''Bare'' CeO2+ ions can be prepared in the gas phase by consecutive ox
idation of Ce+ with O-2 and NO2. The ability to activate saturated and
unsaturated hydrocarbons is investigated by use of Fourier-transform
ion cyclotron resonance mass spectrometry. In the reactions of CeO2+ w
ith linear and branched alkanes C-H bond activation is observed almost
exclusively. In contrast, both oxygen-atom transfer and C-H bond acti
vation processes occur when thermalized CeO2+ cations react with simpl
e alkenes and aromatic compounds. C-C bond activation is not observed
at all. Insight into the structural and electronic properties of neutr
al CeO2 and cationic CeO2+ is provided by means of quasirelativistic d
ensity-functional and ab initio pseudopotential calculations. They rev
eal a (2) Sigma(u)(+) ground state for CeO2+ which is best described a
s a linear cerium dioxide with a resonating pi bond. Finally, we discu
ss the influence of oxo ligands on the chemistry of the cationic CeOn (n = 0-2) species toward hydrocarbons.