Quadricyclane Radical Cation Q+: Formation and Isomerization in Liquid Methylcyclohexane
Author:
Affiliation:
1. Laboratory for Physical Chemistry, ETH Zürich, Switzerland
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp993707k
Reference16 articles.
1. The t-0.6 Kinetic Law for Geminate Ion Kinetics and Its Applications To Non-Polar Solvents
2. The Radical Cation of Methylcyclohexane
3. A Precursor to the Solvent Radical Cation MCH+: Pulse Radiolysis of Liquid Methylcyclohexane (MCH) at 143 K
4. Chloroform Anion Fragmentation in Liquid Methylcyclohexane: t-0.6 Simulation of the Geminate Ion Kinetics
5. Quadir, M. A. Thesis, ETH Zürich, No. 11075, 1995.
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1. Isomerization pathways from the norbornadiene to the cycloheptatriene radical cation by opening a bridgehead-methylene bond: a theoretical investigation;Organic & Biomolecular Chemistry;2006
2. Quadricyclane Radical Cation Rearrangements: A Computational Study of the Transformations to 1,3,5-Cycloheptatriene and Norbornadiene;Chemistry - A European Journal;2004-02-06
3. Geminate Ion Kinetics for Hexa-, Penta- and Tetrachloroethane in Liquid Methylcyclohexane (MCH): Effect of the Anion Lifetimes;The Journal of Physical Chemistry A;2003-12-01
4. Anion of Tetrachloroethane (Tetra): Fragmentation and Geminate Ion Kinetics in Liquid Methylcyclohexane (MCH);The Journal of Physical Chemistry A;2003-12-01
5. Selective Alkane Transformations via Radicals and Radical Cations: Insights into the Activation Step from Experiment and Theory;Chemical Reviews;2002-04-17
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