Ultrafast X-ray scattering offers a structural view of excited-state charge transfer

Intramolecular charge transfer and the associated changes in molecular structure in N,N'-dimethylpiperazine are tracked using femtosecond gas-phase X-ray scattering. The molecules are optically excited to the 3p state at 200 nm. Following rapid relaxation to the 3s state, distinct charge-localized and charge-delocalized species related by charge transfer are observed. The experiment determines the molecular structure of the two species, with the redistribution of electron density accounted for by a scattering correction factor. The initially dominant charge-localized state has a weakened carbon-carbon bond and reorients one methyl group compared with the ground state. Subsequent charge transfer to the charge-delocalized state elongates the carbon-carbon bond further, creating an extended 1.634 Å bond, and also reorients the second methyl group. At the same time, the bond lengths between the nitrogen and the ring-carbon atoms contract from an average of 1.505 to 1.465 Å. The experiment determines the overall charge transfer time constant for approaching the equilibrium between charge-localized and charge-delocalized species to 3.0 ps

Imaging the ring opening reaction of 1,3-cyclohexadiene with MeV ultrafast electron diffraction

We resolve the structural dynamics of the ultrafast photoinduced ring opening reaction of 1,3-cyclohexadiene in space and time employing megaelectronvolt gas phase ultrafast electron diffraction. We, furthermore, observe coherent large amplitude motions of the photoproduct

Determining Orientations of Optical Transition Dipole Moments Using Ultrafast X-ray Scattering

Identification of the initially prepared, optically active state remains a challenging problem in many studies of ultrafast photoinduced processes. We show that the initially excited electronic state can be determined using the anisotropic component of ultrafast time-resolved X-ray scattering signals. The concept is demonstrated using the time-dependent X-ray scattering of <i>N</i>-methyl morpholine in the gas phase upon excitation by a 200 nm linearly polarized optical pulse. Analysis of the angular dependence of the scattering signal near time zero renders the orientation of the transition dipole moment in the molecular frame and identifies the initially excited state as the 3p_<i>z</i> Rydberg state, thus bypassing the need for further experimental studies to determine the starting point of the photoinduced dynamics and clarifying inconsistent computational results

Photoacoustic transients generated by laser irradiation of thin films

Irradiation of an optically thin layer immersed in a transparent fluid with pulsed laser radiation can generate photoacoustic waves through two mechanisms. The first of these is the conventional optical heating of the layer followed by thermal expansion, in which the mechanical motion of the expansion launches a pair of oppositely directed sound waves. A second, recently reported mechanism, is operative when heat is conducted to the transparent medium raising its temperature, while at the same time reducing the temperature in the absorbing body. The latter mechanism has been shown to result in compressive transients at the leading edges of the photoacoustic waveforms. Here the photoacoustic effect produced by irradiating thin metal films which undergo negligible thermal expansion under optical irradiation, but which generate sound solely by the heat transfer mechanism is investigated. Solution to the wave equation for the photoacoustic effect from the heat transfer mechanism is given and compared with the results of experiments using nanosecond laser pulses to irradiate thin metal films