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C60(CH2SiMe2C6H13)H | 1082487-38-4

中文名称
——
中文别名
——
英文名称
C60(CH2SiMe2C6H13)H
英文别名
1-(Hexyldimethylsilylmethyl)-1,9-dihydro(C60-Ih)[5,6]fullerene
C60(CH2SiMe2C6H13)H化学式
CAS
1082487-38-4
化学式
C69H22Si
mdl
——
分子量
879.019
InChiKey
CVOVGWWYRCXEDB-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):
    20.43
  • 重原子数:
    70.0
  • 可旋转键数:
    7.0
  • 环数:
    32.0
  • sp3杂化的碳原子比例:
    0.16
  • 拓扑面积:
    0.0
  • 氢给体数:
    0.0
  • 氢受体数:
    0.0

反应信息

  • 作为反应物:
    描述:
    C60(CH2SiMe2C6H13)Hpotassium tert-butylate 作用下, 以 四氢呋喃邻二氯苯 为溶剂, 反应 0.27h, 生成
    参考文献:
    名称:
    Regioselective [2 + 2] Cycloaddition of a Fullerene Dimer with an Alkyne Triggered by Thermolysis of an Interfullerene C–C Bond
    摘要:
    Heating of a singly bonded fullerene dimer in the presence of an alkyne forms a cyclobutene structure on only one of the two fullerene moieties, through a stereo- and regioselective [2 + 2] cycloaddition. Experimental and theoretical data suggest that the reaction is triggered by cleavage of the interfullerene C-C bond and formation of a monomeric fullerene radical.
    DOI:
    10.1021/ol400713t
  • 作为产物:
    描述:
    (C6H13)Me2SiCH2MgCl足球烯N,N-二甲基甲酰胺 作用下, 以 四氢呋喃邻二氯苯 为溶剂, 反应 0.08h, 以83%的产率得到C60(CH2SiMe2C6H13)H
    参考文献:
    名称:
    Regioselective Synthesis of 1,4-Di(organo)[60]fullerenes through DMF-assisted Monoaddition of Silylmethyl Grignard Reagents and Subsequent Alkylation Reaction
    摘要:
    Monoaddition of Grignard reagents, in particular tri(organo)silylmethyl magnesium chlorides, to [60]fullerene took place smoothly in the presence of dimethylformamideto produce (organo)(hydro)[60]fullerenes, (C60RH)-H-1, in good yield (up to 93% isolated yield). The hydrofullerene was then deprotonated to generate the corresponding anion, C60R-, which was then alkylated to obtain 58 pi-electron di(organo)[60]fullerenes, (C60RR2)-R-1, in good to high yield (up to 93% overall yield). The two-step methodology provides a wide variety of 1,4-di(organo)[60] fullerenes bearing the same or different organic addends on the [60] fullerene core. By changing the addends, one can control the chemical and physical properties of the compounds at the molecular and bulk levels.
    DOI:
    10.1021/ja8041299
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