The Photoelectron Spectra of Benzenoid Hydrocarbons C18H12
β Scribed by Dipl.-Chem. Franz Brogli; Prof. Dr. Edgar Heilbronner
- Publisher
- John Wiley and Sons
- Year
- 1972
- Tongue
- English
- Weight
- 219 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
In 1973, Hall noticed that the total -electron energy E of isomeric Ε½ . benzenoid hydrocarbons is a linear function of the number of Kekule structures K . Εince then, this remarkable rule has been confirmed on a plethora of examples. Twenty Ε½ . years later, it was discovered that for large benzenoid
Dimethoxysulfane / Dimethoxydisulfane / Photoelectron spectra / Calculations, MO / Ligand properties The He(1) photoelectron spectra of dimethoxysulfane (1) and dimethoxydisulfane (2) have been recorded. The lowest energy ionizations in the PE spectrum of 1 can be explained by assuming C , symmetry.
The n-ionization energies['] of alkyl-substituted triketones, as determined by photoelectron spectroscopy, can also be discussed on the basis of the calculated geometry of dimethyltriketone.
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