Femtosecond time-resolved electronic relaxation dynamics in tetrathiafulvalene.

In the present paper, the ultrafast electronic relaxation of tetrathiafulvalene (TTF) initiated around 4 eV is studied by femtosecond time-resolved velocity-map imaging. The goal is to investigate the broad double structure observed in the absorption spectrum at this energy. By monitoring the transients of the parent cation and its fragments and by varying the pump and the probe wavelengths, two internal conversions and intramolecular vibrational relaxation are detected both on the order of a few hundred of femtoseconds.

Multi-channel electronic and vibrational dynamics in polyatomic resonant high-order harmonic generation.

High-order harmonic generation in polyatomic molecules generally involves multiple channels of ionization. Their relative contribution can be strongly influenced by the presence of resonances, whose assignment remains a major challenge for high-harmonic spectroscopy. Here we present a multi-modal approach for the investigation of unaligned polyatomic molecules, using SF6 as an example.

268 nm photodissociation of ClN3: a femtosecond velocity-map imaging study.

We report the first time-resolved study of the photochemistry of chlorine azide (ClN3) by femtosecond velocity-map imaging (fs-VMI). The dissociation dynamics are initiated at 4.6 eV and the photofragments are detected by multiphoton ionization using an intense laser field centered at 803 nm.

Communication: existence of the doubly excited state that mediates the photoionization of azulene.

We use the high-level electronic structure computations based on the equation-of-motion coupled-cluster (EOMCC) theory to show that the previously postulated [V. Blanchet et al., J.

Comparing femtosecond multiphoton dissociative ionization of tetrathiafulvene with imaging photoelectron photoion coincidence spectroscopy.

In this paper we describe femtosecond photoionization and the imaging photoelectron photoion coincidence spectroscopy of tetrathiafulvene, TTF. Femtosecond photoionization of TTF results in the absorption of up to twelve 808 nm photons leading to ion internal energies up to 12.1 eV as deduced from the photoelectron spectrum.