期刊文献+

木质素-四乙烯五胺负载钯配合物的制备及对Suzuki反应的催化性能 被引量:3

Synthesis of Lignin-tetraethylenepentamine Palladium Complex and Its Catalytic Properties for Suzuki Reaction
下载PDF
导出
摘要 采用较温和的Mannich反应制得了木质素-四乙烯五胺,并以其为载体通过简单的方法制备了木质素-四乙烯五胺负载钯催化剂。利用TG、DTA和XPS等测试技术对其结构进行了表征。该催化剂对碘苯与四苯硼钠的Suzuki反应有较好的催化活性,在80℃下空气氛围中反应8h,以V(DMF)∶V(H2O)=2∶1混合液为溶剂,NaHCO3为碱时,反应产率高达90.2%。催化剂可以通过简单的方法回收但重复使用性能有一定下降,重复使用4次后产率降至31.3%。 Lignin-tetraethylenepentamine was synthesized from Lignin and tetraethylenepentamine( TEPA) with formaldehyde as a cross-linking agent by Mannich reaction. The prepared complex was used as a matrix to support palladium chloride. Lignin-TEPA-Pd complex was characterized by XPS,TG and DTA,which was an efficient catalyst for the Suzuki reaction of iodobenzene with sodium tetra-phenylboron. The yield of the product was up to 90. 2% when the reaction was carried out at 80 ℃ in air for 8 h with V( DMF) ∶ V( H2O) = 2∶1 mixture as the solvent and NaHCO3 as the base. The catalyst could be separated easily,but the yield of product decreased to 31. 3% after 4 times reusage.
出处 《应用化学》 CAS CSCD 北大核心 2010年第7期787-791,共5页 Chinese Journal of Applied Chemistry
基金 河南省自然科学基金资助项目(611020500)
关键词 木质素 负载型催化剂 SUZUKI反应 Lignin palladium supported catalyst Suzuki reaction
  • 相关文献

参考文献20

  • 1Trost B M,Keinan E.J Am Chem Soc[J].1978,100(24):7779.
  • 2Trost B M,Warner R W.J Am Chem Soc[J].1982,104(22):6112.
  • 3Lu G,Franz R,Zhang Q,Xu Y.Tetrahedron Lett[J].2005,46(24):4255.
  • 4Leadbeater N E,Marco M.J Org Chem[J].2003,68(14):5660.
  • 5Yan J,Zhou Z S.Chinese Chem Lett[J].2006,17(4):473.
  • 6周少林,徐利文,夏春谷,李经纬,李福伟.Suzuki偶联反应的最新研究进展[J].有机化学,2004,24(12):1501-1512. 被引量:31
  • 7Bellina F,Carpita A,Rossi R.Synthesis[J].2004,(15):2419.
  • 8Suzuki A.Proc Jpn Acad Ser B[J].2004,80(8):359.
  • 9Felpin F X,Ayad T,Mitra S.Eur J Org Chem[J].2006:2679.
  • 10Ping H,Haswell S J,Fletcher P D I.Appl Catal A:Gen[J].2004,274:111.

二级参考文献92

  • 1Castanet, A.; Colobert, F.; Broutin, P.; Obringer, M.Tetrahedron : Asymmetry 2002, 13, 659.
  • 2Yin, J.; Buchwald, S. L. J. Am. Chem. Soc. 2000, 122,12051.
  • 3Prickett, M. P. ; Singh, G. ; Vankayalapati, H. Tetrahedron Lett. 2000, 41, 2987.
  • 4Sutton, A. E. ; Clardy, J. Tetrahedron Lett. 2001, 42, 547.
  • 5Wang, W. ; Zhang, J. ; Xiong, C. ; Hruby, V. J. Tetrahedron Lett. 2002, 43, 2137.
  • 6Chiellini, G. ; Nguyen, N. H. ; Apriletti, J. W. ; Baxter, J.D. ; Scanlan, T. S. Bioorg. Med. Chem. 20112, 10, 333.
  • 7Yoburn, J. ; Van Vranken, D. L. Org. Lett. 20113, 5, 2817.
  • 8Gravett, E. C.; Hilton, P. J.; Jones, K.; Peron, J. M.Synlett 2003, 253.
  • 9Arterburn, J. B.; Bryant, B. K.; Chen, D. J. Chem.Commun. 2003, 1890.
  • 10Cossy, J. ; Belotti, D. ; Magner, A. Synkett 2003, 1515.

共引文献63

同被引文献20

引证文献3

二级引证文献8

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