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19.11 : Mass Spectrometry of Amines

In mass spectroscopy, amines undergo fragmentation to give parent ions with odd molecule weights. This observed mass spectrum follows the nitrogen rule: a molecule with an odd number of nitrogen atoms produces a parent ion with an odd molecular weight. The remaining fragments have an even mass.

Amines undergo fragmentation through α cleavage, producing nitrogen-containing cations—iminium ions—and alkyl radicals. Mass spectra of aromatic and cyclic aliphatic amines exhibit strong molecular ion peaks, but acyclic aliphatic amines show weaker molecular ion peaks.

Tags
Mass SpectrometryAminesFragmentationParent IonsOdd Molecular WeightNitrogen RuleNitrogen containing CationsIminium IonsAlkyl RadicalsMolecular Ion PeaksAromatic AminesCyclic Aliphatic AminesAcyclic Aliphatic Amines

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19.11 : Mass Spectrometry of Amines

Amines

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19.1 : Amines: Introduction

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19.2 : Nomenclature of Primary Amines

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19.3 : Nomenclature of Secondary and Tertiary Amines

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19.4 : Nomenclature of Aryl and Heterocyclic Amines

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19.5 : Structure of Amines

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19.6 : Physical Properties of Amines

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19.7 : Basicity of Aliphatic Amines

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19.8 : Basicity of Aromatic Amines

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19.9 : Basicity of Heterocyclic Aromatic Amines

Amines

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19.10 : NMR Spectroscopy Of Amines

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19.12 : Preparation of Amines: Alkylation of Ammonia and Amines

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19.13 : Preparation of 1° Amines: Azide Synthesis

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19.14 : Preparation of 1° Amines: Gabriel Synthesis

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19.15 : Preparation of Amines: Reduction of Oximes and Nitro Compounds

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