Answers are grounded in this paper and cite their sources.
[reaction: see text] Ligand-free Pd(OAc)(2) can be used as a catalyst in the Heck reaction of aryl bromides as long as the amount of catalyst is kept between 0.01 and 0.1 mol %. At higher concentrations palladium black forms and the reaction stops. The actual catalyst is monomeric. Palladacycles merely serve as a source of ligand-free palladium in Heck reactions of aryl bromides.
No takes yet. Share an insight, caveat, or question.
Vries et al. (2003) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: