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4,6-di-n-dodecylbenzo[2,1-b:3,4-b':5,6-c'']trithiophene | 1345692-43-4

中文名称
——
中文别名
——
英文名称
4,6-di-n-dodecylbenzo[2,1-b:3,4-b':5,6-c'']trithiophene
英文别名
8,10-Didodecyl-3,9,15-trithiatetracyclo[10.3.0.02,6.07,11]pentadeca-1(12),2(6),4,7,10,13-hexaene;8,10-didodecyl-3,9,15-trithiatetracyclo[10.3.0.02,6.07,11]pentadeca-1(12),2(6),4,7,10,13-hexaene
4,6-di-n-dodecylbenzo[2,1-b:3,4-b':5,6-c'']trithiophene化学式
CAS
1345692-43-4
化学式
C36H54S3
mdl
——
分子量
583.023
InChiKey
ISOCWOMQULAEQP-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):
    16.1
  • 重原子数:
    39
  • 可旋转键数:
    22
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    84.7
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    3,3'-bis(tetradec-1-ynyl)-2,2'-bithiophene 在 Wilkinson's catalyst 、 sulfur 作用下, 以 为溶剂, 反应 6.25h, 以23%的产率得到4,6-di-n-dodecylbenzo[2,1-b:3,4-b':5,6-c'']trithiophene
    参考文献:
    名称:
    Making Benzotrithiophene a Stronger Electron Donor
    摘要:
    A new member of the benzotrithiophene family, benzo[2,1-b:-3,44:5,6-c '']trithiophene (3a), and its alkyl substituted derivatives (3b-e) were synthesized and characterized. Their photophyscial, electrochemical, crystallographic, and self-assembly properties were described. Thin film structures varied widely with the exact nature of the alkyl substitution pattern, with decreasing self-assembly propensity with increasing alkyl chain length. The high HOMO levels and the coplanarity of these molecules show their potential as organic semiconductors and as donor components in donor-acceptor copolymers.
    DOI:
    10.1021/ol2025372
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文献信息

  • Making Benzotrithiophene a Stronger Electron Donor
    作者:Xin Guo、Suhao Wang、Volker Enkelmann、Martin Baumgarten、Klaus Müllen
    DOI:10.1021/ol2025372
    日期:2011.11.18
    A new member of the benzotrithiophene family, benzo[2,1-b:-3,44:5,6-c '']trithiophene (3a), and its alkyl substituted derivatives (3b-e) were synthesized and characterized. Their photophyscial, electrochemical, crystallographic, and self-assembly properties were described. Thin film structures varied widely with the exact nature of the alkyl substitution pattern, with decreasing self-assembly propensity with increasing alkyl chain length. The high HOMO levels and the coplanarity of these molecules show their potential as organic semiconductors and as donor components in donor-acceptor copolymers.
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