Scinovex
articleTop 1% cited

Palladium Complexes with Tridentate Pincer Bis-Carbene Ligands as Efficient Catalysts for C−C Coupling

Organometallics · 2002 · Vol. 21(4) · pp. 700–706
Jennifer A. LochMartin AlbrechtEduardo PerisJ.A. MataJ.W. FallerRobert H. Crabtree

Abstract

The synthesis and X-ray crystallographic characterization of a Pd complex (3) with a rigid C,N,C-tridentate pincer carbene ligand are described. At high temperatures (165 °C) it is an active and robust catalyst in the Heck reaction. Complex 3 gives some of the highest turnover numbers yet reported for coupling with aryl chlorides. Time dependence, reuse, and Heck reaction conditions are discussed for 3. Data with F- as base did not support Shaw's Heck mechanism. Suzuki and Sonogashira coupling reactions are also catalyzed by 3. The palladium carbene complex 5, containing an analogous C,N-bidentate ligand, is compared to 3 in terms of stability, catalytic activity, and reaction profile in the Heck reaction.

Catalytic Cross-Coupling ReactionsCatalytic C–H Functionalization MethodsN-Heterocyclic Carbenes in Organic and Inorganic ChemistryChemistryCarbenePincer movementSonogashira couplingHeck reactionCatalysisPalladiumArylLigand (biochemistry)Denticity
Citations
362
FWCI
23.97
field-weighted impact
References
22
Percentile
100%
vs. same field & year
Citations per year
References
Chelating N-heterocyclic carbene ligands in palladium-catalyzed heck-type reactions
Journal of Organometallic Chemistry · 1998 · 526 citations
The Heck Reaction as a Sharpening Stone of Palladium Catalysis
Chemical Reviews · 2000 · 3,857 citations
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.