Halogen Bond Activation in Gold Catalysis

Gold catalysis has, over the past decades, provided innovative organic transformations under mild conditions with high chemoselectivities. It receives steadily growing attention thanks to its wide synthetic applicability. The catalytically active form, [L-n-Au](+), of ligated gold complexes, [L-n-Au-Cl], is formed via halide abstraction. This is typically achieved by anion exchange upon the addition of an appropriate silver salt to the reaction mixture. Herein, an alternative silver-free route for gold activation is presented, making use of halogen bonding to promote halide abstraction. We demonstrate that a catalytic amount of a strong halogen bond donor efficiently activates both gold(I) and gold(III) catalysts. Following the reaction, both the catalyst and the activator are easily recovered. Importantly, this not only reduces the metal waste in a gold-catalyzed process but also enables its upscaling, possibly opening new avenues for its use in industrial settings. Gold is an expensive and limited resource, and its recyclability is of supreme importance. Based on systematic reaction kinetics, NMR spectroscopic, and computational investigations, we describe the mechanism of halogen bond-activated goId(I/III) catalysis using cyclopropanation as a model reaction. Our discovery paves the way for the development of gold-mediated transformations that allow recycling of the precious gold catalyst and that may thereby become useful also for the large-scale generation of complex molecules.

Automated summary

Gold catalysis provides innovative organic transformations with high chemoselectivity under mild conditions. A silver-free route utilizing halogen bonding is presented for gold activation, reducing metal waste and enabling large-scale generation of complex molecules. The recyclability of gold is of supreme importance.