Mass spectra of the fluorosulfates could not be obtained, since decomposition and polymerisation took place.
The Interaction of Walsh-Orbitols in Diademane and Related Hydrocarbons
✍ Scribed by Edgar Heilbronner; Rolf Gleiter; Toshihiko Hoshi; Armin de Meijere
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- German
- Weight
- 523 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
To obtain further information concerning the interaction between Walsh‐orbitols of ‘conjugated’ cyclopropane rings, the photoelectron spectra of the following compounds have been recorded: bicyclo[4.1.0]heptane 1, cis‐ and trans‐tricyclo[5.1.0^3, 5^]octane 2, 3, diademane 4, trans‐pentacyclo[3.3.2.0^2, 9^.0^4, 10^, 0^6, 8^]decan 5 and bicyclo[4.1.0]heptene‐2 6. The first bands in the PE.‐spectra of these compounds have been assigned on the basis of a ZDO HMO‐approximation. For 2 and 4 the value for resonance integral between linked 2p atomic orbitals of two adjacent eclipsed cyclopropane rings is found to be −1.73 eV.
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Composition and structure of (2) were proved by chemical analysis, mass spectrum, NMR data (31P[41, 'H, "Si) and by complete X-ray structure analysis. The 'H-NMR spectrum (10% solution in CH2C12; TMS int.[\*], 25°C) shows three groups of signals with equal intensity-{ 31P} : three singlets-which in
## Abstract Photoelectron spectra of __endo__‐ and __exo__‐cyclopropano‐norbornene ( = __endo__‐ and __exo__‐tricyclo[3.2.1.0^2.4^]octa‐6‐ene) show that a significant homoconjugation exists between the π‐orbital of the double bond and the symmetric __Walsh__‐__es__‐orbital of the cyclopropane ring