The chemical ionization mass spectra of eight monoterpene alkaloids from the gentianine group and their derivatives were investigated. Isobutane, methanol, ammonia, methylamine, ethylenediamine, diethylamine and triethylamine were used as reactant gases. The application of this technique for investi
Ionization energies of selenophen, tellurophen and some of their derivatives
β Scribed by G. Distefano; S. Pignataro; G. Innorta; F. Fringuelli; G. Marino; A. Taticchi
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- English
- Weight
- 392 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
The ionizaiion energies ofselenophcn.
tcllurophen and a number of derivatives have been determined by the clectron impact tcchniquc. Comp;jrison of the values obtained for tellurophen with those referring to the other 5-membered rings reveals twcj major diffcrcnccs: (1) the IP of the onsubstituted tcllurophcn is significantly Ioaer than thnt of its congencrs; (2) the sensitivity to substitucnt effects is much smaller. The peculiar behaviour of tellurophen with respect to rhc other congcncr systems can be esplaincd by admitting that B different molecular orbital is involved in the first ionization process of this ring. This is confirmed by photoelectron spectroscopy measurements.
π SIMILAR VOLUMES
Matsen equations are used in order to calculate, for the investigated compounds, related series of ionization potentials and electron affinities in gaseous phase, aqueous solution and in the photographic emulsion. More especially, peak and conventional polarographies are used to determine the oxida