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4-(2-(5-bromo-2,2'-bithiophen-5'-yl)ethynyl)benzaldehyde | 1374843-67-0

中文名称
——
中文别名
——
英文名称
4-(2-(5-bromo-2,2'-bithiophen-5'-yl)ethynyl)benzaldehyde
英文别名
——
4-(2-(5-bromo-2,2'-bithiophen-5'-yl)ethynyl)benzaldehyde化学式
CAS
1374843-67-0
化学式
C17H9BrOS2
mdl
——
分子量
373.294
InChiKey
CQCKJVBWBBMJJD-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):
    5.45
  • 重原子数:
    21.0
  • 可旋转键数:
    2.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    17.07
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

上下游信息

  • 下游产品
    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:
    4-(2-(5-bromo-2,2'-bithiophen-5'-yl)ethynyl)benzaldehyde3,6-di-tert-butyl-9-(4-ethynylphenyl)-9H-carbazole 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodideN,N-二异丙基乙胺三苯基膦 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 14.0h, 以82%的产率得到4-(2-(5-(2-(4-(3,6-di-tert-butyl-9H-carbazolyl)phenyl)ethynyl)-2,2'-bithiophen-5'-yl)ethynyl)benzaldehyde
    参考文献:
    名称:
    Carbazole donor and carbazole or bithiophene bridged sensitizers for dye-sensitized solar cells
    摘要:
    Three metal-free organic sensitizers consisting of carbazole as an electron donor, carbazole or bithiophene as the linker and cyanoacrylic acid as the electron acceptor and anchoring groups were designed and synthesized for use in dye-sensitized solar cells (DSSCs). The sensitizers were characterized by H-1 and C-13 NMR, MALDI-TOF (or HRMS), UV-Vis, photoluminescence, and electrochemistry. The HOMO and LUMO electron distributions of the sensitizers were calculated using density functional theory on a B3LYP level for geometry optimization. The photovoltaic performance of the sensitizers in operational liquid junction-based DSSCs under AM 1.5 G one-sun excitation (100 mW/cm(2)) indicate that the sensitizers are promising candidates for use in DSSCs. Sensitizers 1 and 2 produce a power conversion efficiency of 2.70% with a maximum IPCE of 75% at 450 nm, while sensitizer 3 has a power conversion efficiency of 2.23% with a maximum IPCE of 66% at 440 nm. The sensitizers thus exhibit excellent photon-to-current conversion efficiencies in the blue region of the spectrum and serve as candidates for further strategic optimization in tandem cells. (C) 2011 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jphotochem.2011.08.001
  • 作为产物:
    描述:
    5,5'-二溴-2,2'-联噻吩4-乙炔基苯甲醛 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodideN,N-二异丙基乙胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以65%的产率得到4-(2-(5-bromo-2,2'-bithiophen-5'-yl)ethynyl)benzaldehyde
    参考文献:
    名称:
    Carbazole donor and carbazole or bithiophene bridged sensitizers for dye-sensitized solar cells
    摘要:
    Three metal-free organic sensitizers consisting of carbazole as an electron donor, carbazole or bithiophene as the linker and cyanoacrylic acid as the electron acceptor and anchoring groups were designed and synthesized for use in dye-sensitized solar cells (DSSCs). The sensitizers were characterized by H-1 and C-13 NMR, MALDI-TOF (or HRMS), UV-Vis, photoluminescence, and electrochemistry. The HOMO and LUMO electron distributions of the sensitizers were calculated using density functional theory on a B3LYP level for geometry optimization. The photovoltaic performance of the sensitizers in operational liquid junction-based DSSCs under AM 1.5 G one-sun excitation (100 mW/cm(2)) indicate that the sensitizers are promising candidates for use in DSSCs. Sensitizers 1 and 2 produce a power conversion efficiency of 2.70% with a maximum IPCE of 75% at 450 nm, while sensitizer 3 has a power conversion efficiency of 2.23% with a maximum IPCE of 66% at 440 nm. The sensitizers thus exhibit excellent photon-to-current conversion efficiencies in the blue region of the spectrum and serve as candidates for further strategic optimization in tandem cells. (C) 2011 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jphotochem.2011.08.001
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同类化合物

锡烷,1,1'-(3,3'-二烷基[2,2'-二噻吩]-5,5'-二基)双[1,1,1-三甲基- 试剂5,10-Bis((5-octylthiophen-2-yl)dithieno[2,3-d:2',3'-d']benzo[1,2-b:4,5-b']dithiophene-2,7-diyl)bis(trimethylstannane) 试剂2,2'-Thieno[3,2-b]thiophene-2,5-diylbis-3-thiophenecarboxylicacid 试剂1,1'-[4,8-Bis[5-(dodecylthio)-2-thienyl]benzo[1,2-b:4,5-b']dithiophene-2,6-diyl]bis[1,1,1-trimethylstannane] 苯并[b]噻吩,3-(2-噻嗯基)- 聚(3-己基噻吩-2,5-二基)(区域规则) 甲基[2,3'-联噻吩]-5-羧酸甲酯 牛蒡子醇 B 噻吩并[3,4-B]吡嗪,5,7-二-2-噻吩- 噻吩[3,4-B]吡嗪,5,7-双(5-溴-2-噻吩)- 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) IN1538,4,6-双(4-癸基噻吩基)-噻吩并[3,4-C][1,2,5]噻二唑(S) C-[2,2-二硫代苯-5-基甲基]胺 6,6,12,12-四(4-己基苯基)-6,12-二氢二噻吩并[2,3-D:2',3'-D']-S-苯并二茚并[1,2-B:5,6-B']二噻吩-2,8-双三甲基锡 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