Photochemically Induced 1,3-Butadiene Ring-Closure from the Topological Analysis of the Electron Localization Function Viewpoint
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 S-0 -> S-2, and the subsequent deactivation implying the S-2/S-1 and S-1/S-0 conical intersection regions. BET results reveal that the new CC bond is finally formed on the S-0 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 de la Revista: | CHEMPHYSCHEM |
Volumen: | 23 |
Número: | 16 |
Editorial: | WILEY-V C H VERLAG GMBH |
Fecha de publicación: | 2022 |
DOI: |
10.1002/cphc.202200217 |
Notas: | ISI |