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N,N-diphenyl-3',4'-diethyl-2,2':5',2"-terthiophene-5-amine | 1210877-73-8

中文名称
——
中文别名
——
英文名称
N,N-diphenyl-3',4'-diethyl-2,2':5',2"-terthiophene-5-amine
英文别名
——
N,N-diphenyl-3',4'-diethyl-2,2':5',2"-terthiophene-5-amine化学式
CAS
1210877-73-8
化学式
C28H25NS3
mdl
——
分子量
471.711
InChiKey
WTHGQUFLSLQDFS-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

反应信息

  • 作为反应物:
    参考文献:
    名称:
    D-π-A Sensitizers for Dye-Sensitized Solar Cells: Linear vs Branched Oligothiophenes
    摘要:
    Two donor-pi-acceptor (D-pi-A) dyes, coded as L-3T-DPA 1 and B-5T-DPA 2, were synthesized for application in dye-sensitized solar cells. These D-pi-A sensitizers use diphenylamine donor, an oligothrophene as pi-bridge, and cyonoacrylic acid as an acceptor group that can be anchored to the surface of TiO2. While the two dyes comprise the same donor and acceptor units, the bridging oligothiophene is linear in one case and branched in the other case. Photophysical and electrochemical properties of the dyes were investigated by UV-vis spectrometry and cyclic voltammetry. The dyes were subsequently implemented as sensitizers in dye-sensitized solar cells. Photovoltaic devices with dye 1 showed a maximum monochromatic incident photon to current efficiency (IPCE) of 80% and an overall conversation efficiency of 6.8% under full sunlight (AM 1 5G, 100 mW cm(-2)) irradiation. The photovoltaic performance of branched dye 2 was lower because of less dye loading on the TiO2 surface. The dyes were also tested in ionic liquid and solid-state devices and showed good efficiencies. Long-term stability measurements were performed over 1000 h at full sunlight and at 60 degrees C in ionic liquid devices. Branched dye 2 thereby showed excellent stability retaining 96% of its initial efficiency, while linear dye 1 retained 73% after 1000 h of irradiation.
    DOI:
    10.1021/cm903542v
  • 作为产物:
    参考文献:
    名称:
    D-π-A Sensitizers for Dye-Sensitized Solar Cells: Linear vs Branched Oligothiophenes
    摘要:
    Two donor-pi-acceptor (D-pi-A) dyes, coded as L-3T-DPA 1 and B-5T-DPA 2, were synthesized for application in dye-sensitized solar cells. These D-pi-A sensitizers use diphenylamine donor, an oligothrophene as pi-bridge, and cyonoacrylic acid as an acceptor group that can be anchored to the surface of TiO2. While the two dyes comprise the same donor and acceptor units, the bridging oligothiophene is linear in one case and branched in the other case. Photophysical and electrochemical properties of the dyes were investigated by UV-vis spectrometry and cyclic voltammetry. The dyes were subsequently implemented as sensitizers in dye-sensitized solar cells. Photovoltaic devices with dye 1 showed a maximum monochromatic incident photon to current efficiency (IPCE) of 80% and an overall conversation efficiency of 6.8% under full sunlight (AM 1 5G, 100 mW cm(-2)) irradiation. The photovoltaic performance of branched dye 2 was lower because of less dye loading on the TiO2 surface. The dyes were also tested in ionic liquid and solid-state devices and showed good efficiencies. Long-term stability measurements were performed over 1000 h at full sunlight and at 60 degrees C in ionic liquid devices. Branched dye 2 thereby showed excellent stability retaining 96% of its initial efficiency, while linear dye 1 retained 73% after 1000 h of irradiation.
    DOI:
    10.1021/cm903542v
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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