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- W2034341693 abstract "Collisional activation mass spectra confirm that tolyl ions can be produced from a variety of CH3C6H4Y compounds. High purity o-, m- and p-tolyl ions are prepared by chemical ionization of the corresponding fluorides (Y=F) as proposed by Harrison. In electron ionization of CH3C6H4Y formation of the more stable tropylium and benzyl ionic isomers usually accompanies that of the o-, m- and p-tolyl ions. Isomerization of low energy [CH3C6H4Y]+⋅ to [Y–methylenecyclohexadiene]+⋅ is proposed to account for most [benzyl]+ formation, while the tropylium ion appears to arise from the isomerization of tolyl ions formed with higher internal energies, [o-, m-, p-tolyl]+→ [benzyl]+→ [tropylium]+, consistent with Dewar's predictions from MINDO/3 calculations." @default.
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- W2034341693 date "1979-03-01" @default.
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- W2034341693 title "Formation and stability of gaseous tolyl ions" @default.
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- W2034341693 doi "https://doi.org/10.1002/oms.1210140402" @default.
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