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Metalloporphyrins as versatile catalysts for oxidation reactions and oxidative DNA cleavage

Bernard Meunier
- 01 Sep 1992 - 
- Vol. 92, Iss: 6, pp 1411-1456
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This article is published in Chemical Reviews.The article was published on 1992-09-01. It has received 1930 citations till now.

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Selective oxidation of styrene to 1,2-epoxyethylbenzene by hydrogen peroxide over heterogeneous phosphomolybdic acid supported on ionic liquid modified MCM-41

TL;DR: In this article, a 1,2-epoxyethylbenzene catalyzed by phosphomolybdic acid supported on ionic liquid modified MCM-41 using hydrogen peroxide as oxidant.
Journal ArticleDOI

Insight into ultrasound-mediated reactive oxygen species generation by various metal-porphyrin complexes

TL;DR: The cytotoxicity results reported herein, which are mirrored by ex‐cellulo data, confirm that the type of ROS generation achieved by the US activation of intracellular porphyrins is pivotal to the effectiveness of cancer cell killing.
Journal ArticleDOI

Rapid and efficient oxidation of Hantzsch 1,4-dihydropyridines with sodium periodate catalyzed by manganese (III) Schiff base complexes.

TL;DR: The Mn(III)-salophen/NaIO4 catalytic system converts 1,4-dihydropyridines to their corresponding pyridine derivatives at room temperature in a 1:1, CH3CN/H2O mixture.
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Effects of humic substances on the pattern of oxidation products of pentachlorophenol induced by a biomimetic catalytic system using tetra(p-sulfophenyl)porphineiron(III) and KHSO5.

TL;DR: In the presence of humic substances (HSs), the oxidative conversion of pentachlorophenol (PCP) was found to be efficiently catalyzed by tetra(p-sulfophenyl)porphineiron(III) (Fe(III)-TPPS) using KHSO5 as an oxygen donor.
Journal ArticleDOI

Hydrogen Peroxide Oxidation of Mustard-Model Sulfides Catalyzed by Iron and Manganese Tetraarylporphyrines. Oxygen Transfer To Sulfides versus H2O2 Dismutation and Catalyst Breakdown

TL;DR: It is shown that the efficiency of the oxygen transfer is related not only to the rate constant of the dismutation route but also to the concentration of the active metal-oxo intermediate, most likely a perferryl or permanganyl species, i.e., to the rates of its formation.
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