Dichlorocarbene Addition To Cyclopropenes: A Computational Study
Document Type
Article
Publication Date
3-4-2005
Published In
Journal Of Organic Chemistry
Abstract
Reaction paths for addition of dichlorocarbene to 1,2-disubstituted cyclopropenes were calculated using hybrid density functional theory (B3LYP/6-31G") in the gas phase and in the presence of a continuum solvation model corresponding to acetonitrile. In both the gas phase and acetonitrile, :CCl2-cyclopropene addition follows an asymmetric, non-least-motion approach. Barriers to addition range from 0 to 2 kcal/mol. The reactions proceed in concerted fashion in both the gas phase and solution to yield 1,3-dienes or bicyclobutanes. The reaction pathway on this complex potential energy surface of this reaction appears to bifurcate, and the product distribution is believed to be controlled by reaction dynamics. At the present level of theory, there appears to be no minimum on the potential energy surface corresponding to a dipolar intermediate.
Recommended Citation
D. C. Merrer and Paul R. Rablen.
(2005).
"Dichlorocarbene Addition To Cyclopropenes: A Computational Study".
Journal Of Organic Chemistry.
Volume 70,
Issue 5.
1630-1635.
DOI: 10.1021/jo048161z
https://works.swarthmore.edu/fac-chemistry/82