摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

octakis(tert-butyldimethylsilyl)pentacyclo[4.2.0.02,5.03,8.04,7]octasilane | 121403-88-1

中文名称
——
中文别名
——
英文名称
octakis(tert-butyldimethylsilyl)pentacyclo[4.2.0.02,5.03,8.04,7]octasilane
英文别名
octakis-(t-butyldimethylsilyl)pentacyclo<4.2.0.02,5.03,8.04,7>octasilane;Octakis(tertbutyldimethylsilyl)octasilacubane;tert-butyl-[2,3,4,5,6,7,8-heptakis[tert-butyl(dimethyl)silyl]-1,2,3,4,5,6,7,8-octasilapentacyclo[4.2.0.02,5.03,8.04,7]octan-1-yl]-dimethylsilane
octakis(tert-butyldimethylsilyl)pentacyclo[4.2.0.0<sup>2,5</sup>.0<sup>3,8</sup>.0<sup>4,7</sup>]octasilane化学式
CAS
121403-88-1
化学式
C48H120Si16
mdl
——
分子量
1146.85
InChiKey
NHIAOHVJRBRJNE-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):
    17.28
  • 重原子数:
    64
  • 可旋转键数:
    16
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    octakis(tert-butyldimethylsilyl)pentacyclo[4.2.0.02,5.03,8.04,7]octasilane间氯过氧苯甲酸 作用下, 以 为溶剂, 反应 168.0h, 以98%的产率得到1,3,5,7,9,11,13,15-octakis(tert-butyldimethylsilyl)pentacyclo[9.5.1.13,9.15,15.17,13]octasiloxane
    参考文献:
    名称:
    Structure and oxidation of octakis(tert-butyldimethylsilyl)octasilacubane
    摘要:
    The molecular structure of the silyl-substituted octasilacubane [(t-BuMe2Si)Si](8) (1) was analyzed by X-ray crystallography, and the structural parameters (bond length and angles) were compared with those of the alkyl- and aryl-substituted octasilacubanes. A thermogravimetric analysis revealed that 1 remained stable under argon up to 300 degreesC, indicating that 1 is much more thermally stable than alkyl-substituted (ThexSi)8 (Thex = 1,1,2-trimethylpropyl) (2), which decomposed at 200 degreesC. Although compound 1 is stable in the air, 1 reacted with m-chloroperoxybenzoic acid (mCPBA). Thus, treatment of 1 with fourteen equivalents of mCPBA led to the formation of octakis(tert-butyldimethylsilylsilsesquioxane) (3) in 98% yield. The structure of 3 was also established by X-ray crystallography, indicating that all the oxygen atoms inserted into the Si-Si bonds of the Si-8 framework and the exocyclic Si-Si bonds remained intact under the conditions employed. Compound 3 is the first example of silsesquioxane with bulky silyl substituents, and shows relatively intense absorptions in the UV region. (C) 2003 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0022-328x(03)00288-2
  • 作为产物:
    描述:
    Tert-butyl-[[[tert-butyl(dimethyl)silyl]-dichlorosilyl]-dichlorosilyl]-dimethylsilane 生成 octakis(tert-butyldimethylsilyl)pentacyclo[4.2.0.02,5.03,8.04,7]octasilane
    参考文献:
    名称:
    NAGAI, JOITIRO;MATSUMOTO, XIDEHYUKI;KOIKEH, XITOSI;NAOI, JOSITAKEH
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • The first octasilacubane system: synthesis of octakis-(t-butyldimethylsilyl)pentacyclo[4.2.0.02,5.03,8.04,7]octasilane
    作者:Hideyuki Matsumoto、Koichi Higuchi、Yoshinori Hoshino、Hitoshi Koike、Yoshitake Naoi、Yoichiro Nagai
    DOI:10.1039/c39880001083
    日期:——
    The first octasilacubane, octakis-(t-butyldimethylsilyl)pentacyclo[4.2.0.02,5.03,8.04,7]octasilane, was synthesised in one step by condensation of 2,2,3,3-tetrabromo-1,4-di-t-butyl-1,1,4,4-tetramethyltetrasilane or 1,1,1-tribromo-2-t-butyl-2,2-dimethyldisilane with sodium in toluene.
    通过将2,2,3,3-四-缩合反应一步合成了第一个八铝氧,辛基-(叔丁基二甲基甲硅烷基)五环[4.2.0.0 2,5 .0 3,8 .0 4,7 ]八硅烷。 1,4-二叔丁基-1,1,4,4-四甲基四硅烷或1,1,1-三-2-叔丁基-2,2-二甲基乙硅烷甲苯溶液。
  • CHEM.-ZTG., 113,(1989) N, C. 167
    作者:
    DOI:——
    日期:——
  • MATSUMOTO, HIDEYUKI;HIGUCHI, KOICHI;HOSHINO, YOSHINORI;KOIKE, HITOSCHI;NA+, J. CHEM. SOC. CHEM. COMMUN.,(1988) N 16, C. 1083-1084
    作者:MATSUMOTO, HIDEYUKI、HIGUCHI, KOICHI、HOSHINO, YOSHINORI、KOIKE, HITOSCHI、NA+
    DOI:——
    日期:——
查看更多