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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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 |
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paper:paper_0030493X_v13_n2_p61_Nudelman2023-06-08T14:56:27Z 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 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 1978 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 |
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 [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 |
title |
Mass spectra of o‐aminobenzophenones |
spellingShingle |
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 |
publishDate |
1978 |
url |
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 |
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1768543359627952128 |