Abstract
The synthesis and structural characterization of a series of palladium complexes bearing N-heterocyclic carbenes (NHC) as supporting ligands are described. The reaction of commercially available [Pd(allyl)Cl](2) and isolated or in situ generated NHC leads to monomeric palladium complexes where one NHC is bound to the metal center, as indicated by spectroscopic and single-crystal X-ray diffraction studies. The relative reactivity trend for these complexes as catalysts in aryl amination is discussed in terms of ligand steric properties, which vary as a function of imidazole-nitrogen substituents and perturbation resulting in modulation of ring planarity. The concept of buried volume is used to quantify the steric demand of each NHC in the corresponding complexes.
| Original language | English |
|---|---|
| Pages (from-to) | 1629-1635 |
| Number of pages | 7 |
| Journal | Organometallics |
| Volume | 23 |
| Issue number | 7 |
| DOIs | |
| Publication status | Published - 29 Mar 2004 |
Keywords
- OLEFIN METATHESIS CATALYSTS
- REDUCTIVE ELIMINATION
- OXIDATIVE ADDITION
- HOMOGENEOUS CATALYSIS
- COUPLING REACTIONS
- BOND FORMATION
- PALLADIUM
- REACTIVITY
- AMINATION
- LIGANDS
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