Ab initio quantum-chemical study of the unimolecular pyrolysis mechanisms of fluoroformic and chloroformic acid
β Scribed by J.S. Francisco; W.A. Ghoul
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 687 KB
- Volume
- 157
- Category
- Article
- ISSN
- 0301-0104
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The Brandi reaction is the transformation of spiro[cyclopropane-1,5Π-isoxazolidines] into tetrahydropyridones under thermal conditions. According to calculations performed by the restricted and unrestricted density functional theory and post-Hartree-Fock single-and multireference methods of ab initi
A Theoretical Study on the Mechanism of the Superacid-Catalyzed Unimolecular Isomerization of n-Alkanes and n-Alkenes. Comparison Between ab initio and Density Functional Results -(in predicting transition state properties and activation energies of branching rearrangement of 2-pentyl cation, which