Quasibound rovibronic states in CO+ and NO+ with excitation energies o
f more than 20 eV are formed in charge-exchange reactions of CO2+ and
NO2+ with alkali atoms. The kinetic energy released upon dissociation
is measured by using translational spectroscopy. A new and simple devi
ce is presented to determine which fragment holds the charge. A large
number of quasibound states is found, spread over all dissociation lim
its. The complexity of the spectra prevents a full interpretation of a
ll structures. The absence of long-lived vibrationally excited states
in CO2+, which was predicted theoretically, is corroborated.