{(COD)Ru[RN=C(H)-C(H)=C(Ph)]₂} (R = Me, Et): The first structurally characterized mononuclear ruthenium complexes with enyl-imino ligands and their relevance in ruthenium catalyzed C-H activation reactions
Journal of Organometallic Chemistry. Bd. 695. H. 18. Amsterdam: Elsevier 2010 S. 2076 - 2082
Erscheinungsjahr: 2010
ISBN/ISSN: 1872-8561
Publikationstyp: Zeitschriftenaufsatz
Sprache: Englisch
Doi/URN: 10.1016/j.jorganchem.2010.05.020
Geprüft | Bibliothek |
Inhaltszusammenfassung
The reaction of alpha,beta-unsaturated imines with [(1,5-cyclooctadiene)-bis(2-methylallyl)-ruthenium(II)] leads to the formation of mononuclear ruthenium complexes of the general formula {(COD)Ru[RN=C (H)-C(H)=C(Ph)](2)}. In these complexes the imine ligands are deprotonated in beta-position with respect to the imine double bond and coordinate as an enyl-imino ligand. In the case of R = Me, Et the corresponding compounds have been characterized by X-ray crystallography. The relevance of thes...The reaction of alpha,beta-unsaturated imines with [(1,5-cyclooctadiene)-bis(2-methylallyl)-ruthenium(II)] leads to the formation of mononuclear ruthenium complexes of the general formula {(COD)Ru[RN=C (H)-C(H)=C(Ph)](2)}. In these complexes the imine ligands are deprotonated in beta-position with respect to the imine double bond and coordinate as an enyl-imino ligand. In the case of R = Me, Et the corresponding compounds have been characterized by X-ray crystallography. The relevance of these complexes with respect to ruthenium catalyzed C-C coupling reactions of the same alpha,beta-unsaturated imines is demonstrated by the structural analysis of another mononuclear ruthenium complex in which two imine ligands are reductively coupled (R = Cy). [(1,5-Cyclooctadiene)-bis(2-methylallyl)-ruthenium (II)] also turns out to be a highly effective precatalyst in the reaction of the respective imines with carbon monoxide and ethylene to produce heterocyclic compounds. (c) 2010 Elsevier B.V. All rights reserved. » weiterlesen» einklappen