dihydrido(η(2)-2,6-pyridinedicarboxaldehyde 2-hydroxyethylimine-N,N')bis(triphenylphosphine)iridium(III) tetrafluoroborate | 175698-75-6

• 英文名称: dihydrido(η(2)-2,6-pyridinedicarboxaldehyde 2-hydroxyethylimine-N,N')bis(triphenylphosphine)iridium(III) tetrafluoroborate
• CAS: 175698-75-6
• 化学式: BF₄*C₄₅H₄₂IrN₂O₂P₂
• 分子量: 983.813
• InChiKey: ZIJYLNVRTAPMAW-BGEJTCBGSA-N

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：
  None
• 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：

  dihydrido(η(2)-2,6-pyridinedicarboxaldehyde 2-hydroxyethylimine-N,N')bis(triphenylphosphine)iridium(III) tetrafluoroborate 、 C.I.酸性橙108 以 苯 为溶剂， 以68%的产率得到dihydrido(η(2)-2,6-pyridinedicarboxaldehyde bis(2-hydroxyethylimine)-N,N')bis(triphenylphosphine)iridium(III) tetrafluoroborate
  参考文献：
  名称：

  An η¹-Aldehyde Complex and the Role of Hydrogen Bonding in Its Conversion to an η¹-Imine Complex

  摘要：

  2-Pyridinecarboxaldehyde displaces Me(2)CO from [IrHz(Me(2)CO)(2)(PPh(3))(2)](+) to give a chelating N,O-bound product containing an eta(1)-O-bound aldehyde group. This is converted to the eta(1)-N-bound imine complex with a variety of substituted amines. When the amine contains a suitably positioned -OH group, intramolecular O-H ... H-Ir dihydrogen bonds are detected in the products. This hydrogen bonding influences the relative rates of product formation from 2- and 4-aminophenol (rate ratio 6:1), where only the 2-isomer is capable of forming an intramolecular H-bond.

  DOI：

  10.1021/ic9508076
• 作为产物：
  描述：

  dihydrido(η(2)-2,6-pyridinedicarboxaldehyde-N,O)bis(triphenylphosphine)iridium(III) tetrafluoroborate 、 C.I.酸性橙108 以 苯 为溶剂， 以93%的产率得到dihydrido(η(2)-2,6-pyridinedicarboxaldehyde 2-hydroxyethylimine-N,N')bis(triphenylphosphine)iridium(III) tetrafluoroborate
  参考文献：
  名称：

  An η¹-Aldehyde Complex and the Role of Hydrogen Bonding in Its Conversion to an η¹-Imine Complex

  摘要：

  2-Pyridinecarboxaldehyde displaces Me(2)CO from [IrHz(Me(2)CO)(2)(PPh(3))(2)](+) to give a chelating N,O-bound product containing an eta(1)-O-bound aldehyde group. This is converted to the eta(1)-N-bound imine complex with a variety of substituted amines. When the amine contains a suitably positioned -OH group, intramolecular O-H ... H-Ir dihydrogen bonds are detected in the products. This hydrogen bonding influences the relative rates of product formation from 2- and 4-aminophenol (rate ratio 6:1), where only the 2-isomer is capable of forming an intramolecular H-bond.

  DOI：

  10.1021/ic9508076