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2,2,6,6-tetramethyl-1-oxa-2-silacyclohexane

中文名称
——
中文别名
——
英文名称
2,2,6,6-tetramethyl-1-oxa-2-silacyclohexane
英文别名
2,2,6,6-tetramethyl-1,2-oxasilinane;2,2,6,6-Tetramethyloxasilinane
2,2,6,6-tetramethyl-1-oxa-2-silacyclohexane化学式
CAS
——
化学式
C8H18OSi
mdl
——
分子量
158.316
InChiKey
YAGZPYDVSRWLSB-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):
    2.78
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    2,2,6,6-tetramethyl-1-oxa-2-silacyclohexane 在 diphenyliodonium hexafluorophosphate 作用下, 以 二氯甲烷 为溶剂, 生成 [Dimethyl(4-methylpent-4-enyl)silyl]oxy-dimethyl-(4-methylpent-4-enyl)silane
    参考文献:
    名称:
    Oxasilacycles Leading to UV-Curable Polymers: Synthesis and Application
    摘要:
    Many applications of polymeric materials desire and in certain instances require various functions in one family of polymeric architectures. In this work, synthetic routes and methods to obtain novel oxasilacycles and their use in polymer chemistry as both monomer and cross-linking agents are presented. Photoacid generators are used for the acid-catalyzed ring-opening polymerization of the synthesized oxasilacycles allowing photoinitiated and controlled polymerizations. The polymerization behavior and influence of different photoacids as well as the influence of catalyst loading are examined using in situ IR spectroscopy. The synthesized cyclic structures offer a broad variety in polymer chemistry. Oxasilaspirocycles can either homopolymerize or function as a cross-linking reactant in organic polymers. A polystyrenehydroxyethyl methacrylate copolymer is cross-linked via polycondensation reactions of the oxasilaspirocycle. An isopropoxy-substituted oxasilamonocycle is synthesized for the modification of hydroxyl-terminated polydimethylsiloxanes for photoacid-initiated polymerizable telechelic structures. Additionally, the synthesis of multifunctional oligomers containing the photoacid generator unit and the cross-linking agent leads to highly cross-linked polydimethylsiloxane-based structures. In this system it is possible to predefine the gel content as well as the viscosity of the cross-linked polydimethylsiloxane after irradiation by the ratio of oxasilacycle to polydimethylsiloxane.
    DOI:
    10.1021/ma501857a
  • 作为产物:
    描述:
    参考文献:
    名称:
    Cai, Yudong; Roberts, Brian P., Journal of the Chemical Society. Perkin transactions I, 1998, # 3, p. 467 - 475
    摘要:
    DOI:
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文献信息

  • Cai, Yudong; Roberts, Brian P., Journal of the Chemical Society. Perkin transactions I, 1998, # 3, p. 467 - 475
    作者:Cai, Yudong、Roberts, Brian P.
    DOI:——
    日期:——
  • Oxasilacycles Leading to UV-Curable Polymers: Synthesis and Application
    作者:Christian A. Anger、Julian Kehrle、Konrad Hindelang、Jonathan G. C. Veinot、Jürgen Stohrer、Bernhard Rieger
    DOI:10.1021/ma501857a
    日期:2014.12.23
    Many applications of polymeric materials desire and in certain instances require various functions in one family of polymeric architectures. In this work, synthetic routes and methods to obtain novel oxasilacycles and their use in polymer chemistry as both monomer and cross-linking agents are presented. Photoacid generators are used for the acid-catalyzed ring-opening polymerization of the synthesized oxasilacycles allowing photoinitiated and controlled polymerizations. The polymerization behavior and influence of different photoacids as well as the influence of catalyst loading are examined using in situ IR spectroscopy. The synthesized cyclic structures offer a broad variety in polymer chemistry. Oxasilaspirocycles can either homopolymerize or function as a cross-linking reactant in organic polymers. A polystyrenehydroxyethyl methacrylate copolymer is cross-linked via polycondensation reactions of the oxasilaspirocycle. An isopropoxy-substituted oxasilamonocycle is synthesized for the modification of hydroxyl-terminated polydimethylsiloxanes for photoacid-initiated polymerizable telechelic structures. Additionally, the synthesis of multifunctional oligomers containing the photoacid generator unit and the cross-linking agent leads to highly cross-linked polydimethylsiloxane-based structures. In this system it is possible to predefine the gel content as well as the viscosity of the cross-linked polydimethylsiloxane after irradiation by the ratio of oxasilacycle to polydimethylsiloxane.
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