(1,5-cyclooctadiene)Pt(C6H4-4-Cl)Cl | 57110-59-5

• 英文名称: (1,5-cyclooctadiene)Pt(C6H4-4-Cl)Cl
• 英文别名: Pt(cyclo-octa-1,5-diene)(C6H4Cl-p)Cl
• CAS: 57110-59-5
• 化学式: C₁₄H₁₆Cl₂Pt
• 分子量: 450.267
• InChiKey: GHYQPTBDQFGDHO-PHFPKPIQSA-M

计算性质

• 辛醇/水分配系数(LogP)：
  None
• 重原子数：
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• 可旋转键数：
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• 环数：
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• sp3杂化的碳原子比例：
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• 拓扑面积：
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• 氢给体数：
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• 氢受体数：
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反应信息

• 作为反应物：
  描述：

  (1,5-cyclooctadiene)Pt(C6H4-4-Cl)Cl 在 1,2-双(二苯基膦)乙烷 作用下， 以 二氯甲烷 为溶剂， 生成 Pt(C₆H₄Cl-p)Cl(1,2-bis(diphenylphosphino)ethane)
  参考文献：
  名称：

  Eaborn, Colin; Odell, Kevin J.; Pidcock, Alan, Journal of the Chemical Society, Dalton Transactions

  摘要：

  DOI：
• 作为产物：
  描述：

  (4-氯苯基)-三甲基锡烷 、 dichloro( 1,5-cyclooctadiene)platinum(ll) 以 further solvent(s) 为溶剂， 以73%的产率得到(1,5-cyclooctadiene)Pt(C6H4-4-Cl)Cl
  参考文献：
  名称：

  Eaborn, Colin; Odell, Kevin J.; Pidcock, Alan, Journal of the Chemical Society, Dalton Transactions

  摘要：

  DOI：

文献信息

• Distinct Electronic Effects on Reductive Eliminations of Symmetrical and Unsymmetrical Bis-Aryl Platinum Complexes
  作者：Shashank Shekhar、John F. Hartwig

  DOI：10.1021/ja0480365

  日期：2004.10.1

  Symmetrical bis-aryl platinum complexes (DPPF)Pt(C6H4-4-R)(2) (R = NMe2, OMe, CH3, H, Cl, CF3) and electronically unsymmetrical bis-aryl platinum complexes (DPPF)Pt(C6H4-4-R) (C6H4-4-X) (R = CH3, X = NMe2, OMe, H, Cl, F, CF3; R = OMe, X = NMe2, H, Cl, F, CF3; R = CF3, X = H, Cl, NMe2; and R = NMe2, X = H, Cl) were prepared, and the rates of reductive elimination of these complexes in the presence of excess PPh3 are reported. The platinum complexes reductively eliminated biaryl compounds in quantitative yields with first-order rate constants that were independent of the concentration of PPh3. Plots of Log(k(obs)/k(obs(H))) vs Hammett substituent constants (sigma) of the para substituents R and X showed that the rates of reductive elimination reactions depended on two different electronic properties. The reductive elimination from symmetrical bis-aryl platinum complexes occurred faster from complexes with more electron-donating para substituents R. However, reductive elimination from a series of electronically unsymmetrical bis-aryl complexes was not faster from complexes with the more electron-donating substituents. Instead, reductive elimination was faster from complexes with a larger difference in the electronic properties of the substituents on the two platinum-bound aryl groups. The two electronic effects can complement or cancel each other. Thus, this combination of electronic effects gives rise to complex, but now more interpretable, free energy relationships for reductive elimination.