PNNL

Abstract

Negative Ion Photoelectron (NIPE) spectra of the radical anion of cyclopropane-1,2,3-trione, (CO)3•-, have been obtained at 20 K, using both 355 and 266 nm lasers for electron photodetachment. The spectra show broadened bands, due to the short lifetimes of both the singlet and triplet states of (CO)3. The smaller intensity of the band with the lower electron binding energy suggests that the singlet is the ground state of (CO)3. From the NIPE spectra, the electron affinity (EA) and the singlet-triplet energy gap of (CO)3 are estimated to be, respectively, EA = 3.1 ± 0.1 eV and ?EST = -14 ± 3 kcal/mol. High-level, (U)CCSD(T)/aug-cc-pVQZ//(U)CCSD(T)/aug-cc-pVTZ, calcu-lations give EA = 3.04 eV for the 1A1´ ground state of (CO)3 and ?EST = -13.8 kcal/mol for the energy gap between the 1A1´ and 3A2 states, in excellent agreement with values from the NIPE spectra. In addition, simulations of the vibrational structures for formation of these states of (CO)3 from the 2A2? state of (CO)3•- provide a good fit to the shapes of broad bands in the 266 nm NIPE spectrum. The NIPE spectrum of (CO)3•- and the analysis of the spectrum by high-quality electronic structure calculations demonstrate that NIPES can not only access and provide information about transition structures, but NIPES can also access and provide information about hilltops on potential energy surfaces.