Rare examples of (high spin) Co(ii) complexes with geometrically constrained tetrathioether ligands exhibit a very unusual structural isomerism, switching reversibly between tetrahedral monomers in solution and octahedral chain polymers in the solid; the crystal structures of one polymeric species and a tetrahedral monomer model compound are described. © The Royal Society of Chemistry.

Square planar neutral dimethyl and cationic allyl complexes of palladium with the electronically nonsymmetric diphenylphosphinomethyl- and pyridyl-N-heterocyclic carbene ligands have been synthesized and characterized. The products from the protonation of the dimethyl complexes with 1 equiv of acid at low temperatures are monomethyl cations, the exact nature of which is dependent on the type of ligand; in pyridine-carbene complexes the Pd-Me bond cleaved is trans to the carbene, while for the phosphino-carbene complexes it is trans to the phosphine. Density functional calculations suggest that protonation in these complexes occurs directly at the methyl ligands and that the site of protonation determines the selectivity of Pd-Me cleavage. For the pyridine-carbene complexes there is a clear preference for protonation trans to the carbene. For phosphino-carbene complexes, however, the site of protonation depends on the steric bulk of the N-heterocyclic carbene ligand. Protonation trans to carbene is favored with small substituents (H, Me), but the bulky 2,6-Pri2C6H3 susbstituent induces protonation trans to the phosphine, as is seen experimentally. © 2007 American Chemical Society.

A study on the Mizoroki-Heck coupling of selected aryl bromides with acrylates catalysed by a series of Pd complexes of bidentate pyridyl-, picolyl-, diphenylphosphinoethyl- and diphenylphosphinomethyl-functionalised N-heterocyclic carbene (NHC) is reported. The observed activity is dependent on the type of solvent and base used and the nature of the "classical" donors of the mixed-donor bidentate ligand and its bite angle. A mechanistic model is presented for the pyridine-functionalised NHC complexes based on an in situ EXAFS study under dilute catalyst conditions (2 mM Pd). The model involves pre-dissociation of the pyridine functionality and oxidative addition of ArBr in the early stages of the reaction, as well as formation of monomeric and dimeric Pd species at the time of substrate conversion. © 2007 Wiley-VCH Verlag GmbH & Co. KGaA.