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[Ru(η6-4-phenyl-2-butanol)(1,3,5-triaza-7-phosphatricyclo[3.3.1.1]decane)Cl2] | 876728-15-3

中文名称
——
中文别名
——
英文名称
[Ru(η6-4-phenyl-2-butanol)(1,3,5-triaza-7-phosphatricyclo[3.3.1.1]decane)Cl2]
英文别名
——
[Ru(η6-4-phenyl-2-butanol)(1,3,5-triaza-7-phosphatricyclo[3.3.1.1]decane)Cl2]化学式
CAS
876728-15-3
化学式
C16H26Cl2N3OPRu
mdl
——
分子量
479.352
InChiKey
JVWPKWMCGTZTTA-RASHCQHBSA-L
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

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:
    氟硼酸铵[Ru(η6-4-phenyl-2-butanol)(1,3,5-triaza-7-phosphatricyclo[3.3.1.1]decane)Cl2]三苯基膦甲醇 为溶剂, 以91%的产率得到[Ru(η6-4-phenyl-2-butanol)(1,3,5-triaza-7-phosphatricyclo[3.3.1.1]decane)Cl(triphenylphosphine)]BF4
    参考文献:
    名称:
    Use of Perfluorinated Phosphines to Provide Thermomorphic Anticancer Complexes for Heat-Based Tumor Targeting
    摘要:
    A series of compounds of general formula [Ru(eta(6)-arene)(pta)(PR3)Cl]BF4 (arene = p-cymene or 4-phenyl-2-butanol; pta = 1,3,5-triaza-7-phosphatricyclo[3.3.1.1]decane, PR3 = PPh2(p-C6H4C2H4C8F17), PPh(p-C6H4C2H4C8F17)(2), P(p-C6H4C2H4C6F13)(3), PPh3 or P(p-C6H4F)(3)) have been prepared and characterized by spectroscopic methods. The structure of [Ru(eta(6)-p-cymene)(pta)Cl(P(p-C6H4F)(3))]BF4 has also been established in the solid state by X-ray crystallography. The cytotoxicities of the compounds were determined in the A2780 and A2780 cisplatin-resistant cell lines revealing that the fluorinated phosphines significantly increase antiproliferative activity relative to their bis-chloride precursors. Two of the complexes were found to be thermoresponsive, that is, showing poor water solubility at 37 degrees C and good solubility at 42 degrees C, the temperature of a heated tumor, providing a method of tumor targeting. Incubation at 42 degrees C for 2 h resulted in improved cytotoxicities for two of the complexes.
    DOI:
    10.1021/ic9020433
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