Observations are presented on the

-dependence of rotational relaxation in the CO
200°1 vibrational level for mixtures of CO
2, He, and N
2. The experiment consists of injecting a saturating ∼2-ns pulse at the

line in the 10.4-μ CO
2band into a low-pressure CO
2-laser amplifier while simultaneously monitoring the transient gain response of an overlapping weak probe beam in the 9.4-μ band restricted to operate on any of the transitions

-

. The data show that the decay times of the various

states in the CO
200°1 level get progressively longer for increasing or decreasing

value centered about the perturbed

state. Such behavior may be expected to have a significant effect on the efficiency of energy extraction and pulse shapes in CO
2amplifiers for nanosecond and, especially, subnanosecond laser pulses. An analysis using a coupled set of rate equations to describe the rotational level populations is presented in which consideration is given only to

changes in collision. The analysis, when compared with the data, indicates that collisions in which

changes by more than two units must also be considered.