(+/-)-[(1-dibenzophospholylmethyl-1-di(3,5-dimethylphenyl)phosphinylmethyl-1-diphenylphosphinyl-methylethane)(η(4)-1,5-cyclooctadiene)rhodium(I)] hexafluorophosphate | 192824-97-8

• 英文名称: (+/-)-[(1-dibenzophospholylmethyl-1-di(3,5-dimethylphenyl)phosphinylmethyl-1-diphenylphosphinyl-methylethane)(η(4)-1,5-cyclooctadiene)rhodium(I)] hexafluorophosphate
• CAS: 192824-97-8
• 化学式: C₅₃H₅₇P₃Rh*F₆P
• 分子量: 1034.83
• InChiKey: PAHIWQCBHQKITE-APLQMSBUSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  None
• 重原子数：
  None
• 可旋转键数：
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• 环数：
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• sp3杂化的碳原子比例：
  None
• 拓扑面积：
  None
• 氢给体数：
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• 氢受体数：
  None

反应信息

• 作为产物：
  描述：

  六氟磷酸钾 、 di-μ-chloro-bis(1,5-cyclooctadiene)dirhodium 、 (+/-)-(1-dibenzophospholylmethyl-1-di(3,5-dimethylphenyl)phosphinylmethyl)-1-diphenylphosphinyl-methylethane 以 二氯甲烷 、 丙酮 为溶剂， 以99%的产率得到(+/-)-[(1-dibenzophospholylmethyl-1-di(3,5-dimethylphenyl)phosphinylmethyl-1-diphenylphosphinyl-methylethane)(η(4)-1,5-cyclooctadiene)rhodium(I)] hexafluorophosphate
  参考文献：
  名称：

  Rhodium—COD-Komplexe chiraler Tripod-Liganden mit drei verschiedenen Donorgruppen: Komplexchemie und Katalyse

  摘要：

  The reaction of the chiral tripod ligands X2POCH(CH2P(Ph)(2))(CH2PR2) ((+/-)- and R-1a,b: X-2 = 2,2'-biphenoxy-; PR2 = P(4-Me-C6H4)(2) (1a), PR2 = dibenzophospholyl(DBP)- (1b)) and MeC(CH2P(Ph)(2))(CH2PR'(2))(CH2PR''(2)) ((+/-)- and R-2: PR'(2) = P(3,5-Me-2-C6H3)(2); PR'(2); = DBP) with [Rh-I(COD)Cl](2) is investigated. It yields tripod rhodium COD complexes [(1a,b)Rh-I(COD)]PF6 ((+/-)- and R-3a,b) and [(2)Rh-I(COD)]PF6 ((+/-)- and R-4). The tripod ligand is coordinated by all three donor groups in each case, irrespective of the different donor capabilities of the coordinating groups.The complexes 3a,b and 4 are catalysts for the hydrogenation of the prochiral olefins acetamidocinnamic acid and dimethylitaconate. Both the poor activity and the low enantioselectivity compared to rhodium complexes containing chiral bisphosphino ligands can be explained by the presence of a third coordinating donor group in the ligand. Thus the trihapto coordination of the tripodal ligands is shown to be more of an impediment for this type of catalytic transformation.

  DOI：

  10.1016/s0022-328x(96)06930-6