10min:

ELENA N. LARICHEVA AND MASSIMO OLIVUCCI, Department of Chemistry and Center for Photochemical Sciences, Bowling Green State University, Bowling Green, OH 43403, USA; JAKOB GRILJ AND ERIC VAUTHEY, Physical Chemistry Department, University of Geneva, 1211 Geneva, Switzerland.

\indent The photochemistry and photophysics of a stable N,N,N',N'- tetramethyl- p -phenylenediamine radical cation (commonly known as Wurster’s Blue) is the subject of current research interest as it represents an example of mixed valence (MV) compound. In this work we used ab initio CASSCF/CASPT2 quantum chemical calculations to map its first excited state (D₁) potential energy surface in the gas-phase.

\indent According to the spectral data by Grilj et al., the fluorescence of Wurster’s Blue radical cation could only be observed at low temperatures (below 115K). In order to explain this behavior, the conical intersection space (IS) between the first excited (D₁) and the ground state (D₀) potential energy surfaces was mapped and characterized. The intrinsic reaction coordinate (IRC) scan, following the relaxation of the Wurster’s blue molecule from the D₁/D₀ intersection space along the D₀ potential energy surface, led to the ground state equilibrium structure. The energy barrier between the excited state energy minimum and the lowest lying conical intersection structure (CI) was calculated to be 3.1 kcal/mol. As a result, we concluded that this barrier was responsible for the observed temperature dependence of the fluorescence that disappears at temperatures above 115K due to the opening of a radiationless deactivation channel.