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[PhC(NtBu)2Si(Cl){N2CH(SiMe3)}]2 | 1353880-94-0

中文名称
——
中文别名
——
英文名称
[PhC(NtBu)2Si(Cl){N2CH(SiMe3)}]2
英文别名
——
[PhC(NtBu)2Si(Cl){N2CH(SiMe3)}]2化学式
CAS
1353880-94-0
化学式
C38H66Cl2N8Si4
mdl
——
分子量
818.244
InChiKey
GIZXQYUGHGWAOH-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

反应信息

  • 作为产物:
    描述:
    N,N′-di-tertbutyl(phenylamidinato)chlorosilylene 、 三甲基硅烷化重氮甲烷正己烷 为溶剂, 以29.3%的产率得到[PhC(NtBu)2Si(Cl){N2CH(SiMe3)}]2
    参考文献:
    名称:
    A Remarkable End-On Activation of Diazoalkane and Cleavage of Both C–Cl Bonds of Dichloromethane with a Silylene to a Single Product with Five-Coordinate Silicon Atoms
    摘要:
    The 1:1 reaction of benzamidinato-stabilized chlorosilylene PhC(NtBu)(2)SiCl (1) with CH(SiMe3)N-2 resulted in the formation of colorless [PhC(NtBu)(2)Si(Cl){N2CH(SiMe3)}}(2) (2), which consists of a four-membered Si2N2 ring. Surprisingly, N-2 elimination from the diazoalkane did not occur, but rather an end-on activation of the nitrogen was observed. For the mechanism, we propose the formation of a silaimine complex A as an intermediate, which is formed during the reaction and dimerized under [2 + 2] cydoaddition to 2. In contrast, treatment of 1 with dichloromethane afforded a 2:1 product, [{PhC(NtBu)(2)Si(Cl-2)}(2)CH2} (3), which is obviously formed by oxidative addition under cleavage of both C-Cl bonds and formation of two Si-Cl and two Si-C bonds. Both silicon atoms in 3 are five-coordinate. Compounds 2 and 3 were characterized by single-crystal X-ray studies, multinuclear NMR spectroscopy, and El-mass spectrometry.
    DOI:
    10.1021/om201031n
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