The photoionization of CF3I molecules in the photon energy range between 10 eV and 40 eV is investigated using angle-resolved photoelectron spectroscopy in the molecular frame. Using a femtosecond laser pulse, the molecules are impulsively aligned prior to their ionization by a series of extreme ultra-violet photon energies obtained by high-harmonic generation. The manifestation of molecular alignment in the photoelectron angular distributions (PADs) is well reproduced by non-relativistic quantum-mechanical photoionization calculations carried out with the ePolyScat software package, taking into account all open ionization channels. Our analysis points to two prominent shape resonances that dominate the photoelectron scattering dynamics and that therefore largely explain the observed changes in the PADs as a function of molecular alignment.
