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Structure and fragmentation of dimethyl methylphosphonate and trimethyl phosphite
Author(s) -
Holtzclaw James R.,
Wyatt Jeffrey R.,
Campana Joseph E.
Publication year - 1985
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.1210200205
Subject(s) - dimethyl methylphosphonate , isomerization , chemistry , fragmentation (computing) , dissociation (chemistry) , ion , electron ionization , enol , molecule , collision induced dissociation , photochemistry , ionization , mass spectrometry , organic chemistry , tandem mass spectrometry , catalysis , chromatography , computer science , operating system
The structures and fragmentation pathways of two isomeric organophosphorus esters, dimethyl methylphosphonate (DMMP) and trimethyl phosphite (TMP) have been determined. The long‐lived, low‐energy molecular ions of DMMP were found to undergo a keto‐to‐enol isomerization prior to collision‐induced dissociation. This isomerization was established through the comparison of the collision spectra from DMMP, TMP, isotopically labeled DMMP and a model precursor ion. Electron ionization and charge exchange reactions were used to study the isomerization as a function of the internal energy of the molecular ion. The structure of the TMP molecular ion retained the structure of the neutral molecule. The daughter ion spectra of the isomeric fragment ions from DMMP and TMP were used to infer the fragment ion structures. Negative ions of DMMP and TMP were also studied, and their collision spectra were found to be indistinguishable.

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