Oxidative catalysis by Mn4O46+ cubane complexes

被引:59
作者
Carrell, TG [1 ]
Cohen, S [1 ]
Dismukes, GC [1 ]
机构
[1] Princeton Univ, Dept Chem, Princeton, NJ 08544 USA
基金
美国国家卫生研究院;
关键词
oxidation; polynuclcar manganese complexes; alkyl hydroperoxides;
D O I
10.1016/S1381-1169(02)00139-5
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The oxidation of a variety of substrates (thioethers, hydrocarbons, alkenes, benyzl alcohol and benzaldehyde) by (BuOOH)-Bu-t catalyzed by Mn4O4(O2PPh2)(6) (1) and Mn4O4(O2P(p-MePh)(2))(6) (2) is reported. These reactions illustrate the first examples of oxidative catalysis using a manganese-oxo complex with a Mn4O4 cubane core. These uncharged complexes contain Mn ions in a mixed valence oxidation state, formally Mn-4(2III, 2IV), and are bridged by bulky diphenylphosphinate chelates across each of the six faces of the cube. Using this system, methyl phenyl sulfide is selectively mono-oxygenated to methyl phenyl sulfoxide with high catalytic efficiency, and no evidence for further oxidation to the thermodynamically preferred sulfone. Toluene is oxidized to a mixture of benzyl alcohol, benzaldehyde, and benzoic acid with high catalytic efficiencies. Lower catalytic efficiencies are observed in the oxidation of styrene to a mixture of styrene oxide and benzaldehyde, of cyclohexene to a mixture of cyclohexene oxide, 2-cyclohexen-1-ol, and 2-cyclohexen-1-one, and of cyclohexane to a mixture of cyclohexanol and cyclohexanone. The observed product distribution from the oxidation of hydrocarbons has the characteristics of a free radical-based oxidation mechanism. However, the sulfoxidation and epoxidation activity of the 1/(BuOOH)-Bu-t system, as well as the observed steric preferences for less congested substrates, suggest that a metal-oxo centered oxidation mechanism is active in the reactions studied here. An intermediate species, characterized by a UV-VIS band centered at 6 10 nm is observed in all reaction mixtures, and forms upon reaction of 1 or 2 with (BuOOH)-Bu-t. Preliminary evidence suggests this reactive intermediate may correspond to a Mn(V)=O species. Kinetic studies suggest two pathways for oxidation: one involving an oxygen atom transfer (two-electron branch), and the other involving a hydrogen atom abstraction (one-electron branch). (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:3 / 15
页数:13
相关论文
共 44 条
[1]   THE SELECTIVE FUNCTIONALIZATION OF SATURATED-HYDROCARBONS - GIF CHEMISTRY [J].
BARTON, DHR ;
DOLLER, D .
ACCOUNTS OF CHEMICAL RESEARCH, 1992, 25 (11) :504-512
[2]   'Oxo-hydroxo tautomerism' as useful mechanistic tool in oxygenation reactions catalysed by water-soluble metalloporphyrins [J].
Bernadou, J ;
Meunier, B .
CHEMICAL COMMUNICATIONS, 1998, (20) :2167-2173
[3]   Synthesis, characterization, and reactivity of ferrous and ferric oxo/peroxo pivalate complexes in relation to Gif-type oxygenation of substrates [J].
Çelenligil-Çetin, R ;
Staples, RJ ;
Stavropoulos, P .
INORGANIC CHEMISTRY, 2000, 39 (25) :5838-5846
[4]   Formation and role of cobalt and manganese cluster complexes in the oxidation of p-xylene [J].
Chavan, SA ;
Halligudi, SB ;
Srinivas, D ;
Ratnasamy, P .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2000, 161 (1-2) :49-64
[5]   Enantioselective sulfoxidation as a probe for a metal-based mechanism in H2O2-dependent oxidations catalyzed by a diiron complex [J].
Duboc-Toia, C ;
Ménage, S ;
Ho, RYN ;
Que, L ;
Lambeaux, C ;
Fontecave, M .
INORGANIC CHEMISTRY, 1999, 38 (06) :1261-1268
[6]   CARBON HYDROGEN ACTIVATION CHEMISTRY - HYDROXYLATION OF C2, C-3, AND CYCLO-C6 HYDROCARBONS BY MANGANESE CLUSTER CATALYSTS WITH A MONO-OXYGEN TRANSFER REAGENT [J].
FISH, RH ;
FONG, RH ;
VINCENT, JB ;
CHRISTOU, G .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1988, (22) :1504-1506
[7]   ELECTRONIC-STRUCTURE AND SPECTROSCOPY OF MANGANESE CATALASE AND DI-MU-OXO [MN(III)MN(IV)] MODEL COMPLEXES [J].
GAMELIN, DR ;
KIRK, ML ;
STEMMLER, TL ;
PAL, S ;
ARMSTRONG, WH ;
PENNERHAHN, JE ;
SOLOMON, EI .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (06) :2392-2399
[8]  
Gross Z, 2000, ANGEW CHEM INT EDIT, V39, P4045, DOI 10.1002/1521-3773(20001117)39:22<4045::AID-ANIE4045>3.0.CO
[9]  
2-P
[10]   Detection and characterization of an oxomanganese(V) porphyrin complex by rapid-mixing stopped-flow spectrophotometry [J].
Groves, JT ;
Lee, JB ;
Marla, SS .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (27) :6269-6273