Reactivity of Organic Ions by Chemical Ionization Mass Spectrometry. II. Chemical Ionization Mass Spectra of Alkylbenzenes with Methane by Using a Quadrupole Mass Spectrometer
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/51/7/51_7_2167/_pdf
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4. Solubility of Hydrogen Chloride at Low Temperatures. A Measure of the Basic Properties of Aromatic Nuclei; π- and σ-Complexes and Their Role in Aromatic Substitution1,2
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1. Loss of methane and ethene from long-lived gaseous xylenium ions (protonated xylene) after “composite” scrambling;International Journal of Mass Spectrometry;2002-09
2. Protonated 1,3,5-cycloheptatriene and 7-alkyl-1,3,5-cycloheptatrienes in the gas phase: ring contraction to the isomeric alkylbenzenium ions;Journal of Mass Spectrometry;1999-04
3. Intramolecular reactions. An explanation for [M−H]+ ions in the chemical ionization mass spectra of some ring C-substituted methyl dehydroabietate derivates;Rapid Communications in Mass Spectrometry;1997-10-15
4. The origin of M+˙ in the chemical ionization mass spectra of polymethylbenzenes;Organic Mass Spectrometry;1988-08
5. Characterization of C8H10 alkylbenzenes by negative ion mass spectrometry;Organic Mass Spectrometry;1988-02
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