## Abstract Various Cβcentered radicals can efficiently be generated through thermal Cο£ΏOβbond homolysis of alkoxyamines. This method is used to perform environmentally benign radical cyclization and intermolecular addition reactions. These alkoxyamine isomerizations and intermolecular carboaminoxyl
Simulation of free radical addition reactions modified by the presence of cobalt macrocycles
β Scribed by Thomas P. Davis; Dax Kukulj; Ian A. Maxwell
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 492 KB
- Volume
- 4
- Category
- Article
- ISSN
- 1022-1344
No coin nor oath required. For personal study only.
β¦ Synopsis
Free radical addition reactions in the presence of cobaloximes and related compounds have been modelled. Several mechanisms are presented and similarities with the "persistent radical effect" noted by Daikh and Finke are discussed. Cobaloximes and salophena) derivatives are widely used in organic synthesis to build carbon-carbon bonds, whereas in polymer synthesis they are used as catalytic chain transfer agents in the production of oligomers. This work shows that these reactions are closely related and also demonstrates the influence that an external radical source has on the overall reaction kinetics.
π SIMILAR VOLUMES
## Abstract The relative importance of bond strength, steric effects, and polarity in determining the rate and orientation of free radical subsitution and free radical addition reaction is considered. The factors which control substitution reaction (radical transfer reaction) are gathered together
## Abstract A cobalt(II) complex is paramagnetic and can be coordinated with sulfur functions; the coordination complex delocalizes an unpaired electron from cobalt(II) to the sulfur functions such as thioester and vinyl sulfide. Thus, the generation of partial unpaired electron density on the sulf