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Ammonia chemical ionization mass spectrometry of alcohols: Structural,stereochemical, molecular-size and temperature effects
Authors:Fazil O Gülaar  Franois Mermound  F Johann Winkler  Armand Vuchs
Institution:Fazil O. Gülaçar,François Mermound,F. Johann Winkler,Armand Vuchs
Abstract:Ammonia chemical ionization (CI) mass spectra of various open-chain, cyclic and unsaturated C5- to C10-alcohols were obtained at source temperatures ranging from 60° to 250°C. The reactivity of the ammonia adduct ion MNHurn:x-wiley:0018019X:media:HLCA19840670219:tex2gif-stack-1 and its fragmentation channels are characteristic for substrate structure. Although strongly temperature-dependent, the spectra give nevertheless information on the OH-group environment as well as on the C-skeleton at any source temperature. Primary, secondary and tertiary alcohols as well as allylic and simple olefinic alcohols can be distinguished by their spectra, which show ammonium adduct ions MNH4]+, adduct dehydrogenation ions MNH4-H2], ammonium substitution ions MNH4-H2O]+ and M-OH]+-ions as the main characteristic peaks. Moreover, konfigurational assignments of stereoisomeric alcohols are possible for larger substrate-size and source-temperature ranges than with isobutane CI mass spectrometry. Homologous M NHurn:x-wiley:0018019X:media:HLCA19840670219:tex2gif-stack-2-ions show molecular-size control of fragmentation and linear MNHurn:x-wiley:0018019X:media:HLCA19840670219:tex2gif-stack-3-ions are less stable than branched isomers due to incomplete energy randomization.
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