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(μ-Br)2[κ(2)-N2',C1-1-Pd-2-((2'-NH2C6H4)C6H4)]2 | 182628-73-5

中文名称
——
中文别名
——
英文名称
(μ-Br)2[κ(2)-N2',C1-1-Pd-2-((2'-NH2C6H4)C6H4)]2
英文别名
(μ-Br)2[Pd(κ2-N2',C1-2-(2'-NH2C6H4)C6H4)]2
(μ-Br)2[κ(2)-N2',C1-1-Pd-2-((2'-NH2C6H4)C6H4)]2化学式
CAS
182628-73-5
化学式
C24H20Br2N2Pd2
mdl
——
分子量
709.084
InChiKey
RPMIJUBBLONMGE-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

  • 作为反应物:
    描述:
    (μ-Br)2[κ(2)-N2',C1-1-Pd-2-((2'-NH2C6H4)C6H4)]21,4-dimethyl but-2-enedioate氯仿 为溶剂, 生成 (μ-Br)2[κ(2)-N2',C1-1-Pd-2-((2'-NH2C6H4)C6H4)-cis-1,2-(CO2Me)2-C=C]2
    参考文献:
    名称:
    Monoinsertion of but-2-ynedioic acid dimethyl ester into palladium–carbon σ bonds of cyclopalladated compounds derived from biphenyl-2-ylamine: X-ray molecular structure of biphenyl-2-yl-(2,4,6-trimethoxy-benzylidene)-amine
    摘要:
    Dinuclear cyclopalladated compounds (mu-Br)2[kappa(2)-N2',Cl-1-Pd-2-{(2'-RCH=NC6H4)C6H4}](2) [1a (R = 2,4,6-trimethoxyphenyl), 1b (R = 2,6-dichlorophenyl) and 1c (R = 2,6-difluorophenyl)] and (mu-Br)(2)[kappa(2)-N-2',Cl-1-Pd-2-{(2'-NH2C6H4)C6H4}](2) (1d) reacted with but-2-ynedioic acid dimethyl ester (molar ratio 1-2) to afford the dinuclear cyclopalladated compounds (mu-Br)(2)[kappa(2)-N2',Cl-1-Pd-2-{(2'-RCH=NC6H4)C6H4}-cis-1,2-(CO2Me)(2)-C=C](2) [2a (R = 2,4,6-trimethoxyphenyl), 2b (R = 2,6-dichlorophenyl) and 2c (R = 2,6-difluorophenyl)] and (mu-Br)(2)[kappa(2)-N2',Cl-1-Pd-2-{(2'-NH2C6H4)C6H4}-cis-1,2-(CO2Me)(2)-C=C](2) (2d), which derived from the monoinsertion of the alkyne into the palladium-carbon sigma bonds of the cyclopalladated dimers 1. Compounds 2a and 2b reacted with PPh3 (molar ratio 1-4) to give a mixture of the mononuclear compound trans-N,P-{[kappa(2)-N2',Cl-1-Pd-2-{(Z-2'-RCH=NC6H4)C6H4}-cis-1,2-(CO2Me)(2)-C=C]Br(PPh3)} and trans-P,P-{[kappa(1)-Cl-1-Pd-2-{(E-2'-RCH=NC6H4)C6H4)-cis-1,2(CO2Me)(2)-C=C]Br(PPh3)(2)} in a molar ratio of 1-2 and ca. 1-12, respectively. Compound 2c reacted with PPh3 in a molar ratio 1-4 giving trans-P,P-{[kappa(1)-Cl-1-Pd-2-{(E-2'-RCH=NC6H4)C6H4}-cis-1,2-(CO2Me)(2)-C=C]Br(PPh3)(2)} (R=2,6-difluorophenyl)-(compound 4c) and compound 2d reacted with PPh3 in a molar ratio of 1-2, affording the mononuclear cyclopalladated compound trans-N,P-{[cis-kappa(2) -N2',Cl-1-Pd-2-{(2'-NH2C6H4)C6H4}-1,2-(CO2Me)(2)-C=C]Br(PPh3)} (compound 3d). Notably, the P-31{H-1} NMR of compounds 4 produced an AB spin system, showing that compounds 4 were chiral. In addition, we report the X-ray molecular structure of the E isomer of the free Schiff base a [biphenyl-2-yl-(2,4,6-trimethoxy-benzylidene)-amine]. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2005.08.002
  • 作为产物:
    描述:
    palladium diacetate 、 2-氨基联苯 、 lithium bromide 以 溶剂黄146丙酮 为溶剂, 以39%的产率得到(μ-Br)2[κ(2)-N2',C1-1-Pd-2-((2'-NH2C6H4)C6H4)]2
    参考文献:
    名称:
    再谈2-苯基苯胺的环钯反应
    摘要:
    2-苯基苯胺与甲苯中的Pd(OAc)2在室温下以一对一的摩尔比反应24小时,并与PdCl 2,NaCl和NaOAc体系以1(2-苯基苯胺):1(PdCl 2):2(氯化钠):1(的NaOAc)在甲醇中在室温下1周,得到双核环钯化合物(μ-X摩尔比)2 [{钯κ 2 - N2 ',C1 -2-(2'- NH 2 C 6 H 4)C 6 H 4 }] 2 [ 1a(X = OAc)和1b(X = Cl)]高产率。此外,2-苯基苯胺与Pd(OAc)之间的反应2在60℃下4小时在酸乙酸一个对一摩尔比,然后用溴化锂的复分解反应时,双核环钯化合物的允许隔离(μ-溴)2 [钯{κ 2 - N2 ',C1 -2-(2'-NH 2 C 6 H 4)C 6 H 4 }] 2(1c)以中等收率。并行处理,但使用monodeuterated乙酸(DOAc)如在cyclopalladation反应溶剂,化合物的混合物的允许隔离1C,1C
    DOI:
    10.1016/j.jorganchem.2004.07.067
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