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| 186912-18-5

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
186912-18-5
化学式
C21H22Cl3O2Rh
mdl
——
分子量
515.669
InChiKey
ITTLEVUDPNJHBU-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

反应信息

  • 作为产物:
    描述:
    在 C5H5Tl 作用下, 以 四氢呋喃 为溶剂, 生成
    参考文献:
    名称:
    An unusual example ofendo-stereoselectivity in the ligand exchange reactions of rhodium(i)diethylene derivatives withpara-semiquinoid ligands
    摘要:
    The ligand exchange reactions of [(C2H4)(2)Rh(acac)] in benzene and [(C2H4)(2)RhCl](2) in CH2Cl2 with 4-methyl-4-trichloromethyl-2,5-cyclohexadiene-1-one occur with 100% exo-stereoselectivity. The similar process with 4-methyl-4-trichloromethyl-1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-2,5-cyclohexadiene (trienedione) is strictly exo-stereospecific only if [(C2H4)(2)Rh(acac)] in benzene is used, while in the case of [(C2H4)(2)RhCl](2) in CH2Cl2, it proceeds with an endo-stereoselectivity of 43%. An explanation for these facts has been suggested that assumes that the metal atom initially attacks the central double bond in the trienedione, which is removed from the area of main steric hindrance. The subsequent metallotropic rearrangement of the resulting ethylene-triene intermediate gives rise to the final eta(4)-coordinated pi-diene structures.
    DOI:
    10.1007/bf01430741
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