 1/0089/09), VVGS PF 22/2011Ch, and by SAS Centre of Excellence: CFNT MVEP. Funding from the Ministry of Science and Innovation (Spain) under grants MAT2011-27233-C02-1 and CONSOLIDER 25200, and from the Diputación General de Aragón is gratefully acknowledged.Peer Reviewe