Tetracyanidopalladates of Cu(II) with 2-aminoethylpyridines as blocking ligands: The role of the 2-aminoethyl arm position on the pyridine ring.

Three novel Cu(II) compounds Cu(2aepy)Pd(CN)4 (1), cu(3aepy)Pd(CN)4H20 (2) and [Cu(4aepy)2(F120)21 [Pd(CN)41 (3) (Xaepy = X(2-aminoethylpyridine), X = 2,3,4) were isolated in single crystal form from the aqueous systems Cu2 – Xaepy – [Pd(CN)4]2-. The resulting crystal structures depend on the position of 2-aminoethyl arm on the pyridine ring: 1 exhibits a three-dimensional (3d) polymeric structure and only one chelating 2aepy ligand is ligated to the pentacoordinated Cu(II) atom ( = 50%); the crystal structure of 2 features a puckered 2d polymer formed by hexacoordinated Cu(II) atoms (4 + I + 1 form) and [Pd(CN)4]2- anions linked by bridging cyanido ligands; and the Cu(II) atoms are additionally bridged by 3aepy ligands. The crystal structure of 3 is built up of positively charged chains in which [Cu(H20)212+ fragments are linked by a pair of 4aepy ligands, giving hexacoordinated Cu(II) in the 4 + 2 form, with (Pd(CN)4]2- counter anions. Hydrogen bonds reinforce the crystal structures of 1-3. Variable temperature magnetic studies based on susceptibility and magnetization measurements down to 2 K reveal that 1 deviates from Curie-Weiss behavior at low temperature, while 2 and 3 exhibit Curie-Weiss behavior with 0 values of 0.85 K and 0.46 K for 2 and 3, respectively. (C) 2014 Elsevier B.V. All rights reserved.