Hydride affinities of halogen substituted carbocations: the C2H4X+ (X = F, Cl or Br) cations
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry
Reference16 articles.
1. The Halogenation of Ethylenes
2. Reexamination of the C2H4F+ potential surface. the status of the classical 2-fluoroethyl cation: a local minimum or transition structure?
3. Relative stabilities of isomeric chlorine-substituted carbocations: the C2H4Cl+ cation
4. Structure and energetics of C2H4Br+: ethylenebromonium ion vs. bromoethyl cations
5. Isolation and the IR spectra of chloro- and bromo-ethyl cations in cryogenic SbF5matrices
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1. Theoretical Evidence for the Relevance of n(F) → σ*(C–X) (X = H, C, O, S) Stereoelectronic Interactions;The Journal of Organic Chemistry;2016-01-25
2. Transfer of F+ versus fluoronium metathesis;International Journal of Mass Spectrometry;2007-11
3. Ab initio and density functional study of substituent effects in halogenated cations of alkenes;Tetrahedron;2005-04
4. Structure and stability of halonium cations of cycloalkenes. A theoretical study;Tetrahedron;2003-06
5. Computational Studies of Halonium Ions of Cyclohexene and Cyclopentene;The Journal of Organic Chemistry;1998-11-12
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