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cis-[PdCl2(bis[(3,5-dimethyl-1-pyrazolyl)methyl]ethylamine)]*CH2Cl2 | 914461-99-7

中文名称
——
中文别名
——
英文名称
cis-[PdCl2(bis[(3,5-dimethyl-1-pyrazolyl)methyl]ethylamine)]*CH2Cl2
英文别名
——
cis-[PdCl2(bis[(3,5-dimethyl-1-pyrazolyl)methyl]ethylamine)]*CH2Cl2化学式
CAS
914461-99-7
化学式
CH2Cl2*C14H23Cl2N5Pd
mdl
——
分子量
523.629
InChiKey
GFPMPQWFLUCRRF-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:
    Exploring the coordination chemistry and reactivity of hemilabile N-alkylaminopyrazole ligands towards Pd(II)
    摘要:
    Reaction of the N-alkylaminopyrazole (NN'N) ligands bis[(3,5-dimethyl-1-pyrazolyl)methyl]ethylamine (bdmae) and bis[(3,5dimethyl-1-pyrazolyl)methyl]isopropylamine (bdmai) with [PdCl2(CH3CN)(2)] in a 1:1 M/L ratio in CH2Cl2 produces cis-[PdCl2(NN'N)] (NN'N= bdmae (1), bdmai (2)). The solid state structure of complex 1 was determined by X-ray diffraction studies. The bdmae ligand is coordinated through the two N-pz atoms to the metal atom, which completes its coordination with two chlorine atoms in a cis disposition.Treatment of the corresponding ligand with [PdCl2(CH3CN)(2)] in 1: 1 M/L ratio in the presence of AgBF4 and metathesis with NaBPh4 in CH2Cl2/CH3OH (3:1) gave [PdCl(bdmae)](BPh4) (3), and in the presence of NaBPh4 in CH2Cl2/CH3CN (3:1) gave [PdCl(bdmai)](BPh4) (4). Complexes 1 and 2 were again obtained when complexes 3 and 4 were heated under reflux in a solution of Et4NCl in acetonitrile. These Pd(II) compounds were characterised by elemental analyses, conductivity measurements, IR, H-I and C-13{H-1} NMR, HMQC and NOESY spectroscopies. The NMR studies of the complexes prove the rigid conformation of the ligands when they are complexed. (c) 2006 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2006.05.046
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