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trans-di-μ-dichlorodibis(4-diphenylphosphanequinoline)di-palladium(II) | 1021148-65-1

中文名称
——
中文别名
——
英文名称
trans-di-μ-dichlorodibis(4-diphenylphosphanequinoline)di-palladium(II)
英文别名
——
trans-di-μ-dichlorodibis(4-diphenylphosphanequinoline)di-palladium(II)化学式
CAS
1021148-65-1
化学式
C42H32Cl4N2P2Pd2
mdl
——
分子量
981.329
InChiKey
ANVVVMAGMDRXLY-UHFFFAOYSA-J
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:
    dichloro(cycloocta-1,5-diene)palladium (II)4-(diphenylphosphanyl)quinoline二氯甲烷 为溶剂, 以63.2%的产率得到trans-di-μ-dichlorodibis(4-diphenylphosphanequinoline)di-palladium(II)
    参考文献:
    名称:
    Palladium(II) complexes of 2-, 3-, and 4-quinolinyl(diphenyl)phosphane and di-(3-quinolinyl)phenylphosphane: Synthesis, characterization, and catalytic screening
    摘要:
    One previously known and three novel quinolinyl phosphanes were synthesized by either a reaction between a lithiated diphenylphosphane and the appropriate chloroquinoline or by a reaction between a lithiated haloquinoline and an arylchlorophosphane. The reaction of the quinolinyl phenylphosphane ligands with PdCl2(cod) produced monomeric palladium complexes in diethyl ether and dimeric, chlorine-bridged complexes in dichloromethane. Crystal structures of the palladium complexes confirm that the quinolinyl phenylphosphanes do not form chelated structures while bonded to the metal centre. 2-Quinolinyl(diphenyl) phosphane has a tendency to form a cis-isomer while bonded to the metal centre in the mononuclear complex due to attractive interactions between two ligands. A catalytic study showed that the quinolinyl phenylphosphane ligands are moderately active in the Suzuki-Miyaura coupling of various aryl halides in air. (C) 2007 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2007.09.009
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