中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Hydrogenation of nitrobenzene, cyclohexanone and octene catalyzed by silica-supported starch-L-glutamic acid-Fe complex

文献类型:期刊论文

作者Liu, HW; Huang, K; Mi, JD; Jia, Y; Huang, MY; Jiang, YY
刊名POLYMERS FOR ADVANCED TECHNOLOGIES
出版日期2003-03-01
卷号14期号:3-5页码:355-359
关键词Starch Glutamic Acid Fe Complex Catalyst Hydrogenation Nitrobenzene
ISSN号1042-7147
DOI10.1002/pat.320
英文摘要A new polymer-base metal complex, silica-supported starch-L-glutamic acid-Fe complex (SiO2-ST-Glu-Fe) has been prepared by a simple method. Starch was reacted with L-glutamic acid in the presence of silica to give a ligand SiO2-ST-Glu, then this was reacted with FeCl3.6H(2)O to form the Fe complex (SiO2-ST-Glu-Fe). The complex has been found to be able to catalyze the hydrogenation of nitrobenzene to give aniline in 100% yield, cyclohexanone to give cyclohexanol in 93% yield and octene to give octane in 84% yield at 45degreesC and under atmospheric pressure. Experimental data show that the catalyst was very stable and could be reused without any noticeable change in its catalytic activity. Copyright (C) 2003 John Wiley Sons, Ltd.
语种英语
WOS记录号WOS:000182654500032
出版者JOHN WILEY & SONS LTD
源URL[http://ir.iccas.ac.cn/handle/121111/81077]  
专题中国科学院化学研究所
通讯作者Liu, HW
作者单位Chinese Acad Sci, Inst Chem, Beijing 100080, Peoples R China
推荐引用方式
GB/T 7714
Liu, HW,Huang, K,Mi, JD,et al. Hydrogenation of nitrobenzene, cyclohexanone and octene catalyzed by silica-supported starch-L-glutamic acid-Fe complex[J]. POLYMERS FOR ADVANCED TECHNOLOGIES,2003,14(3-5):355-359.
APA Liu, HW,Huang, K,Mi, JD,Jia, Y,Huang, MY,&Jiang, YY.(2003).Hydrogenation of nitrobenzene, cyclohexanone and octene catalyzed by silica-supported starch-L-glutamic acid-Fe complex.POLYMERS FOR ADVANCED TECHNOLOGIES,14(3-5),355-359.
MLA Liu, HW,et al."Hydrogenation of nitrobenzene, cyclohexanone and octene catalyzed by silica-supported starch-L-glutamic acid-Fe complex".POLYMERS FOR ADVANCED TECHNOLOGIES 14.3-5(2003):355-359.

入库方式: OAI收割

来源:化学研究所

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