Organometallics · 2002 · 82 citations · 81 references
Natural SciencesChemistryInorganic ChemistryOrganic ChemistryQuantum ChemistryCarbene ComplexesChemical BondingCoordination ChemistryMetal-ligand BondingMolecular BondingTransition Metal ComplexesCarbene Complex ReactivityCarbene Coordination ChemistryElectronic Structure Of Carbene ComplexesFischer Carbene ComplexesLigand Electronic EffectsMetal-carbene BondingSubstituent Electronic ParametersTransition Metal Carbene Complexes
In this work we have examined a series of 25 different Fischer carbene complexes of the type (CO) 5 Cr C(X)R with X = H, OH, OCH 3, NH 2, and NHCH 3 and R = H, CH 3, CH CH 2, Ph, and C⋮CH, to analyze the influence of each substituent on the molecular structure and bonding of these complexes. Energy and charge decomposition analysis of the interaction between the chromium pentacarbonyl and the carbene fragments reveal that for the metal−carbene bond donation is quantitatively more important than back-donation. However, it is the back-donation rather than donation that correlates with most geometrical and electronic parameters of the complexes studied. The reasons for the larger influence of back-donation on the molecular structure of Fischer carbene complexes are discussed.
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Density-functional theory of atoms and molecules
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