Jc. Owrutsky et Ap. Baronavski, TIME-RESOLVED MULTIPHOTON IONIZATION STUDY OF THE 102 NM STATE OF NO, The Journal of chemical physics, 101(7), 1994, pp. 5708-5716
We have used subpicosecond deep UV laser pulses (near 205 nm) in a tim
e-resolved (2+1) multiphoton ionization study of the two-photon state
of NO at 102 nm via a one-photon resonance with the A (2) Sigma(+) (3s
sigma) (v=2) state. The two-photon excited state lifetime exhibits a
strong pressure dependence from which the collisionless lifetime and t
he bimolecular depopulation or quenching rate constant were obtained.
The large quenching rate constant strongly suggests that the state is
a medium (10-12) n Rydberg level in the series converging to the groun
d electronic state of NO+. The subnanosecond collisionless lifetime im
plies that this state is subject to predissociation and/or autoionizat
ion.