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4-[3,5-Bis[2-[2,5-didecoxy-4-[2-[2,5-didecoxy-4-[2-tri(propan-2-yl)silylethynyl]phenyl]ethynyl]phenyl]ethynyl]phenyl]buta-1,3-diynyl-trimethylsilane | 1211509-63-5

中文名称
——
中文别名
——
英文名称
4-[3,5-Bis[2-[2,5-didecoxy-4-[2-[2,5-didecoxy-4-[2-tri(propan-2-yl)silylethynyl]phenyl]ethynyl]phenyl]ethynyl]phenyl]buta-1,3-diynyl-trimethylsilane
英文别名
——
4-[3,5-Bis[2-[2,5-didecoxy-4-[2-[2,5-didecoxy-4-[2-tri(propan-2-yl)silylethynyl]phenyl]ethynyl]phenyl]ethynyl]phenyl]buta-1,3-diynyl-trimethylsilane化学式
CAS
1211509-63-5
化学式
C147H230O8Si3
mdl
——
分子量
2209.69
InChiKey
QUXIDMHEFDBPQC-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):
    43.81
  • 重原子数:
    158
  • 可旋转键数:
    101
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.69
  • 拓扑面积:
    73.8
  • 氢给体数:
    0
  • 氢受体数:
    8

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
  • 下游产品
    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:
    4-[3,5-Bis[2-[2,5-didecoxy-4-[2-[2,5-didecoxy-4-[2-tri(propan-2-yl)silylethynyl]phenyl]ethynyl]phenyl]ethynyl]phenyl]buta-1,3-diynyl-trimethylsilanepotassium carbonate 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 1.0h, 以91%的产率得到2-[4-[2-[4-[2-[3-Buta-1,3-diynyl-5-[2-[2,5-didecoxy-4-[2-[2,5-didecoxy-4-[2-tri(propan-2-yl)silylethynyl]phenyl]ethynyl]phenyl]ethynyl]phenyl]ethynyl]-2,5-didecoxyphenyl]ethynyl]-2,5-didecoxyphenyl]ethynyl-tri(propan-2-yl)silane
    参考文献:
    名称:
    Conjugated Oligoyne-Bridged [60]Fullerene Molecular Dumbbells: Syntheses and Thermal and Morphological Properties
    摘要:
    A series of linear and star-shaped pi-conjugated oligomer hybrids (2-5) composed of an oligoyne core, ranging from 1,3-butadiyne to 1,3,5.7,9,11-dodecahexayne, and fullerenyl end-capping groups has been synthesized and studied. The molecular structures of these fullerene-oligoyne hybrids were assembled through three key reactions. Pd-catalyzed cross-coupling, Cu-catalyzed oxidative homocoupling, and an in situ alkynylation reaction on [60]fullerene. The properties of these compound were investigated by UV-vis spectroscopy, differential scanning calorimetry (DSC), and atomic force microscopy (AFM) with the purpose of understanding the thermal reactivity arising from the oliogyne moieties as well as the morphological properties on surface. Our study shows that these fullerene-oliogyne hybrids tend to aggregate in different morphologies, including nanospheres, nanoflakes, and continuous thin films, while the morphological properties appear to be subject to the influence of molecular factors such as oligomer chain length, solubilizing alkylphenyl groups, and the thermal reactivity of the oligoyne unit. The correlation between molecular property and interfacial aggregation behavior evinced by these fullerene-oligoyne hybrids suggests a viable approach to exert bottom-up control over the structures and properties of fullerene based nanomaterials.
    DOI:
    10.1021/jo9021748
  • 作为产物:
    描述:
    2-[2,5-Didecoxy-4-[2-[2,5-didecoxy-4-[2-[3-[2-[2,5-didecoxy-4-[2-[2,5-didecoxy-4-[2-tri(propan-2-yl)silylethynyl]phenyl]ethynyl]phenyl]ethynyl]-5-ethynylphenyl]ethynyl]phenyl]ethynyl]phenyl]ethynyl-tri(propan-2-yl)silane三甲基乙炔基硅四甲基乙二胺copper(l) chloride 作用下, 以 丙酮 为溶剂, 反应 45.0h, 以84%的产率得到4-[3,5-Bis[2-[2,5-didecoxy-4-[2-[2,5-didecoxy-4-[2-tri(propan-2-yl)silylethynyl]phenyl]ethynyl]phenyl]ethynyl]phenyl]buta-1,3-diynyl-trimethylsilane
    参考文献:
    名称:
    Conjugated Oligoyne-Bridged [60]Fullerene Molecular Dumbbells: Syntheses and Thermal and Morphological Properties
    摘要:
    A series of linear and star-shaped pi-conjugated oligomer hybrids (2-5) composed of an oligoyne core, ranging from 1,3-butadiyne to 1,3,5.7,9,11-dodecahexayne, and fullerenyl end-capping groups has been synthesized and studied. The molecular structures of these fullerene-oligoyne hybrids were assembled through three key reactions. Pd-catalyzed cross-coupling, Cu-catalyzed oxidative homocoupling, and an in situ alkynylation reaction on [60]fullerene. The properties of these compound were investigated by UV-vis spectroscopy, differential scanning calorimetry (DSC), and atomic force microscopy (AFM) with the purpose of understanding the thermal reactivity arising from the oliogyne moieties as well as the morphological properties on surface. Our study shows that these fullerene-oliogyne hybrids tend to aggregate in different morphologies, including nanospheres, nanoflakes, and continuous thin films, while the morphological properties appear to be subject to the influence of molecular factors such as oligomer chain length, solubilizing alkylphenyl groups, and the thermal reactivity of the oligoyne unit. The correlation between molecular property and interfacial aggregation behavior evinced by these fullerene-oligoyne hybrids suggests a viable approach to exert bottom-up control over the structures and properties of fullerene based nanomaterials.
    DOI:
    10.1021/jo9021748
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文献信息

  • Conjugated Oligoyne-Bridged [60]Fullerene Molecular Dumbbells: Syntheses and Thermal and Morphological Properties
    作者:Ningzhang Zhou、Yuming Zhao
    DOI:10.1021/jo9021748
    日期:2010.3.5
    A series of linear and star-shaped pi-conjugated oligomer hybrids (2-5) composed of an oligoyne core, ranging from 1,3-butadiyne to 1,3,5.7,9,11-dodecahexayne, and fullerenyl end-capping groups has been synthesized and studied. The molecular structures of these fullerene-oligoyne hybrids were assembled through three key reactions. Pd-catalyzed cross-coupling, Cu-catalyzed oxidative homocoupling, and an in situ alkynylation reaction on [60]fullerene. The properties of these compound were investigated by UV-vis spectroscopy, differential scanning calorimetry (DSC), and atomic force microscopy (AFM) with the purpose of understanding the thermal reactivity arising from the oliogyne moieties as well as the morphological properties on surface. Our study shows that these fullerene-oliogyne hybrids tend to aggregate in different morphologies, including nanospheres, nanoflakes, and continuous thin films, while the morphological properties appear to be subject to the influence of molecular factors such as oligomer chain length, solubilizing alkylphenyl groups, and the thermal reactivity of the oligoyne unit. The correlation between molecular property and interfacial aggregation behavior evinced by these fullerene-oligoyne hybrids suggests a viable approach to exert bottom-up control over the structures and properties of fullerene based nanomaterials.
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