Methanolysis of styrene oxide catalysed by a highly efficient zirconium-doped mesoporous silica

被引:35
作者
Barreca, Davide
Copley, Mark P. [1 ]
Graham, Andrew E.
Holmes, Justin D.
Morris, Michael A.
Seraglia, Roberta
Spalding, Trevor R.
Tondello, Eugenio
机构
[1] Univ Coll Cork, Dept Chem, Mat Sect, Cork, Ireland
[2] Univ Coll Cork, Supercrit Fluid Ctr, Cork, Ireland
[3] Univ Padua, ISTM, CNR, Padua, Italy
[4] Univ Padua, INSTM, Padua, Italy
[5] Univ Coll Swansea, Dept Chem, Swansea SA2 8PP, W Glam, Wales
[6] CN ISTM, I-35127 Padua, Italy
关键词
mesoporous silica; zirconium; styrene oxide; methanolysis; regeneration;
D O I
10.1016/j.apcata.2006.02.034
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
Highly ordered zirconium doped hexagonal mesoporous silicas with Si/Zr ratios of 40:1 and 80:1 have been used as solid acid catalysts for the methanolysis of styrene oxide in a single-mode microwave reactor. The catalysts demonstrated excellent substrate conversion, high product selectivities and were shown to remain highly active for several reaction cycles. The catalyst was regenerated by microwave irradiation in methanol. The effects of concentration of zirconium dopant and reaction time were studied. Products of the reaction were identified by a combination of GC-MS and H-1 NMR as 2-methoxy-2-phenylethanol (1), phenyl-acetaldehyde (2), phenylacetaldehyde dimethyl acetal (3) and 1-(1-methoxy-2-(phenethyloxy)ethyl)benzene (4). The relative amounts of these products depended on the zirconium concentration and the reaction time. Thus, with 40:1 Si:Zr catalyst, compounds (1) (93%), (2) (5%) and (3) (2%) were produced after 5 min reaction but only (1) (93%) and (3) (7%) were observed after 10 min. (c) 2006 Elsevier B.V. All rights reserved.
引用
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页码:14 / 20
页数:7
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