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1,1',2,2'-(HAlNMe3)2(NSiMe2NSiMe2N(H)SiMe2)2 | 332416-95-2

中文名称
——
中文别名
——
英文名称
1,1',2,2'-(HAlNMe3)2(NSiMe2NSiMe2N(H)SiMe2)2
英文别名
——
1,1',2,2'-(HAlNMe3)2(NSiMe2NSiMe2N(H)SiMe2)2化学式
CAS
332416-95-2
化学式
C18H58Al2N8Si6
mdl
——
分子量
609.188
InChiKey
XWRDTSJOUXJVDS-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:
    trimethylamine alane六甲基环三硅氮烷甲苯 为溶剂, 以21%的产率得到1,1',2,2'-(HAlNMe3)2(NSiMe2NSiMe2N(H)SiMe2)2
    参考文献:
    名称:
    Novel Aluminum Hydride Derivatives from the Reaction of H3Al·NMe3 with the Cyclosilazanes [Me2SiNH]3 and [Me2SiNH]4
    摘要:
    The amine hydrogen atoms of the cyclic trimeric silazane [Me2SiNH](3) are readily replaced by the H2Al . NMe3 group in a simple aminolyis reaction of [Me2SiNH](3) with H3Al . NMe3 to afford the aluminum amides (Me2SiNAlH2. NMe3)(n)(Me2SiNH)(3-n) (1, n = 3; 2, n = 1; 4, n = 2). The monosubstituted amide 2 could not be isolated, because it undergoes condensation to the tricyclic compound 1,1',2,2'-(HAlMe3)(2) (NSiMe2NSiMe2N(H)SiMe2)(2) (3). Contrary to these results the analogous reactions of the more flexible cyclic tetrameric silazane [Me2SiNH](4) with H3Al . NMe3 did not give simple aluminum amides, but complicated mixtures were obtained from which the interesting polycyclic species Al5C22H73N10S18.C6H6 (5) and Al6C22H76N10Si8.1/4 C6H14 (6) could be isolated in low yields. A key step in the formation of 5 and 6 is a low-temperature dehydrosilylation reaction which leads to cleavage of the silazane ring. Compounds 1, 3, and 4 were characterized spectroscopically (H-1, C-13, Al-27 NMR and FTIR) and by single crystal X-ray diffraction, whereas 5 and 6 were characterized by X-ray diffraction only. Thermolysis experiments involving 1 and 3 indicate that the onset of Al-N bond formation via dehydrosilylation is accompanied by loss of trimethylamine and formation of larger aggregates, which are stable to further silane elimination to at least 620 degreesC.
    DOI:
    10.1021/ic000636r
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