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...

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Autores principales: Nudelman, N.S., Waisbaum, R.G.
Formato: JOUR
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_0030493X_v13_n2_p61_Nudelman
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spelling todo:paper_0030493X_v13_n2_p61_Nudelman2023-10-03T14:40:38Z Mass spectra of o‐aminobenzophenones Nudelman, N.S. Waisbaum, R.G. 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 [MH]+ 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 JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_0030493X_v13_n2_p61_Nudelman
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
description 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 [MH]+ 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
format JOUR
author Nudelman, N.S.
Waisbaum, R.G.
spellingShingle Nudelman, N.S.
Waisbaum, R.G.
Mass spectra of o‐aminobenzophenones
author_facet Nudelman, N.S.
Waisbaum, R.G.
author_sort Nudelman, N.S.
title Mass spectra of o‐aminobenzophenones
title_short Mass spectra of o‐aminobenzophenones
title_full Mass spectra of o‐aminobenzophenones
title_fullStr Mass spectra of o‐aminobenzophenones
title_full_unstemmed Mass spectra of o‐aminobenzophenones
title_sort mass spectra of o‐aminobenzophenones
url http://hdl.handle.net/20.500.12110/paper_0030493X_v13_n2_p61_Nudelman
work_keys_str_mv AT nudelmanns massspectraofoaminobenzophenones
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