Excited-state chemistry of the nitromethane anion mediated by the dipole-bound states revealed by photofragment action spectroscopy.

Abstract

We report the first experimental observation of the excited dipole-bound state (DBS) of the cryogenically cooled nitromethane anion (CH3NO2-), where the excess electron is loosely attached to the singlet or triplet neutral-core. Photofragment and photodetachment action spectra have been employed for the dynamic exploration of Feshbach resonances located even far above the electron detachment threshold, giving excitation profiles from the ground anionic state (D0) to the DBSs which match quite well with the spectral structures of the photoelectron spectra. This indicates that the electron transfer from the nonvalence orbital (of DBS) to the valence orbital (of anion) is mainly responsible for the anionic fragmentation channels, giving strong evidence for that the DBS plays a dynamic doorway-role in the anionic fragmentation reactions. Photofragment action spectra have also been obtained for the anionic clusters of (CH3NO2)2-, (CH3NO2)3-, or (CH3NO2·H2O)-, giving the relative yields of various fragments as a function of the excitation energy for each cluster. The absorption profiles of the anionic clusters exhibit substantial blue-shifts compared to the bare nitromethane anion as their ground states are much stabilized by solvation. The anionic fragmentation pattern varies among different clusters, giving essential clues for the thorough understanding of the whole anionic dynamics such as the dynamic role of the short-lived nonvalence-bound states of the clusters.