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Journal ArticleDOI

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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Journal ArticleDOI

2,3,7,8,12,13,17,18‐Octafluoro‐5,10,15,20‐Tetraphenylporphyrin: First Synthesis and X‐Ray Crystal Structure of the ZnII Complex

TL;DR: In this article, a wide range of β-octafluoro-meso-arylated porphyrins, a new class of highly electron-deficient ligands, are potentially accessible from 3,4-difluoropyrrole, thus opening the door to efficient and robust oxidation catalysts.
Journal ArticleDOI

New manganese β-polynitroporphyrins as particularly efficient catalysts for biomimetic hydroxylation of aromatic compounds with H2O2

TL;DR: A series of Mn porphyrins bearing one to eight β-nitro substituents were synthesized in high yield in three steps by using a new general method for selective nitration of a ============Zn(meso-tetraarylporphyrin) series exhibits a wide span of Mn(III)/Mn(II) redox potential from −290 to + 1150 mV.
Journal ArticleDOI

Hydrocarbon oxidation with iodosylbenzene catalysed by the sterically hindered iron(III) 5-(pentafluorophenyl)-10,15,20-tris(2,6-dichlorophenyl)porphyrin in homogeneous solution and covalently bound to silica

TL;DR: A sterically hindered iron porphyrin has also been covalently bound by nucleophilic aromatic substitution to aminopropylated silica as mentioned in this paper, which is also stable towards oxidation but is less reactive than its homogeneous analogue.
Journal ArticleDOI

Synthesis and characterization of mononuclear ruthenium(III) pyridylamine complexes and mechanistic insights into their catalytic alkane functionalization with m-chloroperbenzoic acid.

TL;DR: These complexes act as effective catalysts for alkane functionalization in acetonitrile with m-chloroperbenzoic acid (mCPBA) as terminal oxidant at room temperature and can be altered significantly by the electronic effects of substituents on TPA ligands in terms of initial rates and turnover numbers.
Journal ArticleDOI

A Porphyrin Embedded in DNA

TL;DR: In this paper, the first porphyrin−nucleic acid conjugates bearing the porphrin embedded in the backbone of DNA were synthesized by automated solid-phase synthesis using a dimethoxytrityl-protected porphryin phosphoramidite and standard DNA building blocks.
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