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| 146816-62-8

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
146816-62-8
化学式
C24H20B*C42H81FeP4
mdl
——
分子量
1085.08
InChiKey
RBSCWDMMUOAUJD-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:
    四苯硼钠 、 lithium aluminium tetrahydride 以 四氢呋喃 为溶剂, 生成
    参考文献:
    名称:
    Use of the new ligand P(CH2CH2PCy2)3 in the synthesis of dihydrogen complexes of iron(II) and ruthenium(II)
    摘要:
    The novel bulky and basic tetradentate ligand P(CH2CH2PCy2)3 (PP3Cy) is synthesized by the LiN(i-Pr)2-Catalyzed addition reaction of dicyclohexylphosphine (HPCy2) to P(CH=CH2)3. Treatment of RuCl2(PPh3)3 with PP3Cy produces the five-coordinate square-pyramidal complex [RuCl(PP3CY)]Cl, Which is converted into [RuCl(PP3Cy)]BPh4 when treated with NaBPh4. Similarly, FeCl2 reacts with PP3CY to give [FeCl(PP3CY)]Cl. The structure of the tetraphenylborate salt [FeCI(PP3CY)] BPh4 is trigonal bipyramidal around Fe(II); crystals are monoclinic, space group P2(1)/c, with a = 12.699(4) angstrom, b = 29.046(16) angstrom, c = 17.026(7) angstrom, beta = 103.14(3)-degrees, and V = 6116(5) angstrom3 for Z = 4; R = 0.065. Reaction of [RuCl(PP3Cy)]Cl with excess NaBH4 in THF yields mer-RuH(eta2-BH4)(eta3-PP3Cy.BH3), where the tetraphosphine is bound via three P atoms to ruthenium and the BH3 is bound to a dangling terminal PCY2 group of the tetraphosphine. The monohydride complex RuHCl(PP3Cy) is obtained from the reaction of [RuCl(PP3CY)]Cl with excess NaOMe in refluxing THF. The eta2-dihydrogen complex[RuH(eta2-H2)(PP3CY)]BPh4 is synthesized by treating [RuCl(PP3CY)]BPh4 with 1 equiv of NaBH4 under an atmosphere of dihydrogen. The analogous iron complex is also described. The nonclassical structures of [MH(eta2-H2)(PP3CY)]BPh4 (M = Fe, Ru) are established by H-1, P-31, and T1 NMR measurements and the observation of a 1J(HD) coupling constant of 28 Hz in the isotopomer [RuD(HD)(PP3-Cy)]+. Despite the steric bulk of the ligand, the complexes adopt an octahedral geometry, [MH(H2)(PP3CY)]+, instead of a trigonal-bipyramidal ligand geometry with an H3 ligand.
    DOI:
    10.1021/om00027a046
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