We demonstrate the breakdown of molecular-frame dynamics induced by the
uncoupling of molecular rotation from electronic motion in molecular Rydberg
states. We observe this non-Born-Oppenheimer regime in the time domain through
photoelectron imaging of a coherent molecular Rydberg wave packet in
N2. The photoelectron angular distribution shows a radically
different time evolution than that of a typical molecular-frame-fixed electron
orbital, revealing the uncoupled motion of the electron as it precesses around
the averaged anisotropic potential of the rotating ion-core.Comment: 6 pages, 4 figure