Photoelectron spectroscopy and circular dichroism of a chiral metal\u2013organic complex

A comparison between theoretical and experimental results for the photoelectron intensity and circular dichroism is reported for the valence electron states of the metal complex D-Cobalt(III) tris-acetylacetonate. The measured intensities of the valence features and their dichroic behaviour are reproduced in the time dependent density functional theory (TDDFT) framework. The satisfactory agreement between theoretical and experimental results in the photon energy range 15\u201329 eV proves that the TDDFT procedure is suitable for describing electronic processes and circular dichroism