Organic Mass Spectrometry · 1986 · 33 citations · 9 references
Natural SciencesChemistryAnalytical ChemistryMass Spectrometric AnalysisSpectroscopyCarboxylic AcidsFatty Acid ChemistryInstrumental AnalysisIonization TechniquesMass SpectrometryStructural ElucidationCarboxylate AnionsFatty Acid Methyl EstersFragmentation PathwaysIonizationMass Spectral FragmentationMass Spectrometric IdentificationMass Spectrometric Structural ElucidationNegative Ionization
Abstract Saturated and mono‐unsaturated fatty acid methyl esters as well as corresponding underivatized acids gave abundant carboxylate anions [RCOO] − under negative ion chemical ionization (OH − and NH 2 − ) and electron attachment conditions. B/E or mass‐analysed ion kinetic energy spectra of fragments arising from high energy collision activated dissociation (CAD) of these [RCOO] − species contained decisive information on the original structure of the neutrals. From an analytical point of view, the method can utilize the gas chromatographic mass spectrometric combination and, in the B/E mode, can be used in practice on any double‐focusing mass spectrometer.
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