The 70 eV electron impact mass spectra of 33 differently substituted oxazolidines were studied to determine the effect of substituents and the existence of the ring-chain tautomeric equilibrium on the decomposition of the molecular ions. Most of the fragmentations can be rationalized to start as the
Mass spectrometric behaviour of cyclopentane-and cyclohexane-condensed pyrimidinediones under electron impact
✍ Scribed by Marja Himottu; Kalevi Pihlaja; Gábor Bernáth; Géza Stájer; Pirjo Vainiotalo
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 534 KB
- Volume
- 25
- Category
- Article
- ISSN
- 1076-5174
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✦ Synopsis
Mass spectral fragmentations of four cyclopentane-condensed cis-pyrimidinediones and of six cyclohexanecondensed cis-or trans-pyrimidinediones were examined using metastable ion analyses and exact mass measurements. The fragmentation patterns of all of these compounds were clearly different and also cis-and trans-fused isomers were easy to distinguish from each other by their mass spectra. In spite of the differences in their mass spectral fragmentations, all compounds formed phenylisocyanates (m/z 119 and 153) and anilines (m/z 93 and m/z 127), the structures of which were verified by collision-induced dissociation experiments.
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