The reactivity of bulk NO clusters produced by plasma oxidation of Pd(100) towards propene, oxidation was characterized using temperature programmed desorption (TPD) and isothermal oxygen titration. The TPD results were dominated by simultaneous CO2 and water desorption in a peak at 490 K. The only other product observed was a small amount of CO near saturation propene coverages that also desorbed at 490 K. The propene coverage saturated at exposures between 0.5-1 1, indicating a sticking coefficient close to one. In the titration experiments, CO2 production peaked almost immediately upon exposure to propene, indicating that the propene oxidation rate fell as the surface was reduced. Above 450 K, virtually all of the propene was completely oxidized to CO2 and water, while at lower temperatures small amounts of CO were observed and unreacted propene fragments accumulated on the surface. In comparison, previous results for a well-ordered surface oxide on Pd(100) were similar in that CO2 and water also desorbed simultaneously indicating a similar mechanism, but different in that the sticking coefficient on the surface oxide was a factor of 20 lower, and the desorption peaked 60 K lower. These differences cause the bulk oxide to be far more active at higher temperatures than the surface oxide, but the surface oxide displays some activity down to lower temperatures where propene simply accumulates on the bulk oxide surface. (c) 2007 Elsevier Inc. All rights reserved.