Catalytic activity of aminopropyl xerogels in the selective synthesis of (E)-nitrostyrenes from nitroalkanes and aromatic aldehydes

被引:88
|
作者
Sartori, G
Bigi, F
Maggi, R
Sartorio, R
Macquarrie, DJ
Lenarda, M
Storaro, L
Coluccia, S
Martra, G
机构
[1] Clean Synth Methodol Grp, Dipartimento Chim Organ & Ind Univ, I-43100 Parma, Italy
[2] Univ York, Dept Chem, York YO10 5DD, N Yorkshire, England
[3] Univ Ca Foscari, Dipartimento Chim, INSTM, UdR Venezia, I-30174 Mestre Venezia, Italy
[4] Univ Turin, IFM, Dipartimento Chim, I-10125 Turin, Italy
关键词
aminopropyl silica; base catalyst; nitroaldol condensation; nitroalkene; hybrid organic-inorganic material; infrared;
D O I
10.1016/j.jcat.2003.11.016
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
Various aminopropyl-functionalized silicas (APS) were prepared by the sol-gel technique using different tetraethyl orthosilicate/aminopropyltriethoxysilane (TEOS/ATS) ratios and tested as base catalysts for the nitroaldol reaction. The solids were fully characterized. It was proved that the amount of organic component strongly influences the composition and textural properties of the hybrid organic-inorganic materials. In particular, when ATS was increased to more than 40%, pore volume collapse was observed and a significant decrease in interaction with benzaldehyde reagent was revealed by FT-IR. Catalytic activity in the nitroaldol reaction was correlated with chemical composition and textural properties, suggesting that the catalyst efficiency depends on accessibility to the catalytic sites. In all cases, (E)nitrostyrene was selectively obtained. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:410 / 418
页数:9
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