THE MECHANISM of aromatic phenylation has been an object of considerable interest over the past 25 years. 2 Most authors presently seem to accept the view that the process involves two, separate stages. When benzoyl peroxide is the source Ph.
Solvent effects on free radical formation. Thermolysis of phenylazotriphenylmethane
β Scribed by Wesley G. Bentrude; Allen K. MacKnight
- Publisher
- Elsevier Science
- Year
- 1966
- Tongue
- French
- Weight
- 201 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
The role played by solvent in the reactions of organic molecules is not well understood. One is often tempted to try to interpret solvent effects on processes in which ions or molecules are formed solely in terms of solvent interactions with an ionic or radical-like transition state to the neglect of the possible contributions of ground-state factors. The importance of ground-state considerations in ion formation in certain solvolyses has, however, recently been amply demonstrated by Arnett and coworkersl. We wish to report results frcm'a study of a free radical dissociation in which both ground-and transition-state effects seem to require interpretation.
The reaction studied is the thermal decomposition of phenylazotriphenylmethane, I.
(c~H~)~C-N=N-C~H~ *
π SIMILAR VOLUMES
## Abstract A new soβcalled reactantβsolvent complex model is proposed to describe the effect of solvent on chain propagation in homopolymerization. It takes into account complex formation of both monomer and radical with solvent by equilibria. Evaluation methods presented permit to estimate the co
Rates and thermodynamic data have been obtained for the reversible self-termination reaction: 2k1 R' + R' G=-D Involving aromatic 2-(4'dimethylaminophenyl)indandione-1,3-y1 (I), 244'diphenylaminophenyl)indandione-1,3-y1 (II), and 2,6 di-tert-butyl-4-(p-phthalylvinyl)-phenoxyl (III) radicals in diffe