6533b7d1fe1ef96bd125d8b0

RESEARCH PRODUCT

Coordination versatility of pyridine-functionalized N-heterocyclic carbenes: a detailed study of the different activation procedures. Characterization of new Rh and Ir compounds and study of their catalytic activity.

Elena Mas-marzáEduardo PerisMercedes Sanaú

subject

chemistry.chemical_classificationHydrosilylationSalt (chemistry)Hydrogen transferCrystal structureMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compoundTransmetalationDeprotonationchemistryPyridineOrganic chemistryPhysical and Theoretical Chemistry

description

Three different reaction procedures for the coordination of N-n-butyl-N'-(2-pyridylmethyl)imidazolium salt have produced new N-heterocyclic complexes of Rh and Ir. The direct reaction of the imidazolium salt with [IrCl(cod)](2) provides a NHC-Ir(III)-H complex, while transmetalation from a silver-NHC complex and deprotonation with NEt(3) give new NHC complexes of M(I) and M(III) when reacting with [MCl(cod)](2) or [MCl(coe)(2)](2) (M = Rh, Ir). The crystal structures of the biscarbene Rh(III) and Ir(III) complexes are described. The catalytic properties of the compounds obtained have been tested in the hydrosilylation of acetylenes, the cyclization of acetylenic carboxylic acids, and hydrogen transfer to ketones.

10.1021/ic051272bhttps://pubmed.ncbi.nlm.nih.gov/16363868