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- Title
Remarkable Ability of the Benzylidene Ligand To Control Initiation of Hoveyda-Grubbs Metathesis Catalysts.
- Authors
Basak, Tymoteusz; Grudzień, Krzysztof; Barbasiewicz, Michał
- Abstract
The structure of the chelating benzylidene ligand offers the unique ability to control the initiation of Hoveyda-Grubbs metathesis catalysts. Apart from steric and electronic effects acting on the step involving opening of the chelate ring, changes related to the following ligand-exchange process may also play a critical role. Our mechanistic model reveals that ligands substituted at the 6-position of the benzylidene ring enter the metathesis cycle in a nonoptimal chelating conformation, and thus the coordination number of the ruthenium center transiently increases to six (associative mechanism). In effect, the synthesis and initiation of the catalysts becomes difficult, and the energy barrier of the ligand-exchange process is controlled by the structure of the coordinating OR group. Moreover, we explain how isomeric naphthalene ligands affect the catalytic performance by an indivisible combination of steric and π-electron delocalization effects.
- Subjects
RADIOENZYMATIC assays; BENZYLIDENE compounds; CATALYSIS; ACTIVATION energy; ELECTRON delocalization
- Publication
European Journal of Inorganic Chemistry, 2016, Vol 2016, Issue 21, p3513
- ISSN
1434-1948
- Publication type
Article
- DOI
10.1002/ejic.201600435