Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
37
pubmed:dateCreated
2009-9-21
pubmed:abstractText
Sterically similar palladium dicarbene complexes have been synthesized that comprise permethylated dicarbene ligands which bind the metal center either in a normal coordination mode via C2 or abnormally via C4. Due to the strong structural analogy of the complexes, differences in reactivity patterns may be attributed to the distinct electronic impact of normal versus abnormal carbene bonding, while stereoelectronic effects are negligible. Unique reactivity patterns have been identified for the abnormal carbene complexes, specifically upon reaction with Lewis acids and in oxidative addition-reductive elimination sequences. These reactivities as well as analytical investigations using X-ray diffraction and X-ray photoelectron spectroscopy indicate that the C4 bonding mode increases the electron density at the metal center substantially, classifying such C4-bound carbene ligands amongst the most basic neutral donors known thus far. A direct application of this enhanced electron density at the metal center is demonstrated by the catalytic H(2) activation with abnormal carbene complexes under mild conditions, leading to a catalytic process for the hydrogenation of olefins.
pubmed:language
eng
pubmed:journal
pubmed:status
PubMed-not-MEDLINE
pubmed:month
Sep
pubmed:issn
1521-3765
pubmed:author
pubmed:issnType
Electronic
pubmed:day
21
pubmed:volume
15
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
9375-86
pubmed:year
2009
pubmed:articleTitle
On the electronic impact of abnormal C4-bonding in N-heterocyclic carbene complexes.
pubmed:affiliation
Department of Chemistry, University of Fribourg, Chemin du Musée 9, 1700 Fribourg, Switzerland.
pubmed:publicationType
Journal Article