Silica-immobilized N-hydroxyphthalimide:: An efficient heterogeneous autoxidation catalyst

被引:56
作者
Hermans, Ive
Van Deun, Jeroen
Houthoofd, Kristof
Peeters, Jozef
Jacobs, Pierre A.
机构
[1] Katholieke Univ Leuven, Ctr Catalysis & Surface Sci, B-3001 Heverlee, Belgium
[2] Katholieke Univ Leuven, Dept Chem, B-3001 Heverlee, Belgium
关键词
autoxidation; heterogeneous catalysis; immobilization; MAS-NMR; mechanism; NHPI; radicals;
D O I
10.1016/j.jcat.2007.06.025
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
Despite the potential of N-hydroxyphthalimide as a sustainable organocatalyst for autoxidations, recycling remains a largely unexplored but important topic. In this contribution, impregnation on silica is presented as a successful immobilization strategy. The activity of this catalyst during cyclohexane autoxidation is closely correlated with the support surface structure, as elucidated by Si-29 MAS NMR. It is found that sorption of byproducts is the main cause of deactivation such that only. silicas with a low number of residual hydroxyl groups result in stable catalytic systems. Nevertheless, even for active catalysts, a slight loss in activity can be observed on a first recycling. Fortunately, the catalytic activity remains steady in subsequent recycling runs, showing only negligible additional byproduct sorption. The reduced hydroperoxide and enhanced ketone yields afforded by this catalyst is explained in terms of the phthalimide-N-oxyl radical chemistry, whereby this nitroxyl radical efficiently converts hydroperoxide to ketone on abstraction of the alpha H-atom. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:204 / 212
页数:9
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