Ion-Molecule Reactions of CH5+, C2H5+, and C3H5+ with Halogenated Benzenes in an Ion-Trap Type of a Mass Spectrometer
Author:
Publisher
The Mass Spectrometry Society of Japan
Link
http://www.jstage.jst.go.jp/article/massspec/59/4/59_11-21/_pdf
Reference33 articles.
1. 1) “有機化学講座1, 有機反応,脂肪族化合物”,丸善(1984).
2. 2) 長倉三郎,“有機電子理論”,培風館(1966).
3. Super acids. III. Protonation of alkanes and intermediacy of alkanonium ions, pentacoordinated carbon cations of CH5+ type. Hydrogen exchange, protolytic cleavage, hydrogen abstraction; polycondensation of methane, ethane, 2,2-dimethylpropane and 2,2,3,3-tetramethylbutane in FSO3H-SbF5
4. Electrophilic reactions at single bonds. III. H-D exchange and protolysis (deuterolysis) of alkanes with superacids. The mechanism of acid-catalyzed hydrocarbon transformation reactions involving the .sigma. electron pair donor ability of single bonds via three-center bond formation
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