Some polystyrene-supported porphyrinatoiron( III) with different stereostructure were prepared using a new method and characterized by EA, UV-Vis,IR and EPR. Their catalytic activities in hydroxylation of cyclohexane with molecular oxygen have been found to be high compared with corresponding non-su
Hydroxylation of cyclohexane catalyzed by porphyrinatoiron(III) with molecular oxygen: the effect of the photochemical stability of porphyrinatoiron(III) in various solvents
β Scribed by Jin-Wang Huang; Wei-Zhuang Huang; Wen-Jie Mei; Jie Liu; Shu-Guang Hu; Liang-Nian Ji
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 117 KB
- Volume
- 156
- Category
- Article
- ISSN
- 1381-1169
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β¦ Synopsis
Ε½ .
Ε½ . The hydroxylation of cyclohexane catalyzed by 5,10,15,20-tetraphenylporphyrinatoiron III chloride TPPFeCl with molecular oxygen in various solvents have been preliminarily studied in the case when the catalytic reaction was not carried out in lighttight. The catalytic activity of TPPFeCl in various solvents was found to increase in the following order: acetone-benzene-methyl-cyanide, which is consistent with the order of the photochemical stability of TPPFeCl in various solvents. It seems these results are helpful to the choice of solvents in the research of the model of cytochrome P450.
π SIMILAR VOLUMES
Three iron(III)-metal-free porphyrin dimers linked covalently with a flexible butoxy chain at the paru position of the two phenyl rings have been prepared and characterized. The hydroxylation of cyclohexane catalyzed by these dimers with molecular oxygen under mild condition has been studied prelimi