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[Rh((R)-8-(3,5-dioxa-4-phospha-cyclohepta-[2,1-a;3,4-a']dinaphtalen-4-yl)-quinoline)(acetylacetonate)] | 499199-41-6

中文名称
——
中文别名
——
英文名称
[Rh((R)-8-(3,5-dioxa-4-phospha-cyclohepta-[2,1-a;3,4-a']dinaphtalen-4-yl)-quinoline)(acetylacetonate)]
英文别名
——
[Rh((R)-8-(3,5-dioxa-4-phospha-cyclohepta-[2,1-a;3,4-a']dinaphtalen-4-yl)-quinoline)(acetylacetonate)]化学式
CAS
499199-41-6
化学式
C34H25NO4PRh
mdl
——
分子量
645.456
InChiKey
QABONHANHNQOPU-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

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

反应信息

  • 作为产物:
    参考文献:
    名称:
    Synthesis of Phosphonito,N and Phosphito,N ligands based on quinolines and (R)-binaphthol or substituted biphenol and of their rhodium(I), palladium(II) and platinum(II) complexes
    摘要:
    The new Phosphonito,N ligands 8-(4,8-di-tert-butyl-1,11-dimethoxy-5,7-dioxa-6-phospha-dibenzo[a,c]cyclohepten-6-yl)-quinoline (2a), and (R)-8-(3,5-dioxa-4-phospha-cyclohepta-[2,1-a;3,4-a']dinaphthalen-4-yl)-quinoline ((R)-2b), were readily prepared starting from 8-(bis-diethylamino-phosphine)-quinoline (1), as a key intermediate, and 2,2'-dihydroxy-5,5'-dimethoxy-3,3-di-tert-butylbiphenyl or (R)-binaphthol, respectively. The Phosphito,N ligand, 8-(4,8-di-tert-butyl-1,11-dimethoxy-5,7-dioxa-6-phosphadibenzo[a,c]cyclohepten-6-yloxy)-quinoline (3a), was obtained by reacting equimolar amounts of 8-hydroxyquinoline and the phosphorochloridite derived from 3,3'-di-tert-butyl-2,2'-dihydroxy-5,5'-dimethoxybiphenyl, in toluene in the presence of NEt3. The corresponding Phosphito,N-ligand, 8-(3,5-dioxa-4-phospha-cyclohepta[2,1-a;3,4-a']dinaphthalen-4-yloxy)-quinoline (R)-(3b), was obtained similarly using the phosphorochloridite derived from (R)-binaphthol. A systematic study of the coordination abilities of 2-3 to rhodium(l), palladium(II) and platinum(II) precursors has been carried out. Crystal structures of the complexes [Pt(3a)I-2] (7a), and [Pd(2a)Cl-2] (8a), are reported. The reactions of the chiral ligands (R)-2b and (R)-3b with [Rh(acaC)(CO)(2)] lead to [Rh(acac)(R-2b)] (10), and [Rh(acac)(R-3b)] (11), respectively. Under hydroformylation conditions, displacement of the chiral ligands in both complexes 10 and 11 takes place, even in the presence of an excess of free ligand, leading to achiral hydrido-carbonyl rhodium complexes. (C) 2002 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0020-1693(02)00849-6
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