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cis-trans-[(tetrafluorobenzobarrelene)Ir(H)2(triisopropylphosphine)2](BF4) | 200563-16-2

中文名称
——
中文别名
——
英文名称
cis-trans-[(tetrafluorobenzobarrelene)Ir(H)2(triisopropylphosphine)2](BF4)
英文别名
——
cis-trans-[(tetrafluorobenzobarrelene)Ir(H)2(triisopropylphosphine)2](BF4)化学式
CAS
200563-16-2
化学式
BF4*C30H50F4IrP2
mdl
——
分子量
827.693
InChiKey
YLYBAMOTXRTDDI-MITSAKNPSA-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

  • 作为反应物:
    参考文献:
    名称:
    Synthesis, X-ray Structure, and Catalytic Activity of the Unusual Complex [Ir(TFB)(PiPr3)2]BF4 (TFB = Tetrafluorobenzobarrelene)
    摘要:
    Complex IrCl(TFB)(PiPr(3)) (1) reacts with AgBF4 in the presence of triisopropylphosphine to afford [Ir(TFB)(PiPr(3))(2)]BF4 (2). The structure of 2 was determined by an X-ray diffraction study. The coordination geometry around the iridium center is distorted square-planar with a P-Ir-P angle of 102.7(1)degrees. Complex 2 reacts with molecular hydrogen to give cis-trans-[IrH2(TFB)(PiPr(3))(2)]BF4 (3), and with phenylacetylene to afford Ir(C2Ph)(TFB)(PiPr(3)) (4). Complex 2 is found to be a very active catalyst for the hydrogenation, of olefins and phenylacetylene. In dichloromethane as solvent at 25 degrees C and atmospheric pressure, selectivities close to 80% are achieved for the hydrogenation of the alkyne to alkene.
    DOI:
    10.1021/om970688x
  • 作为产物:
    描述:
    [(tetrafluorobenzobarrelene)Ir(triisopropylphosphine)2](BF4)氢气二氯甲烷 为溶剂, 以87%的产率得到cis-trans-[(tetrafluorobenzobarrelene)Ir(H)2(triisopropylphosphine)2](BF4)
    参考文献:
    名称:
    Synthesis, X-ray Structure, and Catalytic Activity of the Unusual Complex [Ir(TFB)(PiPr3)2]BF4 (TFB = Tetrafluorobenzobarrelene)
    摘要:
    Complex IrCl(TFB)(PiPr(3)) (1) reacts with AgBF4 in the presence of triisopropylphosphine to afford [Ir(TFB)(PiPr(3))(2)]BF4 (2). The structure of 2 was determined by an X-ray diffraction study. The coordination geometry around the iridium center is distorted square-planar with a P-Ir-P angle of 102.7(1)degrees. Complex 2 reacts with molecular hydrogen to give cis-trans-[IrH2(TFB)(PiPr(3))(2)]BF4 (3), and with phenylacetylene to afford Ir(C2Ph)(TFB)(PiPr(3)) (4). Complex 2 is found to be a very active catalyst for the hydrogenation, of olefins and phenylacetylene. In dichloromethane as solvent at 25 degrees C and atmospheric pressure, selectivities close to 80% are achieved for the hydrogenation of the alkyne to alkene.
    DOI:
    10.1021/om970688x
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