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[(bis(N,N'-bis(2,6-diisopropylphenyl)acetamidinate)Zn2Et2]2O | 959419-16-0

中文名称
——
中文别名
——
英文名称
[(bis(N,N'-bis(2,6-diisopropylphenyl)acetamidinate)Zn2Et2]2O
英文别名
——
[(bis(N,N'-bis(2,6-diisopropylphenyl)acetamidinate)Zn2Et2]2O化学式
CAS
959419-16-0
化学式
C60H94N4OZn4
mdl
——
分子量
1148.99
InChiKey
MWOYKMUANUVJIP-UHFFFAOYSA-N
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:
    [DippNC(Me)NDipp]diethylzinc甲苯 为溶剂, 以44%的产率得到[(bis(N,N'-bis(2,6-diisopropylphenyl)acetamidinate)Zn2Et2]2O
    参考文献:
    名称:
    Mono- versus Bis-chelate Formation in Triazenide and Amidinate Complexes of Magnesium and Zinc
    摘要:
    Magnesium and zinc complexes of the monoanionic ligands N,N'-bis(2,6-di-isopropylphenyl)triazenide, L-1, N,N'-bis(2,6-di-isopropylphenyl)acetamidin ate, L-2, and N,N'-bis(2,6-di-isopropylphenyl)tert-butylamidinate, L-3, have been synthesized, but only L-3 possesses sufficient steric bulk to prevent bis-chelation. Hence, the reaction of (LH)-H-1 with excess ZnEt2 leads to the isolation of (L-1)(2)Zn, 1; (LH)-H-1 also reacts with BU2Mg in Et2O to afford (L-1)(2)Mg(Et2O), 2. Similar reactivity is observed for (LH)-H-2, leading to the formation of (L-2)(2)Zn, 3, and (L-2)(2)Mg, 4. The reaction of (LH)-H-2 with ZnR2 may also afford the tetranuclear aggregates {(L-2)Zn2R2}(2)O, 5 (R = Me) and 6 (R = Et). By contrast, the tert-butylamidinate ligand was found to exclusively promote mono-chelation, allowing (L-3)ZnCl(THF), 7, [(L-3)Zn(mu-Cl)](2), 8, (L-3)ZnN(SiMe3)(2), 9, (L-3)(MgPr)-Pr-i(Et2O), 10, and (L-3)(MgPr)-Pr-i(THF), 11, to be isolated. X-ray crystallographic analyses of 1, 2, 3, 4, 5, 6, 8, and 10 indicate that the capacity of L-3 to resist bis-chelation is due to greater occupation of the metal coordination sphere by the N-aryl substituents.
    DOI:
    10.1021/ic701061q
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