Why Does Perfluorination Render Bicyclo[2.2.0]hex-1(4)-ene Stable toward Dimerization? Calculations Provide the Answers
Author:
Affiliation:
1. Contribution from the Department of Chemistry, University of North Texas, P.O. Box 305070, Denton, Texas 76203-5070
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja063848h
Reference35 articles.
1. Bicyclo[2.2.0]hex-1(4)-ene
2. Enthalpies of formation of fused cyclobutane derivatives
3. Group equivalents for convertingab initio energies to enthalpies of formation
4. Pyramidalized alkenes
5. Perspective on Fluorocarbon Chemistry
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