Ab-initio studies of radical cations derived from hexa-1,5-diene systems: semibullvalene
β Scribed by Roth, Heinz D.; Lakkaraju, Prasad S.
- Book ID
- 124102414
- Publisher
- American Chemical Society
- Year
- 1993
- Tongue
- English
- Weight
- 589 KB
- Volume
- 97
- Category
- Article
- ISSN
- 0022-3654
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Molecular orbital calculations were carried out to interpret the reaction behavior of the formation reaction and structural feature of double Diels-Alder (DDA) adduct derived from three-step sequential pericyclic reactions of 2-pyrone with cycloocta-1,5-diene. The experimental results are correctly
Abstraet--l,2,4,5-Tetramesitoylbenzene was synthesized and reduced with alkali metals as well as electrolytically. EPR spectra of the resulting radical-ion pairs are reported and discussed. The electron-spin densities obtained from splitting constants are compared to the results of MO calculations.