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trans-mesitylacetonitrilebis(tricyclohexylphosphine)nickel(II) tetrafluoroborate | 205449-56-5

中文名称
——
中文别名
——
英文名称
trans-mesitylacetonitrilebis(tricyclohexylphosphine)nickel(II) tetrafluoroborate
英文别名
——
trans-mesitylacetonitrilebis(tricyclohexylphosphine)nickel(II) tetrafluoroborate化学式
CAS
205449-56-5
化学式
BF4*C47H80NNiP2
mdl
——
分子量
866.601
InChiKey
KFLHQKRMEYSVIW-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:
    描述:
    四氟化硼(+3)铊(+1) 、 {NiBr(2,4,6-Me3C6H2)(PCy3)2} 以 四氢呋喃 为溶剂, 以55%的产率得到trans-mesitylacetonitrilebis(tricyclohexylphosphine)nickel(II) tetrafluoroborate
    参考文献:
    名称:
    Hydrovinylation of olefins catalyzed by cationic nickel complexes [Ni(2,4,6-Me3C6H2) (CH3CN) P2]BF4
    摘要:
    The hydrovinylation of several olefins and alkynes by the ionic nickel precursor trans-[Ni(2,4,6-Me3C6H2)(CH3CN)(P(CH2Ph)(3))(2)]BF4 in THF solution was studied. The activity of the catalytic system showed strong dependence on the nature of the substrate. Only conjugated diolefins and some strained mono-olefins led to hydrovinylation products with nearly complete conversion. Selectivity was also variable: for norbornene, exo-2-vinylnorbornane (94%) was obtained selectively, whereas isoprene gave a mixture of 9 hydrovinylation compounds. The turnover rate of the reaction at 25 degrees C and 15 bar of initial pressure of ethylene with an olefin/[Ni] ratio of 1000/1 was 4300 h(-1) for norbornene and 30 h(-1) for isoprene. The chiral monodentate phosphines, (cis-myrtanyl)diphenylphosphine and myrtenyldiphenylphosphine, were obtained. The catalytic precursors containing these phosphines were bring tested in the hydrovinylation of styrene and norbornene, and the enantiomeric excess obtained was between 3-7%. Diphenylacetylene was also found to be active in the hydrovinylation reaction; cis- and trans-3,4-diphenyl-1,3-hexadiene, products of a double vinylation of the triple bond were obtained. (C) 1997 Elsevier Science B.V.
    DOI:
    10.1016/s1381-1169(97)00082-4
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