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(N,N'-tetramethylethylenediamine)Zn(SSiMe3)2 | 858943-56-3

中文名称
——
中文别名
——
英文名称
(N,N'-tetramethylethylenediamine)Zn(SSiMe3)2
英文别名
(N,N'-tmeda)Zn(SSiMe3)2
(N,N'-tetramethylethylenediamine)Zn(SSiMe3)2化学式
CAS
858943-56-3
化学式
C12H34N2S2Si2Zn
mdl
——
分子量
392.108
InChiKey
CFUXJGJHPYDCFO-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

  • 作为反应物:
    描述:
    四甲基乙二胺(N,N'-tetramethylethylenediamine)Zn(SSiMe3)2zinc diacetate二氯甲烷 为溶剂, 以45%的产率得到[(N,N,N',N'-tetramethylethylenediamine)6Zn14S13Cl2]
    参考文献:
    名称:
    Zinc Chalcogenolate Complexes as Precursors to ZnE and Mn/ZnE (E = S, Se) Clusters
    摘要:
    The ternary clusters (tmeda)(6)Zn14-xMnxS13Cl2 (1a-d) and (tmeda)(6)Zn14-xMnxSe13Cl2 (2a-d), (tmeda = N,N,N',N'-tetramethylethylenediamine; x approximate to 2-8) and the binary clusters (tmeda)(6)Zn14E13Cl2 (E = S, 3; Se, 4;) have been isolated by reacting (tmeda)Zn(ESiMe3)(2) with Mn(II) and Zn (II) salts. Single crystal X-ray analysis of the complexes confirms the presence of the six "(tmeda)ZnE2" units as capping ligands that stabilize the clusters, and distorted tetrahedral geometry around the metal centers. Mn(II) is incorporated into the ZnE framework by substitution of Zn(II) ions in the cluster. The polynuclear complexes (tmeda)(6)Zn12.3Mn1.7S13Cl2 1a, (tmeda)(6)Zn12.0Mn2.0Se13Cl2 2a, and (tmeda)(6)Zn8.4Mn5.6Se13Cl2 2d represent the first examples of "Mn/ZnE" clusters with structural characterization and indications of the local chemical environment of the Mn(II) ions. The incorporation of higher amounts of Mn into 1d and 2d has been confirmed by elemental analysis. Density functional theory (DFT) calculations indicate that replacement of Zn with Mn is perfectly feasible and at least partly allows for the identification of some sites preferred by the Mn(II) metals. These calculations, combined with luminescence studies, suggest a distribution of the Mn(II) in the clusters. The room temperature emission spectra of clusters 1c-d display a significant red shift relative to the all zinc cluster 3, with a peak maximum centered at 730 nm. Clusters 2c-d display a peak maximum at 640 nm in their emission spectra.
    DOI:
    10.1021/ic200307g
  • 作为产物:
    描述:
    双(三甲基硫化硅)四甲基乙二胺zinc diacetate四氢呋喃 为溶剂, 以94%的产率得到(N,N'-tetramethylethylenediamine)Zn(SSiMe3)2
    参考文献:
    名称:
    Coordination Complexes of Zinc with Reactive ESiMe3 (E = S, Se, Te) Ligands
    摘要:
    The complexes (N,N'-tmeda)Zn(ESiMe3)(2) (E = S, 1a; E = So, 2a; E = Te, 3a) and (3,5-Me-2-C5H3N)(2)Zn(ESiMe3)(2) (E = S, 1b; E = Se, 2b; E = Te, 3b) have been prepared in high yield by the reaction of E(SiMe3)(2) with (N,N'-tmeda)Zn(OAc)(2) (4a) and (3,5-Me-2-C5H3N)(2)Zn(OAc)(2) (4b), respectively. Complexes 1-3 have been characterized spectroscopically and by means of single-crystal X-ray diffraction. All six complexes exist in the solid state as monomeric species with terminally bonded trimethylsilylchalcogenolate moieties and a distorted tetrahedral geometry of the zinc center.
    DOI:
    10.1021/om050088v
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