期刊文献+

微波固相法制备Mn(Salen)/Al-HMS催化剂 被引量:1

Mn(Salen)/Al-HMS Catalysts Prepared by Host-guest Interaction Under Microwave Irradiation
下载PDF
导出
摘要 采用微波固相法制备Mn(Salen)/A l-HMS催化剂,通过FT-IR、DR UV-V is和TG测试技术进行了表征。以苯乙烯为底物,PhIO为氧化剂进行环氧化反应,比较不同方法制备的催化剂的催化性能,通过考察催化剂制备过程中的微波辐射时间、氧化剂的用量及催化剂的重复使用对催化剂性能的影响规律。结果发现,微波固相法制备的Mn(salen)/A l-HMS-IP催化剂以苯乙烯为底物,PhIO为氧化剂,CH2C l2为溶剂在20℃下反应12 h,转化率可达74.6%,环氧苯乙烷选择率达94.8%,与常规方法制备的催化剂相比具有很好的催化活性。 Here we report a novel preparation method of Mn (Salen)/Al-HMS catalysts through host-guest interaction between Mn (Salen) complex and mesoporous Al-HMS under microwave irradiation (MWI). FT-IR, DR UV-Vis and TG measurement results indicate that Mn (Salen) complex could be successfully immobilized on mesoporous Al-HMS. Styrene epoxidation with PhIO as oxidant was carried out to test the effect of the catalyst prepared with different preparation methods on the catalytic activity and selectivity. It was found that the catalyst of Mn( Salen)/Al-HMS-IP1 shows a good conversion of styrene(74. 6% ) and the best selectivity for phenyloxirane(94. 8% ). Moreover, radiation time, quantity of oxidant and recycle times were investigated to investigate their effects on the catalytic performance.
出处 《应用化学》 CAS CSCD 北大核心 2006年第6期646-650,共5页 Chinese Journal of Applied Chemistry
基金 湖北省教育厅青年基金资助项目(Q20052700)
关键词 Mn(Salen)络合物 Al-HMS 微波辐射 苯乙烯 环氧化反应 Mn (Salen) complex, Al-HMS, microwave irradiation, styrene, epoxidation
  • 相关文献

参考文献13

  • 1Zhang W,Loebach J L,Wilson S R, et al. J Am Chem Soc[J].1990,112:2801 被引量:1
  • 2Irie R,Noda K,Ito Y, et al. Tetrahedron Lett[J].1990,31:7345 被引量:1
  • 3Minutolo F, Pini D, Salvadori P. Tetrahedron :Asymmetry[J].1996,7:2293 被引量:1
  • 4Kim G J,Kim S H. Catal Lett[J].1999,57:139 被引量:1
  • 5Ogunwumai S B,Bein T. J Chem Soc Chem Commun[J].1997:901 被引量:1
  • 6Sabater M J,Corma A,Domenech A, et al. J Chem Soc Chem Commum[J].1997:1285 被引量:1
  • 7Kim G J,Shin J H. Tetrahedron Lett[J].1999,40:6827 被引量:1
  • 8Donghong Y, Dulin Y. Microporous Mesoporous Mater[J].1998,24 : 123 被引量:1
  • 9Tanev P T, Pinnavaia T J. Science [J].1995,267:865 被引量:1
  • 10Boyapati M C,Mannepalli L K,Balagan B, et al. J Mol Catal A[J].2001,168:69 被引量:1

同被引文献14

  • 1Katsuki T. Adv Synth Catal[J] ,2002,344(2) :131. 被引量:1
  • 2McGarrigle E M, Gilheany D G. Chem Rev [ J ],2005,105 (5) : 1 563. 被引量:1
  • 3Bryliakov K P,Kholdeeva O A,Vanina M P,Talsi E P. J Mol Catal A:Chem[J] ,2002,178:47. 被引量:1
  • 4Song C E,Roh E J,Yu B M,Chi D Y,Kim S C,Lee K J. Chem Commun[J] ,2000,(7) :615. 被引量:1
  • 5Sabater M J,Corma A,Domenech A,Fornes V,Garcia H. Chem Commun[J] ,1997, (14) :1 285. 被引量:1
  • 6Piaggio P, Langham C, McMom P, Bethell D, Bulman-Page P C, Hancock F E, Sly C, Hutchings J. J Chem Soc Perkin Trans[ J] ,2000,2 : 143. 被引量:1
  • 7Fraile J M, Garcia J I, Massam J, Mayoral J A. J Mol Catal A : Chem [ J ], 1998,136 ( 1 ) :47. 被引量:1
  • 8Gil S, Gonzalez R, Mestres R, Sanz V, Zapater A. React Funct Polym [ J ], 1999,42 ( 1 ) :65. 被引量:1
  • 9FU Xiang-Kai(傅相锴),ZOU Kuang-Dong(邹矿东),FU Dan(富丹),GONG Rong-Feng(龚永锋).CN200610095053.1[P],2006. 被引量:1
  • 10Bai R F,FU X K,Bao H B,Ren W S. Catal Commun[J] ,2008,(9) :1 588. 被引量:1

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部