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1,1,1,3,5,7,9,9,9-nonamethyl-3,5,7-trivinylpentasiloxane | 16545-47-4

中文名称
——
中文别名
——
英文名称
1,1,1,3,5,7,9,9,9-nonamethyl-3,5,7-trivinylpentasiloxane
英文别名
2,3,4-trivinyl-1,1,1,2,3,4,5,5,5-nonamethylpentasiloxane;3,5,7-trivinylnonamethylpentasiloxane;Nonamethyl-3,5,7-trivinylpentasiloxane;ethenyl-bis[(ethenyl-methyl-trimethylsilyloxysilyl)oxy]-methylsilane
1,1,1,3,5,7,9,9,9-nonamethyl-3,5,7-trivinylpentasiloxane化学式
CAS
16545-47-4
化学式
C15H36O4Si5
mdl
——
分子量
420.876
InChiKey
QUFRIPTUKDGBQG-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

物化性质

  • 沸点:
    135-136 °C(Press: 21 Torr)
  • 密度:
    0.904±0.06 g/cm3(Predicted)
  • 保留指数:
    1440.8

计算性质

  • 辛醇/水分配系数(LogP):
    5.11
  • 重原子数:
    24
  • 可旋转键数:
    11
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    36.9
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    9-乙酰基菲1,1,1,3,5,7,9,9,9-nonamethyl-3,5,7-trivinylpentasiloxaneRuH2(CO)(PPh3)3 作用下, 以 甲苯 为溶剂, 反应 70.0h, 以88.5%的产率得到2,3,4-tris[2-(9'-acetyl-10'-phenanthrenyl)ethyl]-1,1,1,2,3,4,5,5,5-nonamethylpentasiloxane
    参考文献:
    名称:
    Ruthenium-Catalyzed Chemical Modification of Poly(vinylmethylsiloxane) with 9-Acetylphenanthrene
    摘要:
    Poly [2-(9'-acetyl-10'-phenanthrenyl)ethylmethylsiloxane] (I) has been prepared by the activated dihydridocarbonyltris(triphenylphosphine)ruthenium (Ru)-catalyzed regioselective anti-Markovnikov addition of the 10-C-H bond of 9-acetylphenanthrene across the C-C double bonds of poly(vinylmethylsiloxane) (PVMS). This chemical modification of PVMS is highly efficient. The UV absorption, excitation, and emission spectral properties as well as the thermal properties of I have been studied. For comparison, the monomeric model systems tetrakis[2-(9'-acetyl-10'-phenanthrenyl)ethyldimethylsiloxy]silane (II), 2,3,4-tris[2-(9'-acetyl-10'-phenanthrenyl)ethyl-1,1,1,2,3,4,5,5,5-nonamethylpentasiloxane (III), and 9-acetyl-10-[2'-(trimethylsiloxydimethylsilyl)ethyl]phenanthrene (IV) were prepared by Ru-catalyzed reactions of 9-acetylphenanthrene with tetrakis [vinyldimethylsilyloxy]silane, 2,3,4-trivinyl-1,1,1,2,3,4,5,5,5-nonamethylpentasiloxane, and vinylpentamethyldisiloxane, respectively.
    DOI:
    10.1021/ma0119878
  • 作为产物:
    描述:
    六甲基二硅氧烷2,4,6-三乙烯基-2,4,6-三甲基环三硅氧烷三氟甲磺酸 作用下, 反应 0.33h, 以74.4%的产率得到1,1,1,3,5,7,9,9,9-nonamethyl-3,5,7-trivinylpentasiloxane
    参考文献:
    名称:
    Ruthenium-Catalyzed Chemical Modification of Poly(vinylmethylsiloxane) with 9-Acetylphenanthrene
    摘要:
    Poly [2-(9'-acetyl-10'-phenanthrenyl)ethylmethylsiloxane] (I) has been prepared by the activated dihydridocarbonyltris(triphenylphosphine)ruthenium (Ru)-catalyzed regioselective anti-Markovnikov addition of the 10-C-H bond of 9-acetylphenanthrene across the C-C double bonds of poly(vinylmethylsiloxane) (PVMS). This chemical modification of PVMS is highly efficient. The UV absorption, excitation, and emission spectral properties as well as the thermal properties of I have been studied. For comparison, the monomeric model systems tetrakis[2-(9'-acetyl-10'-phenanthrenyl)ethyldimethylsiloxy]silane (II), 2,3,4-tris[2-(9'-acetyl-10'-phenanthrenyl)ethyl-1,1,1,2,3,4,5,5,5-nonamethylpentasiloxane (III), and 9-acetyl-10-[2'-(trimethylsiloxydimethylsilyl)ethyl]phenanthrene (IV) were prepared by Ru-catalyzed reactions of 9-acetylphenanthrene with tetrakis [vinyldimethylsilyloxy]silane, 2,3,4-trivinyl-1,1,1,2,3,4,5,5,5-nonamethylpentasiloxane, and vinylpentamethyldisiloxane, respectively.
    DOI:
    10.1021/ma0119878
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文献信息

