Proximity effects in the electron ionisation mass spectra of substituted cinnamamides.

ABSTRACT: The electron ionisation mass spectra of an extensive set of 53 ionised monosubstituted and disubstituted cinnamamides [XC₆H₄CH=CHCONH₂, X = H, F, Cl, Br, I, CH₃, CH₃O, CF₃, NO₂, CH₃CH₂, (CH₃)₂CH and (CH₃)₃C; and XYC₆H₃CH=CHCONH₂, X = Y = Cl; and X, Y = F, Cl or Br] are reported and discussed. Particular attention is paid to the significance of loss of the substituent, X, from the 2-position, via a rearrangement that is sometimes known as a proximity effect, which has been reported for a range of radical-cations, but is shown in this work to be especially important for ionised cinnamamides. When X is in the 2-position

SUBMITTER: Michalik AR 

PROVIDER: S-EPMC10068410 | biostudies-literature | 2023 Apr

REPOSITORIES: biostudies-literature