Canadian Journal of Chemistry · 1972 · 207 citations · 2 references
Natural SciencesChemistryAnalytical ChemistryMass Spectrometric AnalysisPhysical ChemistryChemical PotentialMass SpectrometryRadical ReactionsStructural ElucidationFragmentation PathwaysIonizationMass Spectral Fragmentation
Using an energy-resolved electron beam, appearance potentials for[Formula: see text],[Formula: see text], and [Formula: see text] fragment ions from hydrocarbons of formula C 3 H 4 , C 3 H 6 , C 4 H 6 , C 4 H 8 , and C 5 H 10 have been measured. In each case the fragment appears to have a common structure, corresponding to [Formula: see text], [Formula: see text], and [Formula: see text]. Ionization potentials have been measured for propargyl radical (8.68 V), methallyl radical (7.54 V), and 2-methylallyl radical (7.89 V). Corresponding ionic heats of formation are propargyl 281 ± 3 kcal/mol, methallyl 204 ± 3 kcal/mol, and 2-methylallyl 211 ± 5 kcal/mol. The [Formula: see text] fragment ion is 25 kcal/mol more stable than propargyl ion, and is almost certainly cyclopropenyl ion. Ionization potentials for propyne, allene, cyclopropene, 1- and 2-butyne, and fifteen isomers of formula C n H 2n have also been measured by monoenergetic electron impact.
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Thermochemistry of organic and organometallic compounds
J. B. Pedley · Journal of Organometallic Chemistry · 1970 · 1.2K citations