Femtosecond time-resolved photoelectron angular distributions (PADs) are me
asured for the first time in the molecular frame of a dissociating molecule
. Various stages of the dissociation process, NO2 --> NO((CII)-I-2) + O(P-3
), are probed using ionization of the NO((CII)-I-2) fragment to NO+(X(1)Sig
ma(+)). The PADs evolve from forward-backward asymmetric with respect to th
e dissociation axis at short time delays (less than or equal to 500 fs) to
symmetric at long time delays (greater than or equal to 1 ps). Changes in t
he PADs directly reflect the time dependent separation and reorientation of
the dissociating photofragments.