  • Syntheses of organofunctional siloxanes containing metal-ligating sidechains
    作者:Brian J. Brisdon、Andrew M. Watts
    DOI:10.1039/dt9850002191
    日期:——
    potential metal-ligating entities CHCH2, Ph, CN, cyclohexenyl, pyridine, and PPh2, n= 1 or 2) have been synthesised from commercially available dichlorosilanes by one of three procedures. The products are air-stable oils with the exception of the pyridine- and phosphine-functionalised compounds which react vigorously with oxygen, and the spectroscopic properties of corresponding organofunctional siloxanes
    通式为Me 3 SiO [SiMe(R)O] n SiMe 3的三,四和五硅氧烷的范围(R =乙烯基,n = 1-3; R =被潜在金属封端的烷基链-连接实体CH CH 2,Ph,CN,环己烯基,吡啶和PPh 2(n = 1或2)已通过三种方法之一由市售二氯硅烷合成。产物是空气稳定的油,除了吡啶和膦官能化的化合物与氧气剧烈反应外,相应的有机官能化硅氧烷的光谱性质非常相似,对n的依赖性很小。
  • Kopylov, V. M.; Agashkov, S. P.; Sunkovich, G. V., Journal of general chemistry of the USSR, 1991, vol. 61, # 6.2, p. 1257 - 1261
    作者:Kopylov, V. M.、Agashkov, S. P.、Sunkovich, G. V.、Prikhod'ko, P. L.
    DOI:——
    日期:——
  • Reaction of Organylchlorosilanes with Dimethyl Sulfoxide in the Presence of Octamethyltrisiloxane
    作者:S. V. Basenko、I. A. Gebel'、E. V. Boyarkina、M. G. Voronkov
    DOI:10.1023/b:rugc.0000042423.40451.86
    日期:2004.6
    Dichloro(methyl)(vinyl)silane reacts with DMSO in the presence of octamethyltrisiloxane to form cyclooligomethyl(vinyl)siloxanes(MeViSiO)(n) (n = 3-6). The reaction involves disproportionation of octamethyltrisiloxane into hexamethyldisiloxane and decamethyltetrasiloxane. Along with the latter two products, insertion products of methyl vinyl silanone into both permethyloligosiloxanes were identified. Alkyltrichlorosilanes RSiCl3 (R = Me, Et) react with DMSO in the presence of octamethyltrisiloxane to form cyclic oligoalkyltrichlorosiloxanes (RCISiO)(m) (m = 3-6).
  • Generation and capture of methyl(vinyl)silanone
    作者:S. V. Basenko、I. A. Gebel、M. G. Voronkov、L. V. Klyba、R. G. Mirskov
    DOI:10.1007/bf02495612
    日期:1998.8
    Methyl(vinyl)dichlorosilane reacts with DMSO in the presence of hexamethyldisiloxane to give the corresponding linear oligosiloxanes of the general formula Me3Si(OSiMeVin)(n)OSiMe3 (n = 1-6) as well as MeSi(OSiMe3)(3) and Me3Si(MeOSiVin)(m)OSi(OSiMe3)(Me)OSiMe3 (m = 1-2). The same reaction in the presence of chlorotrimethylsilane results in oligomers of the general formula Me3Si(OSiMeVin)(n)Cl (n = 1-3). A possible scheme of their formation is discussed.
  • Andrianov,K.A. et al., Journal of general chemistry of the USSR, 1968, vol. 38, p. 174 - 176
    作者:Andrianov,K.A. et al.
    DOI:——
    日期:——
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