期刊文献+

Suzuki Reactions in Water Catalyzed by an Active and Reus- able PMO-Type Pd(ll) Organometal Catalyst with Cage-Like Mesoporous Structure

Suzuki Reactions in Water Catalyzed by an Active and Reus- able PMO-Type Pd(ll) Organometal Catalyst with Cage-Like Mesoporous Structure
原文传递
导出
摘要 A novel Pd(ll) organometal catalyst with three-dimensional (3D) cage-like la3d cubic mesoporous structure and high surface area was prepared. In comparison with the corresponding catalyst with two-dimensional (2D) P6mm hexagonal mesoporous structure, the as-prepared catalyst exhibited higher activities in the water-medium Suzuki coupling reactions owing to the diminished diffusion limit. It showed comparable efficiencies with the Pd(PPh3)2C12 homogeneous catalyst and could be easily recycled and reused for five times without significant loss of activity. A novel Pd(ll) organometal catalyst with three-dimensional (3D) cage-like la3d cubic mesoporous structure and high surface area was prepared. In comparison with the corresponding catalyst with two-dimensional (2D) P6mm hexagonal mesoporous structure, the as-prepared catalyst exhibited higher activities in the water-medium Suzuki coupling reactions owing to the diminished diffusion limit. It showed comparable efficiencies with the Pd(PPh3)2C12 homogeneous catalyst and could be easily recycled and reused for five times without significant loss of activity.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2012年第9期2151-2157,共7页 中国化学(英文版)
关键词 Pd(I1) organometal catalyst PMO cage-like bicontinuous cubic mesostructure water-medium clean organic reactions the Suzuki reaction Pd(I1) organometal catalyst, PMO, cage-like bicontinuous cubic mesostructure, water-medium clean organic reactions, the Suzuki reaction
  • 相关文献

参考文献49

  • 1Comprehensive Organic Synthesis, Eds.: Trost, B. M.; Fleming, I., Pergamon Press, Oxford, 1991, pp. 481 520.
  • 2Miyaura, N.; Yamada, K.; Suzuki, A. Tetrahedron Lett. 1979, 36, 3437.
  • 3Miyaura, N. Top. Curr. Chem. 2002, 219, 11.
  • 4Lv, B.; Fu, C. L.; Ma, S. M. Tetrakedron Lett. 2010, 51, 1284.
  • 5Handbook of Organopalladium Chemistry for Organic Synthesis Ed.: Negishi, E. I., John Wiley & Sons, lnc, New York, 2004.
  • 6Metal-Catalyzed Cross-Coupling Reactions, Eds.: De Meijere, A.; Diederich, F., John Wiley & Sons, |nc, New York 2004.
  • 7Prashad, M. Top. Organomet. Chem. 2004, 6, 181.
  • 8Sheldon, R.; Arends, l.; Hanefeld, U. Green Chemistry and Catalv- sis, Wiley-VCH, Weinheim, Germany, 2007.
  • 9Li, J. H.; Hu, X. C.; Liang, Y.; Xie, Y. X. Tetrahedron 2006, 62, 31.
  • 10Mu, B.; Li, J. Y.; Han, Z. X.; Wu, Y. J. J. Organometal. Chem. 2012, 700, 117.

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