Abstract
AbstractA combined theoretical and experimental approach has been used to study the unusual mechanism of oxidative addition of aryl iodides to [bipyAu(C2H4)]+complexes. The modular nature of this system allowed a systematic assessment of the effects of complex structure. Computational comparisons between cationic gold and the isolobal (neutral) Pd0and Pt0complexes revealed similar mechanistic features, but with oxidative addition being significantly favored for the group 10 metals. Further differences between Au and Pd were seen in experimental studies: studying reaction rates as a function of electronic and steric properties showed that ligands bearing more electron‐poor functionality increase the rate of oxidative addition; in a complementary way, electron‐rich aryl iodides give faster rates. This divergence in mechanism compared to Pd suggests that Ar−X oxidative addition with Au can underpin a broad range of new or complementary transformations.
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