Abstract
Diaurated intermediates of gold-catalysed reactions have been a long-standing subject of debate. Although diaurated complexes were regarded as a drain of active monoaurated intermediates in catalytic cycles, they were also identified as the products of gold-gold cooperation in dual-activation reactions.
This study shows investigation of intermediates in water addition to alkynes catalysed by [(IPr)Au(CH3CN)(BF4)]. Electrospray ionisation mass spectrometry (ESI-MS) allowed us to detect both monoaurated and diaurated complexes in this reaction.
Infrared photodissociation spectra of the trapped complexes show that the structure of the intermediates corresponds to alpha-gold ketone intermediates protonated or aurated at the oxygen atom. Delayed reactant labelling experiments provided the half life of the intermediates in reaction of 1-phenylpropyne (similar to 7 min) and the kinetic isotope effects for hydrogen introduction to the carbon atom (KIE similar to 4-6) and for the protodeauration (KIE similar to 2).
The results suggest that the ESI-MS detected monoaurated and diaurated complexes report on species with a very similar or the same kinetics in solution. Kinetic analysis of the overall reaction showed that the reaction rate is first-order dependent on the concentration of the gold catalyst.
Finally, all results are consistent with the reaction mechanism proceeding via monoaurated neutral alpha-gold ketone intermediates only.