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(1,3-bis(4-acetylphenyl)triaz-2-en-1-yl)bis(triphenyl-l5-phosphaneyl)palladium(IV) chloride | 1352513-44-0

中文名称
——
中文别名
——
英文名称
(1,3-bis(4-acetylphenyl)triaz-2-en-1-yl)bis(triphenyl-l5-phosphaneyl)palladium(IV) chloride
英文别名
——
(1,3-bis(4-acetylphenyl)triaz-2-en-1-yl)bis(triphenyl-l5-phosphaneyl)palladium(IV) chloride化学式
CAS
1352513-44-0
化学式
C52H44ClN3O2P2Pd
mdl
——
分子量
946.761
InChiKey
RGWDEBDYPOAZAH-UHFFFAOYSA-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

  • 作为产物:
    描述:
    1,3-bis(4-acetylphenyl)triazene 、 bis-triphenylphosphine-palladium(II) chloride 在 triethylamine 作用下, 以 甲醇 为溶剂, 以68%的产率得到(1,3-bis(4-acetylphenyl)triaz-2-en-1-yl)bis(triphenyl-l5-phosphaneyl)palladium(IV) chloride
    参考文献:
    名称:
    Three-dimensional triazenido layers attained through classical and non-classical hydrogen interactions and its coordination to palladium under prolific occurrence of bifurcated hydrogen bonding
    摘要:
    The new ligand 1,3-bis(3-methoxy-4-methylbenzoate) triazene (1, bmmbt), and the already known ligand 1,3-bis(4-acetylphenyl)triazene (bapht), yield the two new palladium(II) complexes [(bmmbt)Pd(PPh3)(2)Cl]center dot DMSO (2) and [(bapht)Pd(PPh3)(2)Cl] (3) (Ph = phenyl; DMSO = dimethylsulfoxide). Compound 1 shows the existence of more than one interaction promoting the coupling between the triazene chains. Other remarkable types of interactions in 1 are bifurcated hydrogen contacts and non-classical CH center dot center dot center dot pi bonding. Complexes 2 and 3 present a planar geometry, supported also through bifurcated intramolecular Cl center dot center dot center dot H-C interactions, as well as the occurrence of trifurcated Cl center dot center dot center dot H-C intermolecular interactions. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2011.10.009
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