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1,3-Bis[4-hexyl-5-(4,6-dioxo-5,5-difluoro-5,6-dihydro-4H-cyclopenta[b]thiophene-2-yl)-2-thienyl]-5,5-difluoro-4H-cyclopenta[c]thiophene-4,6(5H)-dione | 1160067-00-4

中文名称
——
中文别名
——
英文名称
1,3-Bis[4-hexyl-5-(4,6-dioxo-5,5-difluoro-5,6-dihydro-4H-cyclopenta[b]thiophene-2-yl)-2-thienyl]-5,5-difluoro-4H-cyclopenta[c]thiophene-4,6(5H)-dione
英文别名
1,3-bis[5-(5,5-difluoro-4,6-dioxocyclopenta[b]thiophen-2-yl)-4-hexylthiophen-2-yl]-5,5-difluorocyclopenta[c]thiophene-4,6-dione
1,3-Bis[4-hexyl-5-(4,6-dioxo-5,5-difluoro-5,6-dihydro-4H-cyclopenta[b]thiophene-2-yl)-2-thienyl]-5,5-difluoro-4H-cyclopenta[c]thiophene-4,6(5H)-dione化学式
CAS
1160067-00-4
化学式
C41H30F6O6S5
mdl
——
分子量
893.006
InChiKey
IQKXFVOSPJBKOI-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):
    14.3
  • 重原子数:
    58
  • 可旋转键数:
    14
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.37
  • 拓扑面积:
    244
  • 氢给体数:
    0
  • 氢受体数:
    17

反应信息

  • 作为产物:
    描述:
    硫酸 作用下, 以 四氢呋喃 为溶剂, 反应 12.0h, 以113 mg的产率得到1,3-Bis[4-hexyl-5-(4,6-dioxo-5,5-difluoro-5,6-dihydro-4H-cyclopenta[b]thiophene-2-yl)-2-thienyl]-5,5-difluoro-4H-cyclopenta[c]thiophene-4,6(5H)-dione
    参考文献:
    名称:
    Electronegative Oligothiophenes Having Difluorodioxocyclopentene-annelated Thiophenes as Solution-processable n-Type OFET Materials
    摘要:
    我们合成了含有二氟二氧环戊烯-沟道化噻吩的可溶液加工的负电性低聚噻吩。通过吸收光谱和电化学测量研究了这些低聚物的电子特性。通过旋涂法制造的薄膜显示出典型的 n 沟道 OFET 行为。
    DOI:
    10.1246/cl.2009.460
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文献信息

  • EP2223918
    申请人:——
    公开号:——
    公开(公告)日:——
  • CONJUGATED COMPOUND, NITROGENATED CONDENSED-RING COMPOUND, NITROGENATED CONDENSED-RING POLYMER, ORGANIC THIN FILM, AND ORGANIC THIN FILM ELEMENT
    申请人:Aso Yoshio
    公开号:US20100301314A1
    公开(公告)日:2010-12-02
    According to the first invention group there are provided conjugated compounds having two or more groups represented by the following formula (I) or the following formula (II): wherein one of Ar and Ar′ represents a C6 or greater divalent aromatic hydrocarbon group and the other represents a C4 or greater divalent heterocyclic group, wherein the groups each may have a substituent, with the proviso that the groups as a whole contain no fluorine atoms, R 1 and R 2 each independently represent a hydrogen atom, a halogen atom or a monovalent group, and Ar″ represents a trivalent aromatic hydrocarbon or trivalent heterocyclic group; when the conjugated compound has two or more groups represented by formula (I), the portion excluding these groups contain no fluorine atoms. According to the second group of the present invention there are provided nitrogen-containing fused-ring compounds represented by the following formula (α-I): in formula (α-I), R 21 and R 22 each independently represent a hydrogen atom, a halogen atom or an optionally substituted monovalent group, and Z 21 and Z 22 each independently represent any one of the groups represented by the following formulas (α-i)-(α-ix); wherein R 23 , R 24 , R 25 and R 26 each independently represent a hydrogen atom, a halogen atom or a monovalent group, and R 23 and R 24 may bond together to form a ring, the left side and the right side of the group represented by formula (α-viii) may be interchanged.
  • US8378338B2
    申请人:——
    公开号:US8378338B2
    公开(公告)日:2013-02-19
  • Electronegative Oligothiophenes Having Difluorodioxocyclopentene-annelated Thiophenes as Solution-processable n-Type OFET Materials
    作者:Yutaka Ie、Makoto Okabe、Yoshikazu Umemoto、Hirokazu Tada、Yoshio Aso
    DOI:10.1246/cl.2009.460
    日期:2009.5.5
    Solution-processable electronegative oligothiophenes bearing difluorodioxocyclopentene-annelated thiophenes have been synthesized. The electronic properties of the oligomers were investigated by absorption spectroscopy and electrochemical measurements. Their films fabricated by spin-coating showed typical n-channel OFET behavior.
    我们合成了含有二氟二氧环戊烯-沟道化噻吩的可溶液加工的负电性低聚噻吩。通过吸收光谱和电化学测量研究了这些低聚物的电子特性。通过旋涂法制造的薄膜显示出典型的 n 沟道 OFET 行为。
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同类化合物

