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tetra(3-thienyl)ethene | 1447111-33-2

中文名称
——
中文别名
——
英文名称
tetra(3-thienyl)ethene
英文别名
3-[1,2,2-Tri(thiophen-3-yl)ethenyl]thiophene;3-[1,2,2-tri(thiophen-3-yl)ethenyl]thiophene
tetra(3-thienyl)ethene化学式
CAS
1447111-33-2
化学式
C18H12S4
mdl
——
分子量
356.557
InChiKey
NLLBUUUMDAXWMG-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:
    434.3±40.0 °C(Predicted)
  • 密度:
    1.353±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.7
  • 重原子数:
    22
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    113
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    tetra(3-thienyl)ethene 在 iron(III) chloride 作用下, 以 二氯甲烷 为溶剂, 反应 1.0h, 以41%的产率得到5,6-di(3-thienyl)dithieno[2,3-a:3',2'-c]benzene
    参考文献:
    名称:
    Synthesis and basic properties of tetrathieno[2,3-a:3′,2′-c:2″,3″-f:3‴,2‴-h]naphthalene: a new π-conjugated system obtained by photoinduced electrocyclization–dehydrogenation reactions of tetra(3-thienyl)ethene
    摘要:
    method for the synthesis of tetrathieno[2,3-a:3',2'-c:2 '',3 ''-f:3''',2'''-h]naphthalene (3), utilizing photoinduced electrocyclization-dehydrogenation reactions of tetra(3-thienyl)ethene (1), was developed. Photoirradiation of a toluene or CHCl3 solution of 1, containing a small amount of I-2, leads to modestly efficient production of 3. In contrast to the UV-vis absorption property of the typical p-type organic transistor material pentacene, that of 3 does not experience a time-dependent change under aerated conditions, indicating that 3 has high stability against molecular oxygen. The results of X-ray crystallographic analysis demonstrate that 3 possesses a columnar crystalline structure in which molecules are aligned in a face-to-face manner with a high degree of the TE-TE overlap between adjacent molecules. This phenomenon should result in efficient charge-carrier transport properties of the crystalline form of this substance. C 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2013.05.090
  • 作为产物:
    描述:
    di(thiophen-3-yl)methanone吡啶四氯化钛 作用下, 以 四氢呋喃 为溶剂, 反应 1.5h, 以3.69 g的产率得到tetra(3-thienyl)ethene
    参考文献:
    名称:
    Synthesis and basic properties of tetrathieno[2,3-a:3′,2′-c:2″,3″-f:3‴,2‴-h]naphthalene: a new π-conjugated system obtained by photoinduced electrocyclization–dehydrogenation reactions of tetra(3-thienyl)ethene
    摘要:
    method for the synthesis of tetrathieno[2,3-a:3',2'-c:2 '',3 ''-f:3''',2'''-h]naphthalene (3), utilizing photoinduced electrocyclization-dehydrogenation reactions of tetra(3-thienyl)ethene (1), was developed. Photoirradiation of a toluene or CHCl3 solution of 1, containing a small amount of I-2, leads to modestly efficient production of 3. In contrast to the UV-vis absorption property of the typical p-type organic transistor material pentacene, that of 3 does not experience a time-dependent change under aerated conditions, indicating that 3 has high stability against molecular oxygen. The results of X-ray crystallographic analysis demonstrate that 3 possesses a columnar crystalline structure in which molecules are aligned in a face-to-face manner with a high degree of the TE-TE overlap between adjacent molecules. This phenomenon should result in efficient charge-carrier transport properties of the crystalline form of this substance. C 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2013.05.090
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