## Abstract The electronic structure of quadricyclane and 3‐methylidenequadricyclane obtained by photoelectron spectroscopy, is used as a basis for the discussion of cycloadditions to these systems. The electronic structure of 3‐heteroquadricyclanes, arrived at by theoretical calculations, agrees w
Quadricyclanes. Part I: Photoelectron spectra and electronic structure
✍ Scribed by Hans-Dieter Martin; Constanze Heller; Edwin Haselbach; Zuzana Lanyjova
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- German
- Weight
- 345 KB
- Volume
- 57
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The photoelectron spectra of quadricyclane (3) and 3‐methylidene quadricyclane (4) have been measured. The results served as a basis for the elucidation of the electronic structure of these compounds, which agreed with theoretical calculations. It is found that the symmetry of the HOMO of 3 is different when compared to that of its valence isomer norbornadiene (1). The results also indicate that the structure of the highest occupied orbitals cannot be derived by only considering the Walsh‐orbitals of the two three‐membered rings. In addition one of the Walsh‐components of the four‐memebered ring has to be taken into account.
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