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3-tridecanoxythiophene | 120621-20-7

中文名称
——
中文别名
——
英文名称
3-tridecanoxythiophene
英文别名
3-Tridecoxythiophene
3-tridecanoxythiophene化学式
CAS
120621-20-7
化学式
C17H30OS
mdl
——
分子量
282.491
InChiKey
RWXNXMUNPKDNLA-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):
    7.7
  • 重原子数:
    19
  • 可旋转键数:
    13
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.76
  • 拓扑面积:
    37.5
  • 氢给体数:
    0
  • 氢受体数:
    2

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:
    3-tridecanoxythiopheneN-溴代丁二酰亚胺(NBS)溶剂黄146 作用下, 以 氯仿 为溶剂, 反应 21.5h, 以87%的产率得到2-bromo-3-tridecanoxythiophene
    参考文献:
    名称:
    Synthesis, characterization, and field-effect transistor performance of poly[2,6-bis(3-tridecanoxythiophen-2-yl)benzo[1,2-b;4,5-b′]dithiophene]
    摘要:
    AbstractA new copolymer of benzo[1,2‐b:4,5‐b′]dithiophene and 3,3′‐bis(tridecanoxy)‐5,5′‐bithiophene was synthesized through Stille copolymerization. The bis‐(3‐alkoxythiophene) monomer was synthesized through a silver fluoride mediated, palladium‐catalyzed cross‐coupling, in which bromide functional groups were preserved instead of consumed. The copolymer has been characterized and applied in field‐effect transistors, giving a hole mobility of 2 × 10−3 cm2/Vs and an on/off ratio >106, with negligible hysteresis, on standard silicon substrates. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1973–1978, 2010
    DOI:
    10.1002/pola.23964
  • 作为产物:
    描述:
    3-甲氧基噻吩十三烷醇碳酸氢钠 作用下, 以 甲苯 为溶剂, 反应 20.0h, 以89%的产率得到3-tridecanoxythiophene
    参考文献:
    名称:
    Synthesis, characterization, and field-effect transistor performance of poly[2,6-bis(3-tridecanoxythiophen-2-yl)benzo[1,2-b;4,5-b′]dithiophene]
    摘要:
    AbstractA new copolymer of benzo[1,2‐b:4,5‐b′]dithiophene and 3,3′‐bis(tridecanoxy)‐5,5′‐bithiophene was synthesized through Stille copolymerization. The bis‐(3‐alkoxythiophene) monomer was synthesized through a silver fluoride mediated, palladium‐catalyzed cross‐coupling, in which bromide functional groups were preserved instead of consumed. The copolymer has been characterized and applied in field‐effect transistors, giving a hole mobility of 2 × 10−3 cm2/Vs and an on/off ratio >106, with negligible hysteresis, on standard silicon substrates. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1973–1978, 2010
    DOI:
    10.1002/pola.23964
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文献信息

  • Synthesis, characterization, and field-effect transistor performance of poly[2,6-bis(3-tridecanoxythiophen-2-yl)benzo[1,2-b;4,5-b′]dithiophene]
    作者:Mark A. M. Leenen、Tim Meyer、Fabio Cucinotta、Heiko Thiem、Ralf Anselmann、Luisa De Cola
    DOI:10.1002/pola.23964
    日期:2010.5.1
    AbstractA new copolymer of benzo[1,2‐b:4,5‐b′]dithiophene and 3,3′‐bis(tridecanoxy)‐5,5′‐bithiophene was synthesized through Stille copolymerization. The bis‐(3‐alkoxythiophene) monomer was synthesized through a silver fluoride mediated, palladium‐catalyzed cross‐coupling, in which bromide functional groups were preserved instead of consumed. The copolymer has been characterized and applied in field‐effect transistors, giving a hole mobility of 2 × 10−3 cm2/Vs and an on/off ratio >106, with negligible hysteresis, on standard silicon substrates. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1973–1978, 2010
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