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首页> 外文期刊>New Journal of Chemistry >High pressure infrared and nuclear magnetic resonance studies of the rhodium-sulfoxantphos catalysed hydroformylation of 1-octene in ionicliquids
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High pressure infrared and nuclear magnetic resonance studies of the rhodium-sulfoxantphos catalysed hydroformylation of 1-octene in ionicliquids

机译:铑-亚砜基磷光催化离子液体中1-辛烯加氢甲酰化的高压红外和核磁共振研究

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The rhodium-sulfoxantphos catalysed hydroformylation of 1-octene in 1-n-butyl-3-methylimidazolium hexafluorophosphate(BMI.PF_6)as a room temperature ionic liquid was monitored in situ by high pressure IR(HP-IR)and NMR(HP-NMR).Similar ee(bis-equatorial)and ea(equatorial-apical)(diphosphine)Rh(CO)_2H catalytic species,as observed in organic solvents,are formed in the BMI.PF_6 ionicliuid.The ratio of the ee and ea isomers is influenced by both the temperature and syngas pressure.An increase in hydrogen partial pressure has no effect on the activity of the system during the reaction performed in BMI:PF_6,while some hydrogormylation systems using xanthene backbone ligands in conventional organic solvents can be sensitive to hydrogen partial pressure.
机译:通过高压IR(HP-IR)和NMR(HP-IR)原位监测铑-硫氧黄磷催化的1-辛烯在1-正丁基-3-甲基咪唑六氟磷酸盐(BMI.PF_6)中作为室温离子液体的加氢甲酰化反应在有机溶剂中观察到,在BMI中形成了类似的ee(双-赤道)和ea(赤道-顶)(二膦)Rh(CO)_2H催化物种.PF_6离子液体.ee和ea的比率异构体受温度和合成气压力的影响。在BMI:PF_6中进行反应期间,氢分压的升高对系统的活性没有影响,而某些在常规有机溶剂中使用x吨骨架配体的加氢缩醛化系统可能很敏感。氢分压。

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