| Literature DB >> 29694047 |
Joshua P Rogers1, Cate S Anstöter1, Jan R R Verlet1.
Abstract
Frequency-resolved photoelectron spectra are presented for (C6F6) n- with n = 1-5 that show that C6F6- is solvated by neutral C6F6 molecules. Direct photodetachment channels of C6F6- are observed for all n, leaving the neutral in the S0 ground state or triplet states, T1 and T2. For n ≥ 2, an additional indirect electron loss channel is observed when the triplet-state channels open. This indirect emission appears to arise from the electron capture of the outgoing photoelectron s-wave by a neutral solvent molecule through an anion nonvalence state. The same process is not observed for the S0 detachment channel because the outgoing electron wave is predominantly a p-wave. Our results show that anion nonvalence states can act as electron-accepting states in cluster environments and can be viewed as precursor states for diffuse states of liquid C6F6.Entities:
Year: 2018 PMID: 29694047 DOI: 10.1021/acs.jpclett.8b00739
Source DB: PubMed Journal: J Phys Chem Lett ISSN: 1948-7185 Impact factor: 6.475