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Electron impact mass spectra of some tertiary aliphatic nitro compounds. Nitrocarbonyl compounds and some analogues

✍ Scribed by Leszek Konopski; Karol Grela


Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
462 KB
Volume
27
Category
Article
ISSN
1076-5174

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✦ Synopsis


Tbe mass spectra of some tertiary aliphatic nitroaldehydes, nitroketows, nitroesters, nitronitriles a d related nitro-carbony1 compounds are discussed and compared with those of some analogous nitro compounds lacking tbe car-bony1 function. The M" -NO,' and in several cases M" -HNO, fragmentations seem to be the most characteristic features of all tertiary aliphatic nitro compounds. In the presence of tbe primary nitro group, the loss of HNO, is always observed. Table 2. Mass spectras of aliphatic nitro compounds without a carbonyl substituent, (CH,),C(NO,)R (16-21) Compound No. 16 Twelve most intense peaks, m/z (relative intensity. "h)


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Electron impact mass spectra of some sub
✍ Sureerat Singhawangcha; Colin F. Pooie; Albert Zlatkis πŸ“‚ Article πŸ“… 1980 πŸ› John Wiley and Sons 🌐 English βš– 286 KB

## Abstract The electron impact mass spectra of the 3,5‐bis(trifluoromethyl)benzeneboronate, 2,4‐dichlorobenzene‐boronate and 4‐bromobenzeneboronate derivatives of some bifunctional diols and aminoalcohols are characterized by prominent molecular ions with diagnostically useful modes of fragmentati