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1,3-diisopropoxyhexamethyltrisilane | 136246-82-7

中文名称
——
中文别名
——
英文名称
1,3-diisopropoxyhexamethyltrisilane
英文别名
——
1,3-diisopropoxyhexamethyltrisilane化学式
CAS
136246-82-7
化学式
C12H32O2Si3
mdl
——
分子量
292.641
InChiKey
CJIDSDBDFGYONH-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):
    4.11
  • 重原子数:
    17.0
  • 可旋转键数:
    6.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    18.46
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    描述:
    2-异氰基-1,3-二异丙基苯1,3-diisopropoxyhexamethyltrisilane 在 palladium diacetate 作用下, 以 甲苯 为溶剂, 反应 14.0h, 以51%的产率得到2,5-diisopropoxy-3-<(2,6-diisopropylphenyl)imino>-2,4,4,5-tetramethyl-2,4,5-trisilahexane
    参考文献:
    名称:
    Palladium-catalyzed insertion of isocyanides into the silicon-silicon linkages of oligosilanes
    摘要:
    Full details of a study on the reactions of oligosilanes with isocyanides promoted by a palladium catalyst are described. Heating a mixture of oligosilanes and excess 2,6-disubstituted aryl isocyanide in the presence of palladium(II) acetate led to the complete insertion of isocyanide into all silicon-silicon linkages, giving oligo(silylimine) derivatives. The oligo(silylimine)s have been isolated and characterized so far in the complete insertion reaction with oligosilanes up to a hexasilane. Use of the limiting amount of isocyanide permitted insertion of isocyanide into predominantly the terminal silicon-silicon linkages. The mode of the insertion reaction depends on the substituent at the silicon, e.g., tetrasilanes with phenyl groups on the internal silicon atoms favorably underwent the insertion reaction at the terminal silicon-silicon linkages, resulting in the partial insertion. The bulkiness of the ortho substituents on the aromatic isocyanide was also found to have much influence on the insertion; hence, 2,6-diisopropylphenyl isocyanide favored the partial insertion. New skeletal rearrangement of oligosilanes took place in a palladium-catalyzed reaction of substituted aryl isocyanide with tetra- and hexasilanes, forming 3,3-bis(silyl)-l-aza-2, 4-disilacyclobutane derivatives. The rearrangement, which is unique and intriguing in that the product is properly reconstituted from four fragments of the tetrasilane and two fragments of the isocyanide, was promoted in the copresence of a tert-alkyl isocyanide.
    DOI:
    10.1021/ja00023a043
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