Calculation of the electronic and photoelectronic spectra of nitroso compounds: A reinvestigation by use of configuration interaction methods
Résumé
The electronic properties of three selected nitroso compounds: nitrosyl chloride (NOC1), nitrosomethane (CH3NO) and trichloronitrosomethane (CC13NO) have been compared, and their UV and photoelectron spectra calculated within an extensive configuration interaction treatment. Triple ζ Dunning basis set for NOC1 and pseudo potentials basis sets for CX3NO, complemented with Rydberg orbitals for the calculation of the UV spectrum have been used. The visible band of the UV spectra of the three compounds is attributed to a 1A' state: it is a triplet state for NOC1 due to spin-orbit splitting, and a singlet state for the two other compounds. In the case of NOC1 and CH3NO, some Rydberg orbitals are involved in the short wave-lengths transitions. However, the corresponding band is poorly resolved in the case of NOC1 and not recorded in this region for CH3NO. For CCl3NO, the UV spectrum is much simpler. For the photoelectronic spectra of the three compounds, the presence of a low-lying unoccupied orbital located on π((z)/*)((NO)) induces some defect to Koopmans' theorem and to the one-particle model of ionization. These results imply that the experimental spectrum of NOC1 has to be reassigned in this scheme.