Electronic structure and spectroscopy of oxyallyl: A theoretical study

Vadim Mozhayskiy, Daniel J. Goebbert, Luis Velarde, Andrei Sanov, Anna I. Krylov

Research output: Contribution to journalArticle

24 Scopus citations

Abstract

Electronic structure of the oxyallyl diradical and the anion is investigated using high-level ab initio methods. Converged theoretical estimates of the energy differences between low-lying electronic states of oxyallyl (OXA) as well as detachment energies of the anion are reported. Our best estimates of the adiabatic energy differences between the anion 2A2 and the neutral 3B2 and 3B1 states are 1.94 and 2.73 eV, respectively. The 1A1 state lies above 3B2 vertically, but geometric relaxation brings it below the triplet. The two-dimensional scan of the singlet 1A 1 potential energy surface (PES) reveals that there is no minimum corresponding to a singlet diradical structure. Thus, singlet OXA undergoes prompt barrierless ring closure. However, a flat shape of the PES results in the resonance trapping in the Franck-Condon region, giving rise to the experimentally observable features in the photoelectron spectrum. By performing reduced-dimensionality wave packet calculations, we estimated that the wave packet lingers in the Franck-Condon region for about 170 fs, which corresponds to the spectral line broadening of about 200 cm-1. We also present calculations of the photodetachment spectrum and compare it with experimental data. Our calculations lend strong support to the assignment of the photoelectron spectrum of the OXA anion reported in Ichino et al. (Angew. Chem., Int. Ed. Engl. 2009, 48, 8509).

Original languageEnglish (US)
Pages (from-to)6935-6943
Number of pages9
JournalJournal of Physical Chemistry A
Volume114
Issue number26
DOIs
StatePublished - Jul 8 2010

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry

Fingerprint Dive into the research topics of 'Electronic structure and spectroscopy of oxyallyl: A theoretical study'. Together they form a unique fingerprint.

  • Cite this