6533b835fe1ef96bd129e98d

RESEARCH PRODUCT

2D and 3D coordination polymers based on 2,2′-bipyrimidine and cyanide bridging ligands incorporating coordinated and guest ammonia molecules. Synthesis, crystal structures, magnetic properties and thermal analysis of {[Ni(CN)4]2[(Ni(NH3)2)2(bpym)]·2H2O}n and {[Cu2(CN)2(bpym)]·NH3}n

Enrique ColacioAntonio RomerosaJosé Suárez-varelaHelen Stoeckli-evansFrancesc LloretMiguel Navarrete

subject

Aqueous solutionHydrogen bondChemistryCyanideInorganic chemistryGeneral ChemistryCrystal structureCatalysisIonCrystallographychemistry.chemical_compoundOctahedronMaterials ChemistryAntiferromagnetismMolecule

description

The coordination polymers {[Ni(CN)4]2[(Ni(NH3)2)2(bpym)]·2H2O}n1 and {[Cu2(CN)2(bpym)]·NH3}n2 have been prepared from the reactions of M(NO3)2·nH2O [Cu(II), n = 3 and M = Ni(II), n = 6] with NaCN and bpym (2,2′-bipyrimidine) in concentrated aqueous ammonia, respectively. The structure of 1 is made of bipyrimidine bridged centrosymmetric dinuclear [Ni(NH3)2(μ-bpym)Ni(NH3)2] fragments connected by four [Ni(CN)4]2− anions giving rise to a 2D framework. Layers, which adopt a stair-like conformation, are stacked with an ABAB… repeat pattern. Water molecules are located in the interlayer space and are involved in hydrogen bond interactions with the non-bridging cyanide groups of the [Ni(CN)4]2− anions and one of the ammonia molecules. Magnetic measurements clearly show the existence of antiferromagnetic exchange interactions between the local spin triplet states of the octahedral Ni(II) ions mainly mediated by the bpym exchange pathway with a J value of −16.82 cm−1. The structure of 2 consists of [Cu2(bpym)] centrosymmetric fragments connected by cyanide groups to four neighbouring Cu(I) ions giving rise to a 3D network with channels perpendicular to the bc plane. Guest ammonia molecules are located into channels. TG-XRD combined studies show that the structure of 1 is retained after dehydration whereas that of 2, however, collapses after ammonia elimination.

https://doi.org/10.1039/b507136d