Ultrafast electron diffraction (UED) is developed, in this and the accompanying paper, as a method for studying
gas-phase molecular structure and dynamics on the picosecond (ps) to femtosecond (fs) time scale. Building
on our earlier reports (henceforth referred to as 1-3), we discuss theoretical and experimental considerations
for the approach. Specifically we show that the use of rotational and vibrational coherences can add a new
dimension to structural determination of gas-phase species. In addition to the internuclear separations of the
molecular sample, the spatial alignment reflected in the scattering pattern contains bond angles and rotational
constants for both excited-state and ground-state species. Vibrational coherence effects are also observable,
and the motion of the wave packet is revealed by the change of the diffraction pattern with time, thus yielding
the molecular dynamics. UED provides the temporal evolution of the reaction coordinate directly and is well-suited
for studies of global structure changes on this time scale. Paper 5 details our experimental studies with
UED and the current time resolution of the apparatus.
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