The activation of dioxygen, at ambient conditions, by dimeric copper acetate complexes incorporated in molecular sieves Y, MCM-22 and VPIJ, in the oxidation of phenols to ortho diphenols and diphenols to o-quinones is reported. L-tyrosine is oxidised to L-DOPA, phenol to catechol, catechol to ortho
β¦ LIBER β¦
Kinetic studies of the activation of dioxygen by a series of copper(I)-complexes
β Scribed by M. Becker; S. Schindler
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 43 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0162-0134
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Stabilization of the bis(ΞΌ-oxo)dicopper(III) intermediate is achieved by using a bidentate N-donor ligand with pendent indole rings: N,N-bis[(3-indolyl)methyl]-N-[(2'-pyridyl)methyl]amine (BIP). The intermediate decomposes to give products arising from N-dealkylation and a product with a spiro ring