| 428863-80-3

• CAS: 428863-80-3
• 化学式: C₂₆H₄₉P₂Pd
• 分子量: 531.032
• InChiKey: ATLXWPNNTOFFHX-JAHQOBLHSA-N

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：
  描述：

  四氢呋喃 、 、 、 C13取代的一氧化碳 以 四氢呋喃 、 氘代四氢呋喃 为溶剂， 生成 、
  参考文献：
  名称：

  Characterization and Dynamics of [Pd(L−L)H(solv)]⁺, [Pd(L−L)(CH₂CH₃)]⁺, and [Pd(L−L)(C(O)Et)(THF)]⁺ (L−L = 1,2-(CH₂PBu^t₂)₂C₆H₄):  Key Intermediates in the Catalytic Methoxycarbonylation of Ethene to Methylpropanoate

  摘要：

  A detailed spectroscopic study has allowed the solution structure and dynamic properties of all the intermediates in the Pd-catalyzed methoxycarbonylation of ethene to be established. [Pd(L-L)H(solv)](-) 1 (L-L = 1,2-(CH2PBu2t)(2)C6H4; solv = MeOH, 1a; (PrOH)-O-n, 1b; THF, 1c; EtCN, 1d) is static, and the two inequivalent P atoms do not become equivalent through solvent exchange over all the temperatures studied. [Pd(L-L)(CH2CH3)](+), 2, contains a strong beta-agostic C-H interaction which is remarkably stable and is not displaced even in strongly coordinating solvents such as EtCN. C-alpha and C-beta Of the ethyl group in 2 become equivalent via a stereospecific interchange involving [Pd(L-L)H(eta(2)-C2H4)](+) without making the two P atoms equivalent; at higher temperatures these two inequivalent P atoms do become equivalent probably via a T-shaped intermediate. For [Pd(L-L)(C(O)Et)(solv)](+), 6, there is no beta-agostic C-H interaction and multiple C-13-labeling of the C(O)Et group shows that the inequivalent P atoms become equivalent via movement of the intact C(O)Et group. The crystal structure of the related complex [Pd(L-L)(C(O)Et)Cl] cocrystallized with dibenzylacetone has been determined.

  DOI：

  10.1021/om010938g
• 作为产物：
  描述：

  以 甲醇 、 氘代甲醇 为溶剂， 生成 、
  参考文献：
  名称：

  Characterization and Dynamics of [Pd(L−L)H(solv)]⁺, [Pd(L−L)(CH₂CH₃)]⁺, and [Pd(L−L)(C(O)Et)(THF)]⁺ (L−L = 1,2-(CH₂PBu^t₂)₂C₆H₄):  Key Intermediates in the Catalytic Methoxycarbonylation of Ethene to Methylpropanoate

  摘要：

  A detailed spectroscopic study has allowed the solution structure and dynamic properties of all the intermediates in the Pd-catalyzed methoxycarbonylation of ethene to be established. [Pd(L-L)H(solv)](-) 1 (L-L = 1,2-(CH2PBu2t)(2)C6H4; solv = MeOH, 1a; (PrOH)-O-n, 1b; THF, 1c; EtCN, 1d) is static, and the two inequivalent P atoms do not become equivalent through solvent exchange over all the temperatures studied. [Pd(L-L)(CH2CH3)](+), 2, contains a strong beta-agostic C-H interaction which is remarkably stable and is not displaced even in strongly coordinating solvents such as EtCN. C-alpha and C-beta Of the ethyl group in 2 become equivalent via a stereospecific interchange involving [Pd(L-L)H(eta(2)-C2H4)](+) without making the two P atoms equivalent; at higher temperatures these two inequivalent P atoms do become equivalent probably via a T-shaped intermediate. For [Pd(L-L)(C(O)Et)(solv)](+), 6, there is no beta-agostic C-H interaction and multiple C-13-labeling of the C(O)Et group shows that the inequivalent P atoms become equivalent via movement of the intact C(O)Et group. The crystal structure of the related complex [Pd(L-L)(C(O)Et)Cl] cocrystallized with dibenzylacetone has been determined.

  DOI：

  10.1021/om010938g