Nitric oxide is vibrationally excited in a flowing gas mixture of NO-A
r using resonance absorption of single-line CO laser radiation. The fl
uorescence in the infrared and in the ultraviolet is analyzed under st
eady-state pumping conditions. Quantitative analysis of the NO IR over
tone spectrum, DELTAupsilon=2, allows inference of the vibrational dis
tribution function of the X 2PI ground state up to vibrational level u
psilon=15. It is shown that the mechanism of vibrational excitation is
anharmonic vibration-vibration pumping. In particular, the higher vib
rational levels, upsilon greater-than-or-equal-to 8, are populated by
near-resonant vibration-to-vibration exchange processes. It is suggest
ed that the electronically excited NO molecules in A 2SIGMA and B 2PI
States, which are observed, can be produced both by resonant vibration
-to-electronic energy transfer processes and in energy pooling reactio
ns. Previous rate measurement experiments in NO are analyzed and discu
ssed in light of the present data, and further state-resolved measurem
ents are proposed.