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- W2019966505 abstract "The field ionization mass spectra of monosubstituted cyclopentenes and cyclohexenes with C1-C7 n-alkyl and C4-C5 isoalkyl substituents in positions 1 and 3 have been investigated and compared with the previously reported electron impact mass spectra of these compounds. The cleavage of the CC bond β to the double bond in the non-isomerized molecular ion was found to be a typical degradation reaction of the higher homologues in the strong electric field. So, by means of the field ionization mass spectra, the >C1 alkyl substituent can be readily located in the parent molecule. The electron impact mass spectra exhibit a less specific fragment ion distribution for positional isomers due to the extensive molecular ion isomerization prior to decomposition, but provide useful information on the ring size. For structure determination it is appropriate to use both ionization techniques." @default.
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- W2019966505 date "1984-04-01" @default.
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- W2019966505 title "Field ionization and electron impact mass spectra of cycloolefins" @default.
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- W2019966505 doi "https://doi.org/10.1002/oms.1210190409" @default.
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