Canadian Journal of Chemistry · 1992 · 37 citations · 0 references
Natural SciencesChemistryMaterials ScienceInorganic ChemistryMaterials ChemistryPolymer ChemistryCoordination ChemistryCoordination PolymersMetal MaterialsMetal-ligand BondingTransition Metal ChemistryTransition Metal ComplexesCoordination Polymer SynthesisElectronic Spectra Of Transition Metal ComplexesElectronic Structure Of Metal ComplexesInfrared Spectroscopic AnalysisMagnetic Properties Of Transition Metal ComplexesMagnetic Susceptibility AnalysisMetal-ligand Coordination PolymersSolubility
The copper(I) complexes [Cu(4-Xdmpz)] 3 (where X = H, Cl, Br, I and CH 3 ; dmpz = 3,5-dimethylpyrazolate) and the copper(II) complexes [Cu(4-Xdmpz) 2 ] x have been synthesized and characterized. Qualitative solubility, infrared spectroscopic, and differential scanning calorimetric studies are reported for all complexes. Mass spectra support trimeric formulations for the copper(I) complexes. Scanning electron micrographs and powder X-ray diffractograms have been recorded for the copper(II) compounds. Electronic and EPR spectroscopic studies as well as magnetic susceptibility studies from 2 to 300 K are also reported for the copper(II) compounds, which are proposed to have polymeric chain structures. The magnetic data reveal strong antiferromagnetic interactions in all four of the copper(II) compounds. The data have been analysed employing an isotropic Heisenberg model for antiferromagnetic coupling in extended chain polymers. Values of the exchange coupling constant, J, are determined as −58, −61, −66, and −66 cm −1 for the X = H, CH 3 , Cl, and Br complexes respectively. The X = Cl compound exhibits an abrupt decrease in magnetic susceptibility below 40 K and possible causes of this anomalous behaviour are discussed.