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[2,6-bis(4,4-dimethyl-2-oxazolinyl)phenyl]chloropalladium | 945657-56-7

中文名称
——
中文别名
——
英文名称
[2,6-bis(4,4-dimethyl-2-oxazolinyl)phenyl]chloropalladium
英文别名
[PdCl(2,6-bis(oxazolinyl)phenyl)]
[2,6-bis(4,4-dimethyl-2-oxazolinyl)phenyl]chloropalladium化学式
CAS
945657-56-7
化学式
C16H19ClN2O2Pd
mdl
——
分子量
413.212
InChiKey
YBGNHQYZCCNTNK-UHFFFAOYSA-M
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:
    trans-bromo(2,6-dicarboxyphenyl)bis(triphenylphosphine)palladium2-氨基-2-甲基-1-丙醇草酰氯甲基磺酰氯三乙胺 作用下, 以 二氯甲烷N,N-二甲基甲酰胺 为溶剂, 以48%的产率得到[2,6-bis(4,4-dimethyl-2-oxazolinyl)phenyl]chloropalladium
    参考文献:
    名称:
    Synthesis of [2,6-Bis(2-oxazolinyl)phenyl]palladium Complexes via the Ligand Introduction Route
    摘要:
    A series of [2,6-bis(2-oxazolinyl)phenyl]palladium (Phebox-Pd) complexes were synthesized via the ligand introduction route. trans-Bromo(2,6-dicarboxyphenyl)bis(triphenylphosphine)palladium was prepared by the reaction of 2-bromoisophthalic acid with Pd(PPh3)(4) in 93% yield, and the carboxy groups of the palladium complex were converted into oxazolinyl groups to give the Phebox-Pd complexes in 44-57% yield.
    DOI:
    10.1021/om800666x
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文献信息

  • A new, easily recyclable arylating agent based on a diphosphino-digold(i) complex
    作者:Marianne Stol、Dennis J. M. Snelders、Huub Kooijman、Anthony L. Spek、Gerard P. M. van Klink、Gerard van Koten
    DOI:10.1039/b701271c
    日期:——
    The synthesis of two organogold(I) complexes, [(Au(NCN))2(dppbp)] (6) and [(Au(Phebox))2(dppbp)] (9), and their application in subsequent transmetalating reactions are described. A trinuclear organogold(I) complex, [(AuCl)3(tdpppb)] (4) is also reported, which exhibits a surprisingly high solubility in dichloromethane. It was found that 6 and 9 can cleanly transfer the anionic NCN-([C6H3(CH2NMe2)2-2,6]−) or Phebox-([2,6-bis(oxazolinyl)phenyl]−) moiety to TiIV and PdII centers, respectively. The coproduct [(AuCl)2(dppbp)] (3, dppbp is [4-Ph2PC6H4]2 (1)) formed during this transmetalation reaction, precipitates almost quantitatively from the reaction mixture (toluene) and can thus be separated by simple filtration. In comparison, [AuCl(PPh3)], formed as the coproduct in the transmetalation reaction of [Au(NCN)(PPh3)] with metal salts, has a higher solubility in apolar solvents and thus is more difficult to separate from the resultant organometallic complex. Digold complex 6 has been characterized by NMR spectroscopy and crystallographic analyses. These analyses show that the two gold units are essentially independent. The formation of a dimetallic transmetalating agent based on gold(I) had no effect on its transmetalating properties.
    本文介绍了两种有机(I)配合物 [(Au(NCN))2(dppbp)] (6) 和 [(Au(Phebox))2(dppbp)] (9) 的合成及其在随后的反属化反应中的应用。报告还介绍了一种三核有机(I)配合物[(AuCl)3(tdpppb)] (4),它在二氯甲烷中的溶解度之高令人惊讶。研究发现,6 和 9 可以分别将阴离子 NCN-([C6H3(CH2NMe2)2-2,6]-)或 Phebox-([2,6-双(恶唑啉基)苯基]-)分子干净地转移到 TiIV 和 PdII 中心。在这一跨属化反应中形成的副产物[(AuCl)2(dppbp)](3,dppbp 为 [4-Ph2PC6H4]2 (1))几乎定量地从反应混合物(甲苯)中析出,因此只需简单过滤即可分离。相比之下,在[Au(NCN)(PPh3)]与属盐的反属反应中形成的副产物[AuCl(PPh3)]在非极性溶剂中的溶解度较高,因此更难从生成的有机属复合物中分离出来。Digold 复合物 6 已通过核磁共振光谱和晶体学分析进行了表征。这些分析表明,两个单元基本上是独立的。以(I)为基础形成的二属透属剂对其透属特性没有影响。
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