The effect of configuration of gas phase protonated ethenedicarboxylates on their low energy collision induced dissociation behaviour

作者: A. Weisz , A. Mandelbaum , J. Shabanowitz , D. F. Hunt

DOI: 10.1002/OMS.1210190508

关键词: ProtonationCis–trans isomerismSpectral lineChemistryCollision-induced dissociationDouble bondStereospecificityMass spectrometryMedicinal chemistryStereochemistryIonInstrumentation (computer programming)Molecular medicineBiochemistry

摘要: Low energy collision induced dissociation (CID) spectra were measured by a triple stage quadrupole mass spectrometer for the [MH]+ ions of diethyl and dimethyl esters maleic, fumaric, citraconic mesaconic acids. A very high degree stereospecificity was observed geometrically isomeric esters. The cis give rise to abundant [MHEtOH]+ [MHEtOHC2H4]+ ions, while trans isomers exhibit [MHC2H4]+ [MH2 C2H4]+ ions. highly stereospecific processes indicate that double bond configuration is retained in protonated species under conditions experiment.

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