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Zn(N-(1-(pyridin-2-yl)ethylidene)ethane-1,2-diamine)Cl2 | 248256-51-1

中文名称
——
中文别名
——
英文名称
Zn(N-(1-(pyridin-2-yl)ethylidene)ethane-1,2-diamine)Cl2
英文别名
——
Zn(N-(1-(pyridin-2-yl)ethylidene)ethane-1,2-diamine)Cl2化学式
CAS
248256-51-1
化学式
C9H13Cl2N3Zn
mdl
——
分子量
299.518
InChiKey
ASOZXMMARDIZKC-CYXWJPPTSA-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:
    描述:
    zinc(II) chloride 、 N,N'-bis(1-(pyridin-2-yl)ethylidene)ethane-1,2-diamine乙醇 为溶剂, 以40%的产率得到Zn(N-(1-(pyridin-2-yl)ethylidene)ethane-1,2-diamine)Cl2
    参考文献:
    名称:
    Zinc(II) complexes derived from the di-Schiff-base ligand N,N′-bis[1-(pyridin-2-yl)ethylidene]ethane-1,2-diamine (LA) and its hydrolytic-cleavage product N-[1-pyridin-2-yl)ethylidene]ethane-1,2-diamine (L): preparation, characterization and crystal structure of the 5-coordinate species [ZnLCl2]
    摘要:
    The reactions of ZnX2 (X=Cl, Br) with the di-Schiff-base ligand N,N'-bis[1-(pyridin-2-yl)ethylidene]ethane-1,2-diamine (L-A) were studied. The chemical identity of the products is solvent-dependent. The reactions in tetrahydrofuran give complexes [ZnLACl2] (I) and [ZnLABr2] (2). Treatment of L-A with an equimolar, or excess, amount of ZnX2 in ethanol yields the five-coordinate complexes [ZnLCl2] (3) and [ZnLBr2] (4), where L is the mono-Schiff base N-[1-pyridin-2-yl)ethylidene]-ethane-1,2-diamine complexes 3 and 4 have resulted from hydrolytic cleavage of the precursor di-Schiff base L-A. These two complexes can also be prepared in one step and in good yield by the reactions of ZnX2 with 2 acetylpyridine and ethane-1,2-diamine in refluxing methanol. The X-ray structure of 3 demonstrates that L behaves as a tridentate chelate with the ligated atoms being the pyridine, methine and amino nitrogens; two terminal, equatorial chlorides complete five-coordination at zinc(II). The new complexes 1-4 were characterized by elemental analyses and spectroscopic (IR, far-IR,H-1 NMR) techniques. It is proposed that L-A behaves as a tetradentate chelate in complexes 1 and 2, for which a monomeric pseudo-octahedral stereochemistry with trans chloro ligands is assigned in the solid state. All data are discussed in terms of the nature of bonding and known or assigned structures. (C) 1999 Elsevier Science Ltd. All nights reserved.
    DOI:
    10.1016/s0277-5387(99)00141-2
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