Oxidation of 2,6-di-tert-butylphenol with polymer anchored molybdenyl and vanadyl complexes
β Scribed by Rita Pathak; G.N. Rao
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- English
- Weight
- 79 KB
- Volume
- 130
- Category
- Article
- ISSN
- 1381-1169
No coin nor oath required. For personal study only.
β¦ Synopsis
Ε½ t . Ε½ . The oxidation of 2,6-di-tert-butylphenol with tert-butylhydroperoxide Bu O H has been studied using polymer XAD 2 4
anchored salicylaldoxime, 1,3-propylene-bis-salicylaldimine and o-phenylene-bis-salicylaldimine complexes of molybdenum and vanadium in acetonitrile. The predominant products formed in the oxidation reactions were 2,6-di-tert-butylben-Ε½ .
X X
Ε½ . zoquinone BQ and 3,3 -5,5 -tetra-tert-butyldiphenoquinone dPQ , whereas with some only 2,6-di-tert-butylbenzoquinone was formed. This is the first reported use of polymer anchored molybdenyl and vanadyl complexes in selective oxidation of 2,6-di-tert-butylphenol. Solvent plays an important role in this reaction. The effects of varying the ligand, metal and the support on the catalytic activity in the oxidation of 2,6-di-tert-butylphenol have been studied. With polymer anchored Ε½ . MoO salpen , 81% of 2,6-di-tert-butylbenzoquinone was formed from 2,6-di-tert-butylphenol. q 1998 Elsevier Science 2 B.V.
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