Mass spectra of some azoles
β Scribed by J. L. Cotter
- Publisher
- John Wiley and Sons
- Year
- 1972
- Tongue
- English
- Weight
- 221 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1076-5174
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β¦ Synopsis
The principal electron-impact fragmentation patterns of 3,4,5-triphenyl-l,2,4-triazole, 2,5-diphenyl-l,3,4-thiadiazole, their perfluorinated analogues and 2,5-di(pentafluorophenyl)-1,3,4oxadiazole have been established from metastable ion evidence and precise mass measurements. Although ions produced by expulsion of nitrogen from the molecular-ions of these compounds are of low abundance, the simultaneous expulsion of nitrogen and a C,Xs radical (X = H or F) gives rise to abundant ions.
* Although a metastable peak corresponding to the transition [MI+. + 180+ + 117 was not observed in the spectrum of I, the simultaneous elimination of nitrogen and a C,F, radical from the molecular-ion of I1 is substantiated by an appropriate metastable peak.
π SIMILAR VOLUMES
## Abstract The mass spectra of a number Oβalkylthionocarbamates with two, one or no alkyl substituents on the nitrogen atom are presented and discussed. The main primary fragmentation pathways are McLafferty rearrangements, including the double soβcalled protonated McLafferty rearrangement. Genera