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作 者:郑宏杰[1] 李敏[1] 陈华[1] 李瑞祥[1] 李贤均[1]
机构地区:[1]四川大学化学学院有机金属络合催化研究所,绿色化学与技术教育部重点实验室,四川成都610064
出 处:《催化学报》2005年第1期4-6,共3页
基 金:国家重点基础研究发展规划资助项目 (G2 0 0 0 0 480 0 8)
摘 要:The hydroformylation of 1-hexene catalyzed by rhodium-TPPTS complexes in the ionic liquid [bmim]BF 4 was studied. The activity and selectivity of the rhodium-TPPTS complexes in [bmim]BF 4 were much higher than those reported in other ionic liquids. The TOF of 1-hexene and selectivity for aldehyde were 1508 h -1 and 92%, respectively, under the optimum conditions. The high activity of the catalyst is ascribed to the absence of halide ions as well as the much higher solubility of hydrogen and rhodium-TPPTS complexes in [bmim]BF 4 than in [bmim]PF 6.The hydroformylation of 1-hexene catalyzed by rhodium-TPPTS complexes in the ionic liquid [bmim]BF4 was studied. The activity and selectivity of the rhodium-TPPTS complexes in [bmim]BF4 were much higher than those reported in other ionic liquids. The TOF of 1-hexene and selectivity for aldehyde were 1 508 h(-1) and 92 % , respectively, under the optimum conditions. The high activity of the catalyst is ascribed to the absence of halide ions as well as the much higher solubility of hydrogen and rhodium-TPPTS complexes in [bmim]BF4 than in [bmim]PF6.
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