陈新兰,扬夕琰.MXn和TPPTS.Ln体系催化1—已烯氢甲酰化反应的新探索[J].分子催化,2001,(6):423-426
MXn和TPPTS.Ln体系催化1—已烯氢甲酰化反应的新探索
A New Approach to Catalyzed Hydroformylation of 1-Heptene with MXn-TPPTS.Ln System
  
DOI:
中文关键词:  氢甲酰化 1-已烯 稀土离子 水溶性膦配体 催化反应 配合物 铑 选择性
英文关键词:
基金项目:This work was supported by the State Key Lab. OSSO (OxoSynthesis and Selective Oxidation) of Lanzhou Institute of Chemical Physics,中国科学院资助项目,,,,
陈新兰  扬夕琰
[1]武汉大学化学系,湖北武汉430072 [2]中国科学院兰州化学物理研究所羰基合成与选择氧化国家重点实验室,甘肃兰州
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中文摘要:
      在可比条件下,研究了新型水溶性膦配体TOPPTS。Ln(TPPTS=三(间碘酸基苯基)膦,Ln=Y,La,Nd,Ho,Yb)分别与RhCl3、NiCl2、PbCl2组成的体系催化1-已烯氢甲酰化反应。结果表明,TPPTS。Ln-RhCl3(Ln-Y、Ho)的催化活性优于TPPTS。Na3-RhCl3体系(1-已烯的转化率分别为49.9%、38.8%、24.3%),有意义的是,TPPTS。Yb-NiCl2体系(转化率44.5%)亦高于TPPTS。Na3-RhCl3体系的催化结果,且稀土离子介入溶性膦配体后,使催化剂支支链醛的选择性明显提高。
英文摘要:
      Some new water-soluble phosphine ligands TPPTS.Ln (TPPTS=tris-(m-sulfonatophenyl)-phosphine,Ln=Y,La,Nd,Ho,Yb) with RhCl3,NiCl2,PdCl2 were used as the catalysts in the hterogeneous (water-organic phase) hydroformylation of 1-hetene,respectively.TPPTS.Ln-RhCl2(Ln=Y,Ho) yield exceptionally high conversion of heptene as compared with RhCl3-TPPTS.Na3 under the conditions used.Using NiCl2-TPPTS.Yb satisfatory conversion of heptene is also obtained and it is much cheaper than RhCl3,so it has great potentiality in the future nidustry process.
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