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Stereochemical applications of mass spectrometry 4. Energy‐resolved study of the fragmentation of esters of maleic and fumaric acids
Author(s) -
Harrison Alex G.,
Nacson Sabatino,
Mandelbaum Asher
Publication year - 1987
Publication title -
organic mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.475
H-Index - 121
eISSN - 1096-9888
pISSN - 0030-493X
DOI - 10.1002/oms.1210220510
Subject(s) - chemistry , fragmentation (computing) , ion , maleic anhydride , metastability , mass spectrum , polyatomic ion , fumaric acid , organic chemistry , copolymer , polymer , computer science , operating system
The fragmentation of the dimethyl and diethyl esters of maleic and fumaric acids have been studied as a function of the internal energy of the molecular ions using charge exchange techniques and metastable ion studies in combination with isotopic labelling. The dimethyl ester molecular ions show distinctive behaviours at both low and high internal energies, indicating that interconversion of the molecular ions does not occur. The fumarate molecular ion fragments by elimination of CH 2 O and (CO 2 + CH 3 ) in the metastable ion time‐frame, while the maleate ester fragments primarily by loss of CH 3 O. At higher internal energies both molecular ions fragment primarily by loss of CH 3 O but the fragment ion from the maleate ester shows a greater stability, presumably because it assumes the cyclic cationated maleic anhydride structure. The diethyl maleate and diethyl fumarate molecular ions show identical metastable ion characteristics; in addition the [COS] + · charge exchange mass spectra are very similar. These results indicate that low‐energy molecular ions interconvert. At higher internal energies interconversion does not occur, and, although both moiecular ions fragment by loss of C 2 H 5 O, the resultsint fragment ions show different stabilities and fragmentation reactions.