[RuCl(tris(2-dicyclohexylphosphinoethyl)phosphine)]Cl | 146816-53-7

• 分子结构分类: 有机化合物 - 有机磷化合物
• 英文名称: [RuCl(tris(2-dicyclohexylphosphinoethyl)phosphine)]Cl
• CAS: 146816-53-7
• 化学式: C₄₂H₇₈ClP₄Ru*Cl
• 分子量: 878.952
• InChiKey: YRCCESJHVXOORI-UHFFFAOYSA-L

计算性质

• 辛醇/水分配系数(LogP)：
  12.6
• 重原子数：
  49.0
• 可旋转键数：
  6.0
• 环数：
  9.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  0.0
• 氢给体数：
  0.0
• 氢受体数：
  0.0

反应信息

• 作为反应物：
  描述：

  [RuCl(tris(2-dicyclohexylphosphinoethyl)phosphine)]Cl 在 NaOCH₃ 作用下， 以 四氢呋喃 为溶剂， 以85%的产率得到
  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
• 作为产物：
  描述：

  tris(triphenylphosphine)ruthenium(II) chloride 、 tris(2-(dicyclohexylphosphanyl)ethyl)phosphane 以 二氯甲烷 为溶剂， 以88%的产率得到[RuCl(tris(2-dicyclohexylphosphinoethyl)phosphine)]Cl
  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

文献信息

• Low Oxidation State Iron(0), Iron(I), and Ruthenium(0) Dinitrogen Complexes with a Very Bulky Neutral Phosphine Ligand
  作者：Ryan Gilbert-Wilson、Leslie D. Field、Stephen B. Colbran、Mohan M. Bhadbhade

  DOI：10.1021/ic3024953

  日期：2013.3.18

  cationic dinitrogen species [Fe(N2)H(P2P3Cy)]+ (6) and [Ru(N2)H(P2P3Cy)]+ (7) were formed by treatment of 1 and 3, respectively, with 1 equiv of a weak organic acid. The iron(II) complex Fe(H)2(P2P3Cy) (5) was also synthesized and characterized. Complexes [RuCl(P2P3Cy)][BPh4], 1, 2, 3[BPh4], 4, 5, 6[BF4], and 7[BF4] were characterized by X-ray crystallography. The Fe(I) and Ru(I) complexes 3 and 4 were

  描述了一系列具有配体P 2 P 3 Cy，P（CH 2 CH 2 PCy 2）3的铁和钌配合物的合成。铁（0）和钌（0）配合物Fe（N 2）（P 2 P 3 Cy）（1）和Ru（N 2）（P 2 P 3 Cy）（2）通过[FeCl（ P 2 P 3 Cy）] +和[RuCl（P 2 P 3 Cy）] +在氮气氛下用过量的钾石墨。通过[FeCl（P）的处理合成了Fe（I）和Ru（I）物种[Fe（N 2）（P 2 P 3 Cy）] +（3）和RuCl（P 2 P 3 Cy）（4）。2 P 3 Cy）] +和[RuCl（P 2 P 3 Cy）] +和1当量的钾石墨在氮气氛下。阳离子二氮物种[Fe（N 2）H（P 2 P 3 Cy）] +通过分别用1当量的弱有机酸处理1和3，形成（6）和[Ru（N 2）H（P 2 P 3 Cy）] +（7）。还合成并表征了铁（II）配合物Fe（H）2（P 2 P 3