Catalytically active palladium pyridylidene complexes: pyridinium ionic liquids as N-heterocyclic carbene precursors

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منابع مشابه

Catalytically active palladium pyridylidene complexes: pyridinium ionic liquids as N-heterocyclic carbene precursors.

Pyridinium salts similar to those used as ionic liquid solvents readily undergo palladation in the presence of a base, thus giving palladium-pyridylidene N-heterocyclic carbene complexes that are active catalysts for Suzuki-type cross-coupling reactions.

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The transamination of alkyl-palladium halide N-heterocyclic carbene complexes has enabled the isolation of products that reveal interesting insights into the factors which might be barriers to the development of a palladium-catalysed alkyl-amination reaction.

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N-heterocyclic carbene tethered amido complexes of palladium and platinum.

With a view to applications in bifunctional catalysis, a modular cross-coupling strategy has been used to prepare amine bis(imidazolium) salts (3a and 3b) and an amine mono(imidazolium) salt (6) as precursors to chelating amido-NHC ligands. Treating the pro-ligands 3 with 3 equivalents of the bulky base KHMDS and Pd(OAc)(2) or PtCl(2)(COD) gave the four amido bis(N-heterocyclic carbene) pincer ...

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Carbene-anchored/pendent-imidazolium species as precursors to di-N-heterocyclic carbene-bridged mixed-metal complexes.

Reaction of a series of linked diimidazolium dibromide salts with one-half equivalent of [Rh(mu-OAc)(COD)](2) under reflux conditions generates a series of carbene-anchored/pendent-imidazolium complexes, [RhBr(COD)((R)C(H)-eta(1)-C(eth))][Br] ((Me)C(H)-eta(1)-C(eth) = ethylene[(N-methyl)imidazolium][(N-methyl)imidazole-2-ylidene] and (tBu)C(H)-eta(1)-C(eth) = ethylene[(N-tert-butyl)imidazolium]...

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A method is described that makes use of easily prepared, inexpensive copper synthons as N-heterocyclic carbene (NHC) transfer agents to generate catalytically relevant gold and palladium complexes.

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ژورنال

عنوان ژورنال: Chemical Communications

سال: 2005

ISSN: 1359-7345,1364-548X

DOI: 10.1039/b508225k