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Acta Chimica Sinica ›› 2008, Vol. 66 ›› Issue (9): 1009-1014. Next Articles
Original Articles
厉嘉云,彭家建,吴慧,白赢,邱化玉*,蒋剑雄,来国桥*
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LI Jia-Yun PENG Jia-Jian WU Hui BAI Ying QIU Hua-Yu* JIANG Jian-Xiong LAI Guo-Qiao*
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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
LI Jia-Yun PENG Jia-Jian WU Hui BAI Ying QIU Hua-Yu* JIANG Jian-Xiong LAI Guo-Qiao*. Hydrosilylation of Alkenes Catalyzed with Rh(PPh3)3Cl/Organic Molten Salt[J]. Acta Chimica Sinica, 2008, 66(9): 1009-1014.
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