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

被引:52
作者
Bartoli, JF [1 ]
Mouries-Mansuy, V [1 ]
Le Barch-Ozette, K [1 ]
Palacio, M [1 ]
Battioni, P [1 ]
Mansuy, D [1 ]
机构
[1] Univ Paris 05, UMR 8601, F-75270 Paris 06, France
关键词
D O I
10.1039/b001776k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of Mn porphyrins bearing one to eight beta-nitro substituents were synthesized in high yield in three steps by using a new general method for selective nitration of a Zn(meso-tetraarylporphyrin); this Mn porphyrin series exhibits a remarkably wide span of Mn(III)/Mn(II) redox potentials from -290 to + 1150 mV (vs. SCE), and the Mn porphyrins bearing one to five beta-nitro groups are particularly good catalysts for hydroxylation of aromatic compounds with H2O2, with yields up to 98, 83, 80 and 12%, respectively for anisole, naphthalene, acetanilide and ethylbenzene.
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页码:827 / 828
页数:2
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