“…Since the report by Haruta et al of exceptionally high activity of supported Au catalysts for low temperature CO oxidation, 1 researchers have been fascinated by the question of what constitutes the active site and the reason for the high activity. Subsequently, reports of these catalysts being active for other reactions emerged, especially if they are coupled with other catalysts, such as water-gas shift, 2 epoxidation of propylene with H 2 and O 2 , 3 epoxidation of propene and butene with O 2 and CO, 4,5 selective oxidation of propane 6 and other molecules. 7 Not surprisingly, the oxidation of CO is the most studied, and it is well established that the catalytic performance is very sensitive to the preparation method, pre-treatment, residual chloride content, and reaction condition.…”