1,2-W2(i-Bu)2(O-i-Pr)4 | 101860-15-5

• 分子结构分类: 有机化合物 - 有机盐 - 有机金属盐
• 英文名称: 1,2-W2(i-Bu)2(O-i-Pr)4
• CAS: 101860-15-5
• 化学式: C₂₀H₄₆O₄W₂
• 分子量: 718.283
• InChiKey: NJLCRTAWDZIIIV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.72
• 重原子数：
  26.0
• 可旋转键数：
  13.0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  36.92
• 氢给体数：
  0.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  1,2-W2(i-Bu)2(O-i-Pr)4 在 H₂ 作用下， 以 not given 为溶剂， 以40%的产率得到
  参考文献：
  名称：

  Chisholm. Malcolm H.; Kramer, Keith S.; Streib, William E., Journal of the American Chemical Society, 1992, vol. 114, p. 3571 - 3573

  摘要：

  DOI：
• 作为产物：
  描述：

  W2(i-Bu)2(NMe2)4 、 异丙醇 以 正己烷 为溶剂， 生成 1,2-W2(i-Bu)2(O-i-Pr)4
  参考文献：
  名称：

  Chisholm, Malcolm H.; Eichhorn, Bryan W.; Folting, Kirsten, Organometallics, 1986, vol. 5, # 8, p. 1599 - 1606

  摘要：

  DOI：

文献信息

• Polynuclear Metal Hydrido Alkoxides. 2. Hydrogenation of 1,2-W₂(ⁱBu)₂(OⁱPr)₄. Preparation, Characterization, and Some Reactions of W₆H₅(CⁱPr)(OⁱPr)₁₂, W₂(H)₂(OⁱPr)₄(dmpe)₂, and W₄(H)₄(dmpm)₃, Where dmpe = Bis(dimethylphosphino)ethane and dmpm = Bis(dimethylphosphino)methane
  作者：Malcolm H. Chisholm、Kirsten Folting、Keith S. Kramer、William E. Streib

  DOI：10.1021/ja9643634

  日期：1997.6.1

  H-2 and 1,2-W-2(Bu-i)(2)((OPr)-Pr-i)(4) react in hydrocarbon solvents to give the cluster W-6(H)(5)((CPr)-Pr-i)((OPr)-Pr-i)(12) (1) in 40% crystalline yield. W-2(H)(2)((OPr)-Pr-i)(4)(dmpe)(2) (2) and W-4(H)(4)((OPr)-Pr-i)(8)(dmpm)(3) (3) have been isolated in the presence of the chelating diphosphines Me2PCH2CH2PMe2 (dmpe) and Me2PCH2PMe2 (dmpm). Reactions involving the use of various isotopes reveal the importance of both alpha- and beta-CH activation of the Bu-i ligand. An X-ray determination and NMR data reveal that 1 contains an octahedral W-6 unit, W-W = 2.58 to 2.85 Angstrom, supported by four bridging hydride ligands, seven bridging alkoxides, and one bridging isobutylidyne ligand in addition to five terminal (OPr)-Pr-i and one terminal hydride: W-6(H)(mu-H)(4)(mu-(CPr)-Pr-i)(mu-(OPr)-Pr-i)(7)((OPr)-Pr-i)(5). Only one isomer is observed crystallographically, and the NMR data are indicative of its presence in solution. The cluster 1 is inert with respect to intramolecular ligand site exchange, which has allowed the detection of preferential hydrogenolysis and hydrogenation involving the terminal W-H ligand while alcoholysis occurs preferentially at the terminal W-(OPr)-Pr-i site adjacent to three mu-H ligands. In the solid state, compound 2 has four terminal (OPr)-Pr-i ligands on one W atom and two dmpe ligands on the other: ((PrO)-Pr-i)(4)W(mu-H)(2)W(dmpe)(2), W-W = 2.49 Angstrom. The locations of the two mu-H ligands are inferred from the X-ray determination and their proposed locations are consistent with the hydride-locating program XHYDEX. In solution, 2 is fluxional and low-temperature H-1 and P-31H-1) NMR spectra are consistent with the presence of two isomers, one of which is the same as that seen in the solid state while the other has the more symmetrical disposition of ligands (dmpe)((PrO)-Pr-i)(2)W(mu-H)(2)W((OPr)-Pr-i)(2)(dmpe). Compound 3 contains a chain of four tungsten atoms with terminal W-W distances of similar to 2.5 Angstrom and a central W to W distance of 3.6 Angstrom, bridged by three dmpm ligands. The solid-state molecular structure is proposed as ((PrO)-Pr-i)(3)W(mu-H)(mu-(OPr)-Pr-i)W(mu-dmpm)(3)(mu-H)W((OPr)-Pr-i)(4). The solution NMR data reveal that 3 is fluxional but that at low temperatures a structure akin to that formulated above is present. These results are discussed in terms of the developing chemistry of hydride alkoxides of the early transition elements.