Journal of the Chemical Society Dalton Transactions · 1973 · 18 citations · 0 references
Inorganic ChemistryX-band E.s.rEngineeringPhysicsBiochemistryDimeric FormNatural SciencesCoordination ComplexMagnetic ResonanceAxial SymmetryPhysical ChemistryTriplet StateMolecular ComplexQuantum ChemistryChemistrySchiff-base ComplexesMolecular ChemistryInorganic Compound
The X-band e.s.r. spectra due to the copper(II) Schiff-base complexes, namely bis(N-methylsalicylaldiminato)-copper(II), NN′-ethylenebis(salicylideneiminato)copper(II), NN′-phenylenebis(salicylideneiminato)copper(II), NN′-ethylenebis(o-aminobenzylideneiminato)copper(II), and NN′-phenylenebis(o-aminobenzylideneiminato)-copper(II) in chloroform solution at 77 K exhibit low-field lines, which are attributed to ΔMs=±2 transitions within the triplet state due to dimeric forms of these complexes which exist in frozen solution. The salient features of the low-field lines have been satisfactorily accounted for by means of computer simulated spectra based on dipole–dipole coupled pairs of copper(II) ions in dimers with lower than axial symmetry. The results obtained for the internuclear separations of the copper(II) ions are compared with those obtained from crystallographic data.