Mass spectra of o‐aminobenzophenones
The electron impact induced fragmentation of chlorine substituted o‐aminobenzophenones has been examined. All the compounds show ions formed by α‐cleavage on either side of the carbonyl group. The relative intensity of the resulting ions is predictable from the quasi‐equilibrium theory. The most imp...
Guardado en:
| Publicado: |
1978
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| Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0030493X_v13_n2_p61_Nudelman http://hdl.handle.net/20.500.12110/paper_0030493X_v13_n2_p61_Nudelman |
| Aporte de: |
| Sumario: | The electron impact induced fragmentation of chlorine substituted o‐aminobenzophenones has been examined. All the compounds show ions formed by α‐cleavage on either side of the carbonyl group. The relative intensity of the resulting ions is predictable from the quasi‐equilibrium theory. The most important features of the mass spectra of these compounds are, however, intense [MH]+ ions for the primary amines and [M – OH]+ ions for the N‐methylated compounds. These and other less intense peaks as well as some metastable ions allows structural elucidation. Copyright © 1978 Heyden & Son Ltd |
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