Acta Chimica Sinica ›› 2008, Vol. 66 ›› Issue (9): 1009-1014.     Next Articles

Original Articles

Rh(PPh3)3Cl/有机融盐催化烯烃硅氢加成反应

厉嘉云,彭家建,吴慧,白赢,邱化玉*,蒋剑雄,来国桥*   

  1. (杭州师范大学有机硅化学及材料技术教育部重点实验室 杭州 310012)
  • 投稿日期:2007-09-27 修回日期:2007-12-05 发布日期:2008-05-14
  • 通讯作者: 来国桥

Hydrosilylation of Alkenes Catalyzed with Rh(PPh3)3Cl/Organic Molten Salt

LI Jia-Yun PENG Jia-Jian WU Hui BAI Ying QIU Hua-Yu* JIANG Jian-Xiong LAI Guo-Qiao*   

  1. Key Laboratory of Organosilicon Chemistry and Material Technology of Ministry of Education, Hangzhou Normal University, Hangzhou 310012)
  • Received:2007-09-27 Revised:2007-12-05 Published:2008-05-14
  • Contact: LAI Guo-Qiao

The activity and selectivity influenced by Rh(PPh3)3Cl/dialkylimidazolium hexafluorophosphate or N-alkylpyridinium hexafluorophosphate have been investigated in the hydrosilylation of olefin with triethylsilane. It was found that both conversion and selectivity to β-product could be improved, but the selectivities to α-product and unsaturated product decreased by using this catalyst. The Rh(PPh3)3Cl/C16PyPF6 exhibited the highest selectivity to β-product in the hydrosilylation of styrene by triethylsilane. The conversion of styrene was 95.7%, the selectivity to β-product was 87.8%, the selectivity to α-product was 0.001%, and the selectivity to unsaturated product was 9.2%. At the same time, this catalyst might be reused more than seven times without noticeable loss of its catalytic activity.

Key words: Rh(PPh3)3Cl, dialkylimidazolium hexafluorophosphate, N-alkylpyridinium hexafluorophosphate, hydrosilylation, triethylsilane