Photochemically Induced 1,3-Butadiene Ring-Closure from the Topological Analysis of the Electron Localization Function Viewpoint

Chamorro, Eduardo

Abstract

The electronic rearrangement featuring the photochemically-induced 1,3-cis-butadiene is discussed within a bonding evolution theory (BET) perspective based on the topological analysis of the electron localization function and Thom's catastrophe theory. The process involves the vertical singlet-singlet excitation S0→S2, and the subsequent deactivation implying the S2/S1 and S1/S0 conical intersection regions. BET results reveal that the new CC bond is finally formed on the S0 surface, as also recently found in the photochemical addition of two ethylenes [Phys. Chem. Chem. Phys. 23, 20598, (2021)].

Más información

Título según WOS: Photochemically Induced 1,3-Butadiene Ring-Closure from the Topological Analysis of the Electron Localization Function Viewpoint
Título según SCOPUS: Photochemically Induced 1,3-Butadiene Ring-Closure from the Topological Analysis of the Electron Localization Function Viewpoint
Título de la Revista: ChemPhysChem
Volumen: 23
Número: 16
Editorial: John Wiley and Sons Inc.
Fecha de publicación: 2022
Idioma: English
DOI:

10.1002/cphc.202200217

Notas: ISI, SCOPUS