Zeitschrift für anorganische und allgemeine Chemie · 2003 · 19 citations · 42 references
Natural SciencesChemistryInorganic ChemistryOrganic ChemistrySolid-state ChemistryCoordination ChemistryCoordination PolymersInorganic SynthesisMetal-ligand BondingTransition Metal ChemistryTransition Metal ComplexesComplexation ChemistryCrystal Structure AnalysisCrystal Structure DeterminationLigand DesignTransition Metal-catalyzed SynthesisTransition-metal-catalyzed Functionalization
Abstract Two different types of modified imido and phosphaneiminato ligands are investigated, namely chelate ligands and redox‐functionalised ligands. The first examples of di(organoimido)chromium as well as di(phosphaneiminato)titanium and niobium chelates are described. Furthermore, the first complexes containing redox‐functionalised organoimido ligands are presented, together with the first structurally characterised redox‐functionalised phosphaneiminato complex. Compounds of the type [(RN) 2 M(CH 2 Ph) 2 ] (M = Cr, Mo) are used as catalysts for the (co‐)polymerisation of the polar olefins methyl methacrylate, acrylonitrile and vinyl acetate. A range of X‐ray crystal structure determinations provide clear evidence for the quantum‐chemical result that, similar to organoimido complexes, the potential energy well for the angle at the nitrogen atom is very shallow for phosphaneiminato complexes.
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Olefin metathesis by molybdenum imido alkylidene catalysts
Richard R. Schrock · Tetrahedron · 1999 · 282 citations