试剂2,2'-Thieno[3,2-b]thiophene-2,5-diylbis-3-thiophenecarboxylicacid 苯并[b]噻吩,3-(2-噻嗯基)- 甲基[2,3'-联噻吩]-5-羧酸甲酯 牛蒡子醇 B 十四氟-Alpha-六噻吩 三丁基(5''-己基-[2,2':5',2''-三联噻吩]-5-基)锡 α-四联噻吩 α-六噻吩 α-五联噻吩 α-七噻吩 α,ω-二己基四噻吩 5,5′-双(3-己基-2-噻吩基)-2,2′-联噻吩 α,ω-二己基六联噻吩 Α-八噻吩 alpha-三联噻吩甲醇 alpha-三联噻吩 [3,3-Bi噻吩]-2,2-二羧醛 [2,2’]-双噻吩-5,5‘-二甲醛 [2,2':5',2''-三联噻吩]-5,5''-二基双[三甲基硅烷] [2,2'-联噻吩]-5-甲醇,5'-(1-丙炔-1-基)- [2,2'-联噻吩]-5-甲酸甲酯 [2,2'-联噻吩]-5-乙酸,a-羟基-5'-(1-炔丙基)-(9CI) C-[2,2-二硫代苯-5-基甲基]胺 5’-己基-2,2’-联噻吩-5-硼酸频哪醇酯 5-辛基-1,3-二(噻吩-2-基)-4H-噻吩并[3,4-c]吡咯-4,6(5H)-二酮 5-苯基-2,2'-联噻吩 5-溴5'-辛基-2,2'-联噻吩 5-溴-5′-己基-2,2′-联噻吩 5-溴-5'-甲酰基-2,2':5'2'-三噻吩 5-溴-3,3'-二己基-2,2'-联噻吩 5-溴-3'-癸基-2,2':5',2''-三联噻吩 5-溴-2,2-双噻吩 5-溴-2,2'-联噻吩-5'-甲醛 5-氯-5'-苯基-2,2'-联噻吩 5-氯-2,2'-联噻吩 5-正辛基-2,2'-并噻吩 5-己基-5'-乙烯基-2,2'-联噻吩 5-己基-2,2-二噻吩 5-全氟己基-5'-溴-2,2'-二噻吩 5-全氟己基-2,2′-联噻吩 5-乙酰基-2,2-噻吩基 5-乙氧基-2,2'-联噻吩 5-丙酰基-2,2-二噻吩 5-{[[2,2'-联噻吩]-5-基}噻吩-2-腈 5-[5-(5-己基噻吩-2-基)噻吩-2-基]噻吩-2-羧酸 5-(羟甲基)-[2,2]-联噻吩 5-(噻吩-2-基)噻吩-2-甲腈 5-(5-甲酰基-3-己基噻吩-2-基)-4-己基噻吩-2-甲醛 5-(5-甲基噻吩-2-基)噻吩-2-甲醛 5-(5-噻吩-2-基噻吩-2-基)噻吩-2-羧酸 5-(5-乙炔基噻吩-2-基)噻吩-2-甲醛