Confinement-Induced Selectivities in Gold(I) Catalysis-The Benefit of Using Bulky Tri-(ortho-biaryl)phosphine Ligands
Karim Muratov1, Fabien Gagosz1
1Department of Chemistry and Biomolecular Sciences, University of Ottawa, K1N 6N5, Ottawa, Canada.
Abstract:
The confinement of a catalytic site is an efficient strategy to control a reaction and modulate its selectivity. In the present work, a new class of structurally simple and easily accessible bulky tri-(ortho-biaryl)phosphine ligands were accessed, and their gold(I) complexes synthesized. Their X-ray diffraction analysis and the comparative evaluation of their VBur % and G steric parameters against a series of gold complexes commonly employed in catalysis demonstrated their confined nature. Despite their notable steric congestion, these complexes exhibited remarkable catalytic activities and unusual selectivities, both in nature and level, that make them unique in the field of synthetic homogeneous gold catalysis.
More Related Videos
![Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F51444.jpg&w=3840&q=50)
11:44Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions
Published on: March 20, 2014
07:14Author Spotlight: Experimental Approaches for the Synthesis of Low-Valent Metal-Organic Frameworks from Multitopic Phosphine Linkers
Published on: May 12, 2023
Related Concept Videos
02:51Metal-Ligand Bonds
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
02:36Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn...
02:17Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
01:19Complexation Equilibria: The Chelate Effect
01:11ortho–para-Directing Activators: –CH3, –OH, –NH2, –OCH3