期刊文献+

MTO/离子液体催化环氧化环己烯的研究

MTO catalyzed epoxidation of cyclohexene in ionic liquids
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摘要 分别以合成的4种离子液体为反应溶剂,CH3ReO3为催化剂,UHP为氧化剂,对环己烯进行环氧化催化.实验结果表明,在4种离子液体为溶剂的体系中,其中[emi]SE离子液体为反应溶剂的催化效果最好.在MTO/[emi]SE催化环氧化环己烯的体系中,最优催化反应条件为:n(催化剂):n(底物):n(氧化剂)=2:100:200,离子液体1.2 ml. The catalytic system was established by using MTO as catalyst,UHP as oxidant,and four kinds of ionic liquids as reaction solvents,and the properties of catalytic epoxidation for cyclohexene were investigated. The results indicated that it is an effective system for epoxidetion of cyclohexene with better activities at the room temperature. The epoxidation is the best when using [emi]SE ionic liquid as solvent,the best reaction conditions of olefins at room temperature are by orthogonal experiment:2 mmol cyclohexene as substrate, the catalyst : substrate: oxidant 2 : 100 : 200, ionic liquid 1.2 ml.
出处 《材料研究与应用》 CAS 2009年第3期183-186,共4页 Materials Research and Application
基金 国家自然科学基金项目(NSFC20671047)
关键词 离子液体 甲基三氧化铼(MTO) 环己烯 催化 环氧化 ionic liquid MTO cyclohexene catalyze epoxidation
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参考文献15

  • 1HERRMANN W A, KUCHLER J G, FELIXBERGE J K,etal. Methylrhenium oxides: synthesis from R2O7 and catalytic activity in olefin metathesis[J]. Angew Chem Int Ed Engl, 1988,27(3) .. 394-396.
  • 2任译,吴云东,田安民.新型高效催化剂—甲基三氧化铼(MTO)的研究进展[J].有机化学,2001,21(6):413-419. 被引量:8
  • 3KUHN F E, SCHERBAUM A, HERRMANN W A. Methyltrioxorhenium and its applications in olefin oxidation, metathesis and aldehyde olefinatio[J]. Org Chem, 2004, 689 : 4149-4164.
  • 4PEDRO F M, HIRNER S, KUHN F E. Catalytic ketone olefination with methyltrioxorhenium[J]. Tetrahedron Letters, 2005,46 : 7777-7779.
  • 5ROMAO C C,KUHN F E, HERRMANN W A. Rtheniurn(Ⅵ)oxo and imido complexes: synthesis, structures, and applications[J]. Chem Rev, 1997,97: 3197-3246.
  • 6ESPENSON J H. Atom-transfer reactions catalyzed by methyltrioxorhenium(Ⅶ)-mechanisms and applications [J]. Chem Commun, 1999:479-488.
  • 7HERRMANN W A,FISCHER R W, MARZ D W,et al. Methyltrioxorhenium as catalyst for olefin oxidation[J]. Chem Int Ed, 1991,30:1638-1641.
  • 8HERRMANN W A, FISCHER R W, RAUCH M U, etal. Ylrheniumoxides as homogeneous epoxidation catalysts: activity, selectivity, stability, dactivation [J ]. Mol Catal A: Chem, 1994,86:243-266.
  • 9KUHN F E,SANTOS A M. Rional-bpyramidal lwis bse aducts of mthyltrioxorhenium (Ⅶ) and teir bsperoxo cngeners: caracterization, aplication in ctalytic eoxidation,and dnsity fnctional mchanistic sudy[J]. Chem Eur J, 1999,5: 3603.
  • 10SANTOS A M,KUHN F E. Syntheses and characterisation of methyltrioxorhenium adduets of low-valence organometallie lewis bases [J]. Chem Soc, 2000, 35:3570.

二级参考文献17

  • 1Qian Y L,金属有机化学与催化,1997年,1页
  • 2Zhu Z,J Am Chem Soc,1996年,118卷,9901页
  • 3Zhu Z,J Org Chem,1996年,61卷,324页
  • 4Murray R W,Tetrahedron Lett,1996年,37卷,805页
  • 5Zhu Z,J Org Chem,1995年,61卷,324页
  • 6Zhu Z,J Org Chem,1995年,60卷,7728页
  • 7Murray R W,Tetrahedron Lett,1995年,36卷,6415页
  • 8Adam W,J Org Chem,1994年,59卷,8281页
  • 9Herrmann W A,Angew Chem Int Ed Engl,1991年,30卷,1641页
  • 10Huang R,J Org Chem,1999年,64卷,6374页

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