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2-(4-己基苯基)-5-[5-(4-己基苯基)噻吩-2-基]噻吩 | 583884-12-2

中文名称
2-(4-己基苯基)-5-[5-(4-己基苯基)噻吩-2-基]噻吩
中文别名
——
英文名称
5,5'-bis(4-n-hexylphenyl)-2,2'-bithiophene
英文别名
2,2'-Bithiophene, 5,5'-bis(4-hexylphenyl)-;2-(4-hexylphenyl)-5-[5-(4-hexylphenyl)thiophen-2-yl]thiophene
2-(4-己基苯基)-5-[5-(4-己基苯基)噻吩-2-基]噻吩化学式
CAS
583884-12-2
化学式
C32H38S2
mdl
——
分子量
486.786
InChiKey
KVIKDTOMNCCKCN-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):
    12.2
  • 重原子数:
    34
  • 可旋转键数:
    13
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    56.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    1-(4-溴苯基)己烷2,2'-联二噻吩 在 palladium diacetate 、 potassium carbonate 、 tricyclohexylphosphine tetrafluoroborate 、 三甲基乙酸 作用下, 以 N,N-二甲基乙酰胺 为溶剂, 反应 16.0h, 以87%的产率得到2-(4-己基苯基)-5-[5-(4-己基苯基)噻吩-2-基]噻吩
    参考文献:
    名称:
    Direct Arylation as a Synthetic Tool for the Synthesis of Thiophene-Based Organic Electronic Materials
    摘要:
    The efficient synthesis of thiophene based organic electronic materials can be carried out in high yields using simple starting materials by employing palladium-catalyzed direct arylation. The direct arylation method was applied to the (formal) synthesis of ten molecules that have exhibited promise for applications as optoelectronic materials. The syntheses feature the following advantages over traditional cross-coupling techniques: (1) higher yields, (2) fewer synthetic operations, (3) lower catalyst loadings, and (4) does not employ organometallic intermediates. The advantages of direct arylation make it an ideal strategy for the synthesis of thiophene containing organic electronic materials.
    DOI:
    10.1021/cm103483q
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文献信息

  • Easily Processable Phenylene−Thiophene-Based Organic Field-Effect Transistors and Solution-Fabricated Nonvolatile Transistor Memory Elements
    作者:Melissa Mushrush、Antonio Facchetti、Michael Lefenfeld、Howard E. Katz、Tobin J. Marks
    DOI:10.1021/ja035143a
    日期:2003.8.1
    oligomers is reported; 2,5-bis(4-n-hexylphenyl)thiophene (dH-PTP, 1), 5,5'-bis(4-n-hexylphenyl)-2,2'-bithiophene (dH-PTTP, 2), 5,5' '-bis(4-n-hexylphenyl)-2,2':5',2' '-terthiophene (dH-PT(3)P, 3), 5,5' "-bis(4-n-hexylphenyl)-2,2':5',2' ':5' ',2' "-quaterthiophene (dH-PT(4)P, 4), 1,4-bis[5-(4-n-hexylphenyl)-2-thienyl]benzene (dH-PTPTP, 5), and 2,5-bis[4(4'-n-hexylphenyl)phenyl]thiophene (dH-PPTPP, 6) were
    报道了一系列新的混合苯-噻吩低聚物的合成;2,5-双(4-n-己基苯基)噻吩 (dH-PTP, 1), 5,5'-双(4-n-己基苯基)-2,2'-联噻吩 (dH-PTTP, 2), 5 ,5''-bis(4-n-hexylphenyl)-2,2':5',2''-三联噻吩(dH-PT(3)P, 3), 5,5'"-bis(4-n) -己基苯基)-2,2':5',2'':5'',2'"-季噻吩 (dH-PT(4)P, 4), 1,4-bis[5-(4-n-己基苯基)-2-噻吩基]苯 (dH-PTPTP, 5) 和 2,5-双[4(4'-n-己基苯基)苯基]噻吩 (dH-PPTPP, 6) 通过 (1)H NMR 表征、元素分析、紫外-可见光谱、差示扫描量热法和热重分析。真空蒸发和溶液流延薄膜的特点是 X 射线衍射和扫描电子显微镜。所有化合物在 Si/SiO(2) 和 ITO/上的蒸发(高达 0
  • Crosslinked polymeric dielectric materials and methods of manufacturing and use thereof
    申请人:Marks Tobin J.
    公开号:US20080161464A1
    公开(公告)日:2008-07-03
    Solution-processable dielectric materials are provided, along with precursor compositions and processes for preparing the same. Composites and electronic devices including the dielectric materials also are provided.
    提供可溶解处理的介电材料,以及制备这些材料的前体组成物和过程。还提供包括介电材料的复合材料和电子器件。
  • Crosslinked Polymeric Dielectric Materials And Electronic Devices Incorporating Same
    申请人:Marks Tobin J.
    公开号:US20110024729A1
    公开(公告)日:2011-02-03
    Solution-processable dielectric materials are provided, along with precursor compositions and processes for preparing the same. Composites and electronic devices including the dielectric materials also are provided.
    提供可溶解的介电材料,以及用于制备该材料的前体组合物和过程。还提供包括该介电材料的复合材料和电子器件。
  • BIOMETRIC SENSOR AND SENSOR PANEL
    申请人:Saito Tamio
    公开号:US20080054875A1
    公开(公告)日:2008-03-06
    A biometric sensor panel includes (a) a first flexible substrate, (b) a plurality of first electrodes formed on the first flexible substrate, the first electrodes being arranged in a first direction, (c) a semiconductor layer formed on the first electrodes, (d) a second flexible substrate, (e) a plurality of second electrodes formed on the second flexible substrate, the second electrodes being arranged in a second direction crossing the first direction, and (f) a pressure sensitive conductive layer formed on the second electrodes, wherein the first and second flexible substrates face each other such that the semiconductor layer is in contact with the pressure sensitive conductive layer.
  • BIOSENSOR SYSTEMS AND RELATED METHODS FOR DETECTING ANALYTES IN AQUEOUS AND BIOLOGICAL ENVIRONMENTS
    申请人:THE JOHNS HOPKINS UNIVERSITY
    公开号:US20140349005A1
    公开(公告)日:2014-11-27
    Disclosed herein are biosensor systems and related methods for detecting analytes in aqueous and biologic environments. A biosensor system for detecting binding of an analyte of interest may include a detector configured to detect a change in an electrical property on a surface thereof. The detector may be a FET. The system also may include a passive layer disposed on a top surface of the detector. Further, the system may include a hydrophobic layer disposed on the passive layer. The system also may include a receptor-attachment material configured for binding to an analyte. A receptor may bind to the analyte, and the receptor may be attached to the receptor-attachment material. The binding of the analyte to the receptor can cause the change of the electrical property at the surface. In response to the change for example, a current may change for indicating the binding of the analyte to the receptor.
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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