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trans-[PdCl2(P(OC6H3-2,4-tBu2)3)2] | 609368-10-7

中文名称
——
中文别名
——
英文名称
trans-[PdCl2(P(OC6H3-2,4-tBu2)3)2]
英文别名
——
trans-[PdCl2(P(OC6H3-2,4-tBu2)3)2]化学式
CAS
609368-10-7
化学式
C84H126Cl2O6P2Pd
mdl
——
分子量
1471.19
InChiKey
PTAZLHFIXGDUQY-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:
    参考文献:
    名称:
    The influence of steric bulk on the geometry of triarylphosphite-based palladacycles and their tricyclohexylphosphine adducts
    摘要:
    A range of complexes of the formula [PdCl2{P(OAr)(3)}(2)] have been synthesized in order to determine the effect of steric bulk on stereochemistry, one example [PdCl2{P(OC6H4-2-Bu-t)(3)}(2)] has been structurally characterized. Three palladacyclic complexes [{Pd(mu-Cl)-(kappa(2)-P, C-P(OC6H3R)(OC6H4R)(2))}(2)] have been synthesized (R = H, 2-Pr-t, 2-Bu-t) and two have been characterized by crystallography (R = H and Bu-t). The latter adopts the expected trans geometry while the former is cis. In this case, the driving force for the cis geometry seems to be intermolecular interactions in the crystal structure which are disrupted on substitution. We also report an unusual solvolysis reaction. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2005.11.014
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文献信息

  • Orthometallated palladium trimers in C–C coupling reactions
    作者:Izabela Błaszczyk、Andrzej Gniewek、Anna M. Trzeciak
    DOI:10.1016/j.jorganchem.2012.03.010
    日期:2012.7
    C–P(O–m-CH3C6H3)(O–m-CH3C6H4)2}2], 3b. The trimeric palladium complexes very efficiently catalyzed the Suzuki–Miyaura and Hiyama reactions in ethane-1,2-diol and the Sonogashira cross-coupling in ionic liquids. The mercury test confirmed the homogeneous pathway of the Suzuki–Miyaura reaction, although Pd(0) nanoparticles were observed by TEM in the post-reaction mixture.
    制备了一系列[Pd 3(μ-Cl)4(PC )2 ](PC =正属化的亚磷酸芳基亚磷酸酯)的三聚配合物,并使用31 P NMR和ESI-MS方法对其结构进行了表征。的结构[3(μ 2 -Cl)4 ķ 2 -P,C-P(O-O-CH 3 C ^ 6 ħ 3)(O-O-CH 3 C ^ 6 ħ 4)2 } 2 ] ,1C,通过X射线衍射确定。将其与二聚体复合物[Pd 2(μ-Cl)2 k 2 -P,C–P(O–m-CH 3 C 6 H 3)(O–m-CH 3 C 6 H 4)2 } 2 ],3b。三聚体络合物非常有效地催化了乙烷-1,2-二醇中的Suzuki-Miyaura和Hiyama反应,以及离子液体中的Sonogashira交叉偶联。尽管通过TEM在反应后混合物中观察到Pd(0)纳米颗粒,但测试证实了Suzuki-Miyaura反应的均质途径。
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