Photoinduced reactions. XXX. Hydrogen abstraction from a phenol by singlet oxygen
β Scribed by Teruo Matsuura; Naoki Yoshimura; Akira Nishinaga; Isao Saito
- Publisher
- Elsevier Science
- Year
- 1969
- Tongue
- French
- Weight
- 131 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
In a previous paper of this series, it has been shown that several hindered phenols undergo dye-sensitized photooxygenation to give various oxidation products. For example, 2,6di-t-butylphenol (l~ yielded 2,6-di-t-butyl-p-benzoquinone (2~ and 3,5,3',5'-tetra-t-butyl-4,4'-diphenoquinone (~ besides some polymers.
We suggested that, as shown in Scheme i,
π SIMILAR VOLUMES
An important step in the initial oxidation of hydrocarbons at low to intermediate temperatures is the abstraction of H by hydroperoxyl radical (HO(2)). In this study, we calculate energy profiles for the sequence: reactant + HO(2) β [complex of reactants] β transition state β [complex of products] β
The homolysis of a Co-C bond accompanied by hydrogen abstraction from environmental molecules giving rise to the new Co-C bond formation with the molecules is of particular interest in connection with the reaction mechanism of the vitamin B12 dependent dehydrase.'