Reactions of Ru ϩ , Rh ϩ , Pd ϩ , and Ag ϩ with molecular oxygen are studied as a function of kinetic energy by using guided ion beam mass spectrometry. By using a flow tube ion source, it has been possible to create Ru ϩ , Rh ϩ , Pd ϩ , and Ag ϩ ions in their electronic ground state terms and primarily in the lowest spin-orbit levels. All reactions are observed to be endothermic. The reactivity of ground state Ag ϩ is found to be particularly inefficient and is believed to occur through an impulsive pairwise mechanism. Excited states of Ag ϩ are observed to react efficiently at thermal energies. Analyses of the endothermic reaction cross sections yield 0 K bond dissociation energies of D 0 ͑Ru ϩ -O͒ϭ3.81Ϯ0.05 eV, D 0 ͑Rh ϩ -O͒ϭ3.02Ϯ0.06 eV, D 0 ͑Pd ϩ -O͒ϭ1.46Ϯ0.11 eV, and a speculative value of D 0 ͑Ag ϩ -O͒ϭ1.23Ϯ0.05 eV. The reactivity differences among all four metal systems and the electronic states of Ag ϩ are explained by using simple molecular orbital concepts.