The Journal of Chemical Physics · 1967 · 80 citations · 11 references
Natural SciencesChemistryPhysicsComputational ChemistryQuantum ChemistrySpectroscopyAb Initio MethodsDensity Functional TheoryHartree-fock TheoryMetal-ligand BondingMolecular Orbital TheoryTransition Metal ComplexesElectronic Spectra Of Transition Metal ComplexesElectronic Structure AnalysisElectronic Structure Of Metal ComplexesExcitationLigand Electronic EffectsMetal-ligand Bonding AnalysisMolecular Orbital AnalysisSlater-type Orbitals
Charge self-consistent semiempirical calculations including all valence sigma orbitals of the ligands are reported for ferrocene, aminoferrocene, chloroferrocene, and nickelocene. The computations follow the Wolfsberg—Helmholz scheme, and use Slater atomic orbitals which mimic the overlaps, including distance dependence, of the SCF atomic orbitals. An attempt is made to assign electronic excitation energies in a manner consistent with computation and experiment. The only assignment which may be considered reasonably secure is that of the very intense absorption at 51 200 cm−1 which is taken to be the allowed component of the e1g←e1u orbital excitation (fcalc/fobs=0.549/0.691). The ionizing orbital in ferrocene was found to be a1g (−9.78 eV) and in nickelocene was e1g (−6.874 eV). The formal charge on the metal was found to be positive in all cases. A discussion of metal—ligand bonding is included.
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An Extended Hückel Theory. I. Hydrocarbons
Roald Hoffmann · The Journal of Chemical Physics · 1963 · 4.6K citations
J. C. Slater · Physical Review · 1930 · 2.8K citations
A New Type of Organo-Iron Compound
T. J. KEALY, Peter L. Pauson · Nature · 1951 · 1.7K citations