Abstract
The understanding of fundamental atomic-level processes often requires well-defined model systems. The oxygen atom transfer from CO(2) to a transition metal cation in the gas phase presents such a model system. We investigate the reaction of Ta(+) + CO(2) for which the formation of TaO(+) is highly efficient and attributed to multistate reactivity. Here, we study the atomistic dynamics of the oxygen atom transfer reaction by recording experimental energy and angle differential cross sections by crossed beam velocity map imaging supported by ab initio quantum chemical calculations. Product ion velocity distributions are dominated by signatures for indirect dynamics, despite the reaction being highly exothermic. Product kinetic energy distributions show little dependence on additional collision energy even with only four atoms involved, which hints at dynamical trapping behind a submerged barrier.