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Alkane hydroxylation reactions catalysed by binuclear manganese and iron complexes

✍ Scribed by David Tetard; Jean-Baptiste Verlhac


Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
773 KB
Volume
113
Category
Article
ISSN
1381-1169

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✦ Synopsis


Binuclear manganese(III/IV)

or iron(III/III) complexes efficiently functionalize cyclohexane using hydroperoxides or peracids as oxidants. A mechanistic study clearly demonstrate the role of dioxygen gas in these hydroxylation reactions. Moreover, it was demonstrated that the cleavage of the peroxy bond occurred mainly by homolysis.


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Higher alkanes (cyclohexane, n-pentane, n-heptane, methylbutane, 2-and 3methylpentanes, 3-methylhexane, cis-and trans-deealins) are oxidized at 20 Β°C by H202 in air in acetonitrile (or nitromethane) solution in the presence of the manganese(IV) salt [L2Mn203](PF6)2 (L = 1,4,7-trimethyl-1,4-7-triazac