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 S0âS2, 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 |