Dissociative Photoionization of 1-Halogenated Silacyclohexanes: Silicon Traps the Halogen
Author:
Affiliation:
1. Laboratory for Femtochemistry and Synchrotron Radiation, Paul Scherrer Institute, 5232 Villigen, Switzerland
2. Science Institute, University of Iceland, Dunhaga 3, 107 Reykjavík, Iceland
Funder
Seventh Framework Programme
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.jpca.6b09195
Reference63 articles.
1. The anomeric effect in substituted cyclohexanes. I. The role of hyperconjugative interactions and steric effect in monosubstituted cyclohexanes
2. The anomeric effect in substituted cyclohexanes. II. The role of hyperconjugative interactions and steric effect in 1,4-disubstituted cyclohexanes
3. The Nonexistence of Repulsive 1,3-Diaxial Interactions in Monosubstituted Cyclohexanes
4. Conformations of Silicon-Containing Rings. 5., Conformational Properties of 1-Methyl-1-silacyclohexane: Gas Electron Diffraction, Low-Temperature NMR, and Quantum Chemical Calculations
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2. Dissociative Photoionization of Chloro-, Bromo-, and Iodocyclohexane: Thermochemistry and the Weak C–Br Bond in the Cation;The Journal of Physical Chemistry A;2021-01-11
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4. Conformers, electronic states, and diabolical conical intersections in the valence photoelectron spectroscopy of halocyclohexanes;The Journal of Chemical Physics;2020-08-07
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