trans-chloro(methoxycarbonyl)bis(triphenylphosphine)platinum(II) | 22654-30-4

• 英文名称: trans-chloro(methoxycarbonyl)bis(triphenylphosphine)platinum(II)
• 英文别名: trans-(Ph3P)2Pt(CO2CH3)Cl
• CAS: 22654-30-4；20524-02-1
• 化学式: C₃₈H₃₃ClO₂P₂Pt
• 分子量: 814.159
• InChiKey: VUTILVJHNCTYHL-UHFFFAOYSA-M

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：

  trans-chloro(methoxycarbonyl)bis(triphenylphosphine)platinum(II) 以 二氯甲烷 为溶剂， 生成 trans-[(Ph3P)2Pt(CO)(OTf)]OTf
  参考文献：
  名称：

  Synthesis and characterization of bifunctional trans-(Ph3P)2Pt(CO2Me)(X) complexes

  摘要：

  A series of trans-(Ph(3)P)(2)Pt(X)(Y) complexes (X = CO(2)Me or CO; Y = CO(2)Me, CO, OMe, OTf) has been prepared in order to determine the compatibility of electrophilic (CO, CO(2)Me) and nucleophilic (OH, OMe) ligands in the same platinum coordination sphere. Dealkoxylation of CO(2)Me complexes by trimethylsilyl triflate affords the corresponding cationic carbonyl derivatives, and represents a potentially useful metalloester deprotection method for controlling the formation of dimetalloester linkages. The crystal structure of [trans-(Ph(3)P)(2)Pt(CO(2)Me)(CO)]BF4 has been determined, and reveals an unusual distortion of the P-Pt-P angle perpendicular to the square planar coordination geometry. Attempted condensation reactions between trans-(Ph(3)P)(2)Pt(CO(2)Me)(CO)(+) and trans-(Ph(3)P)(2)Pt(CO(2)Me)(OH) did not yield a dimetalloester condensation product, presumably due to the steric bulk of the ancillary Ph(3)P ligands.

  DOI：

  10.1016/0022-328x(94)05076-n
• 作为产物：
  描述：

  trans-(Ph3P)2Pt(CO2CH3)(OCH3) 在 chlorinated solvents 作用下， 以 四氢呋喃 为溶剂， 生成 trans-chloro(methoxycarbonyl)bis(triphenylphosphine)platinum(II)
  参考文献：
  名称：

  Synthesis and characterization of bifunctional trans-(Ph3P)2Pt(CO2Me)(X) complexes

  摘要：

  A series of trans-(Ph(3)P)(2)Pt(X)(Y) complexes (X = CO(2)Me or CO; Y = CO(2)Me, CO, OMe, OTf) has been prepared in order to determine the compatibility of electrophilic (CO, CO(2)Me) and nucleophilic (OH, OMe) ligands in the same platinum coordination sphere. Dealkoxylation of CO(2)Me complexes by trimethylsilyl triflate affords the corresponding cationic carbonyl derivatives, and represents a potentially useful metalloester deprotection method for controlling the formation of dimetalloester linkages. The crystal structure of [trans-(Ph(3)P)(2)Pt(CO(2)Me)(CO)]BF4 has been determined, and reveals an unusual distortion of the P-Pt-P angle perpendicular to the square planar coordination geometry. Attempted condensation reactions between trans-(Ph(3)P)(2)Pt(CO(2)Me)(CO)(+) and trans-(Ph(3)P)(2)Pt(CO(2)Me)(OH) did not yield a dimetalloester condensation product, presumably due to the steric bulk of the ancillary Ph(3)P ligands.

  DOI：

  10.1016/0022-328x(94)05076-n

文献信息

• Photochemistry of some alkoxycarbonylplatinum(II) complexes
  作者：Conrad F. Shiba、Walter H. Waddell

  DOI：10.1016/0022-328x(83)80031-x

  日期：1983.1