Rate Acceleration in Olefin Metathesis through a Fluorine−Ruthenium Interaction
- 22 August 2006
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 128 (36) , 11768-11769
- https://doi.org/10.1021/ja064091x
Abstract
The synthesis, structure, and performance of new ruthenium-based olefin metathesis catalysts, featuring fluorinated NHC ligands are presented. The introduction of halogen atoms into the N-heterocyclic carbene ligand profoundly alters the catalytic activity and can afford a more efficient catalyst. Structural investigations suggest that a fluorine−ruthenium interaction is responsible for this increased activity.Keywords
This publication has 9 references indexed in Scilit:
- Quantitative Structure−Activity Relationships of Ruthenium Catalysts for Olefin MetathesisJournal of the American Chemical Society, 2006
- Ag(I) N-Heterocyclic Carbene Complexes: Synthesis, Structure, and ApplicationChemical Reviews, 2005
- Handbook of MetathesisPublished by Wiley ,2003
- Synthesis and Activity of Ruthenium Alkylidene Complexes Coordinated with Phosphine and N-Heterocyclic Carbene LigandsJournal of the American Chemical Society, 2003
- Efficient and Recyclable Monomeric and Dendritic Ru-Based Metathesis CatalystsJournal of the American Chemical Society, 2000
- Synthesis and Activity of a New Generation of Ruthenium-Based Olefin Metathesis Catalysts Coordinated with 1,3-Dimesityl-4,5-dihydroimidazol-2-ylidene LigandsOrganic Letters, 1999
- Synthesis and Applications of RuCl2(CHR‘)(PR3)2: The Influence of the Alkylidene Moiety on Metathesis ActivityJournal of the American Chemical Society, 1996
- A systematic method of promoting an aryl fluoride to coordinate to ruthenium(11)Inorganica Chimica Acta, 1995
- Coordination chemistry of halocarbonsCoordination Chemistry Reviews, 1990