Efficient and selective oxidation of methyl substituted cycloalkanes by heterogeneous methyltrioxorhenium-hydrogen peroxide systems

被引:27
作者
Bianchini, Gianluca
Crucianelli, Marcello
Canevali, Carmen
Crestini, Claudia
Morazzoni, Franca
Saladino, Raffaele
机构
[1] Univ Aquila, Dipartimento Chim Ingn Chim & Mat, I-67010 Coppito, AQ, Italy
[2] Univ Studi Milano Bicocca, Dipartimento Sci Mat, I-20125 Milan, Italy
[3] Univ Roma Tor Vergata, Dept Chim & Tecnol, Rome, Italy
[4] Univ Tuscia, Dipartimento Agrobiol & Agrochim, I-01100 Viterbo, Italy
关键词
heterogeneous catalysis; methyltrioxorhenium; radical reactions; EPR spectroscopy;
D O I
10.1016/j.tet.2006.10.013
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Polymer-supported methyltrioxorhenium (MTO) systems are efficient catalysts for the oxidative functionalisation of cyclohexane and cyclopentane, derivatives with H2O2 as oxygen donor. Using poly (4-vinyl)pyridine and poly(4-vinyl)pyridine-N-oxide as MTO supports, cycloalkanol, cycloalkanediol, cycloalkanone and omega-hydroxy methyl ketone derivatives were obtained in different yields depending on the experimental conditions. Interestingly, cycloalkane dimers were selectively recovered in acceptable to good yields when the oxidation was performed with polystyrene-microencapsulated MTO catalyst. The EPR investigation suggests that the homolytic cleavage of the CH3-Re bond with formation of CH3 center dot radicals occurs inside the polystyrene capsule, indicating a possible role of methyl radical in the cycloalkane dimerisation pathway. (c) 2006 Published by Elsevier Ltd.
引用
收藏
页码:12326 / 12333
页数:8
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