Quantitative relationships between fragment ions and their relative intensities in electron impact mass spectrometry: VI-Hydroxy-substituted tert-alkylamines
The influence of functional group interaction on the intensity ratios (Q) of product ions from α‐fission of ethyl‐tert‐alkylamines C2H5(C3H7)(HO(CH2)n)C NHC2H5, in which one side chain of the tert‐alkyl moiety is replaced by a hydroxyalkyl group of varying chain length, was investigated. It was fou...
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Veröffentlicht in: | Organic Mass Spectrometry 1982-04, Vol.17 (4), p.192-196 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The influence of functional group interaction on the intensity ratios (Q) of product ions from α‐fission of ethyl‐tert‐alkylamines C2H5(C3H7)(HO(CH2)n)C NHC2H5, in which one side chain of the tert‐alkyl moiety is replaced by a hydroxyalkyl group of varying chain length, was investigated. It was found that only through‐bond interaction between the functional groups has a major influence on these ratios. By substitution of a hydrogen by a halogen atom in one side chain it was shown that the so‐called ‘ion mass effect’ is a degrees of freedom effect. |
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ISSN: | 0030-493X 1096-9888 |
DOI: | 10.1002/oms.1210170408 |