Chemistry - A European Journal · 2013 · 17 citations · 63 references
Natural SciencesChemistryInorganic ChemistryOrganic ChemistryOrganometallic ChemistryCarbene ComplexesCoordination ChemistryHeterocyclic ChemistryHeterocyclic CompoundsMolecular StructureMolecular SymmetryCarbene Complex SynthesisCarbene Coordination ChemistryCoordination Geometry DeterminationRing StructureStereochemical Analysis By Nuclear Magnetic Resonance SpectroscopyStereochemical ModificationSubstituent Effects On Ring Conformation
Palladium and platinum complexes containing a sulfur-functionalised N-heterocyclic carbene (S-NHC) chelate ligand have been synthesised. The absolute conformations of these novel organometallic S-NHC chelates were determined by X-ray structural analyses and solution-phase 2D (1)H-(1)H ROESY NMR spectroscopy. The structural studies revealed that the phenyl substituents on the stereogenic carbon atoms invariably take up the axial positions on the Pd-C-S coordination plane to afford a skewed five-membered ring structure. All of the chiral complexes are structurally rigid and stereochemically locked in a chiral ring conformation that is either (Rs ,S,R)-λ or (Ss ,R,R)-δ in both the solid state and solution.
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