Journal of the Chemical Society Dalton Transactions · 1981 · 43 citations · 0 references
Natural SciencesChemistryPhysicsInorganic ChemistryOrganometallic ChemistrySpectroscopyCoordination ChemistryMetal-ligand BondingMolecular Orbital TheoryMolecular SymmetryTransition Metal ChemistryTransition Metal ComplexesBidentate Ligand BindingElectronic Spectra Of Transition Metal ComplexesElectronic Structure AnalysisElectronic Structure Of Metal ComplexesSpectroscopy Of Transition Metal Complexes
Reactions of SOCl2 or SOBr2 with a range of 20 vanadyl complexes, [VO(L4)]·(L4= quadridentate or two bidentate ligands), yield solutions containing cis- or trans-dihalogen vanadium(IV) complexes [VX2(L4)]. They are characterised by their e.s.r. spectra and in most cases the unpaired electron is in a dx2–y2 orbital. In some cases both cis and trans isomers can be detected and characterised, because of significant differences in e.s.r. parameters. In the case of [VX2(L4)][X = Cl or Br, L4= tropolonate or perfluoropinacolate], the unpaired electron is in a dz2 orbital and the structure is thought to be trigonal prismatic.