2,5-bis(3-decylthiophen-2-yl)thiazolo[5,4-d]thiazole | 1024759-18-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 2,5-bis(3-decylthiophen-2-yl)thiazolo[5,4-d]thiazole
• 英文别名: 2,5-Bis(3-decylthiophen-2-yl)-[1,3]thiazolo[5,4-d][1,3]thiazole
• CAS: 1024759-18-9
• 化学式: C₃₂H₄₆N₂S₄
• 分子量: 586.995
• InChiKey: IXQFHDPFJGGURG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  15.1
• 重原子数：
  38
• 可旋转键数：
  20
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.62
• 拓扑面积：
  139
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  2,5-bis(3-decylthiophen-2-yl)thiazolo[5,4-d]thiazole 在 N-溴代丁二酰亚胺(NBS) 、 溶剂黄146 作用下， 以 氯仿 为溶剂， 生成 2,5-bis(5-bromo-3-decylthiophen-2-yl)thiazolo[5,4-d]thiazole
  参考文献：
  名称：

  具有萘[1,2- b：5,6 - b' ]二噻吩核的晶体D-π-A有机小分子，用于溶液处理的有机太阳能电池

  摘要：

  在这项工作中，我们设计并合成了一种新的含有萘并[1,2- b：5,6- b' ]二噻吩的扩大π共轭供体-受体（D-A）小分子NDT（TTz）2，用于溶液处理的有机光伏。通过顺序的Suzuki和Stille合成了NDT（TTz）2，其中NDT（TTz）2包含噻吩桥接的萘并[1,2- b：5,6 - b' ]二噻吩作为中心稠合核心，三苯胺侧翼噻吩噻唑并噻唑作为间隔基偶联反应。NDT（TTz）2的热，物理化学和电化学性质已通过差示扫描量热法，热重分析法，紫外可见光谱，光致发光光谱，X射线衍射和循环伏安法进行了评估。如光伏应用所希望的那样，NDT（TTz）2具有良好的溶解性，热稳定性和井井有条的π-π堆叠结晶性。NDT（TTz）2的光学带隙和HOMO能级分别确定为2.0 eV和-5.23 eV。除了研究有机薄膜晶体管外，还通过与PC 71一起制造溶液处理的体异质结太阳能电池，研究了NDT（TTz）

  DOI：

  10.1016/j.orgel.2012.09.019
• 作为产物：
  描述：

  Decylmagnesium bromide 在 N-溴代丁二酰亚胺(NBS) 、 正丁基锂 、 1,3-bis[(diphenylphosphino)propane]dichloronickel(II) 作用下， 以 乙醚 、 N,N-二甲基甲酰胺 为溶剂， 反应 18.0h， 生成 2,5-bis(3-decylthiophen-2-yl)thiazolo[5,4-d]thiazole
  参考文献：
  名称：

  Synthesis and characterization of triphenylamine flanked thiazole-based small molecules for high performance solution processed organic solar cells

  摘要：

  Two new small molecules, 5,5-bis(2-triphenylamino-3-decylthiophen-2-yl)-2,2-bithiazole (M1) and 2,5-bis(2-triphenylamino-3-decylthiophen-2-yl) thiazolo[5,4-d]thiazole (M2) based on an electron-donor triphenylamine unit and electron-acceptor thiophene-thiazolothiazole or thiophene-bithiazole units were synthesized by a palladium(0)-catalyzed Suzuki coupling reaction and examined as donor materials for application in organic solar cells. The small molecules had an absorption band in the range of 300-560 nm, with an optical band gap of 2.22 and 2.25 for M1 and M2, respectively. As determined by cyclic voltammetry, the highest occupied molecular orbital and lowest unoccupied molecular orbital energy levels of M1 were -5.27 eV and -3.05 eV, respectively, which were 0.05 eV and 0.02 eV greater than that of M2. Photovoltaic properties of the small molecules were investigated by constructing bulk-heterojunction organic solar cell (OSC) devices using M1 and M2 as donors and fullerene derivatives, 6,6-phenyl-C61-butyric acid methyl ester (PC61BM) and 6,6-phenyl-C71-butyric acid methyl ester (PC71BM) as acceptors with the device architecture ITO/PEDOT:PSS/M1 or M2:PCBM/LiF/Al. The effect of the small molecule/fullerene weight ratio, active layer thickness, and processing solvent were carefully investigated to improve the performance of the OSCs. Under AM 1.5 G 100 mW/cm(2) illumination, the optimized OSC device with M1 and PC71BM at a weight ratio of 1: 3 delivered a power conversion efficiency (PCE) of 1.30%, with a short circuit current of 4.63 mA/cm(2), an open circuit voltage of 0.97 V, and a fill factor of 0.29. In contrast, M2 produced a better performance under identical device conditions. A PCE as high as 2.39% was recorded, with a short circuit current of 6.49 mA/cm(2), an open circuit voltage of 0.94 V, and a fill factor of 0.39. (C) 2011 Elsevier B. V. All rights reserved.

  DOI：

  10.1016/j.orgel.2011.11.016

文献信息

• A crystalline D-π-A organic small molecule with naphtho[1,2-b:5,6-b′]dithiophene-core for solution processed organic solar cells
  作者：Pranabesh Dutta、Hanok Park、Woo-Hyoung Lee、In-Nam Kang、Soo-Hyoung Lee

  DOI：10.1016/j.orgel.2012.09.019

  日期：2012.12

  In this work, we have designed and synthesized a new naphtho[1,2-b:5,6-b′]dithiophene-containing enlarged π-conjugated donor–acceptor (D–A) small molecule, NDT(TTz)2, for use in solution-processed organic photovoltaics. NDT(TTz)2, which contains a thiophene-bridged naphtho[1,2-b:5,6-b′]dithiophene as the central fused core and triphenylamine-flanked thiophene thiazolothiazole as a spacer, was synthesized

  在这项工作中，我们设计并合成了一种新的含有萘并[1,2- b：5,6- b' ]二噻吩的扩大π共轭供体-受体（D-A）小分子NDT（TTz）2，用于溶液处理的有机光伏。通过顺序的Suzuki和Stille合成了NDT（TTz）2，其中NDT（TTz）2包含噻吩桥接的萘并[1,2- b：5,6 - b' ]二噻吩作为中心稠合核心，三苯胺侧翼噻吩噻唑并噻唑作为间隔基偶联反应。NDT（TTz）2的热，物理化学和电化学性质已通过差示扫描量热法，热重分析法，紫外可见光谱，光致发光光谱，X射线衍射和循环伏安法进行了评估。如光伏应用所希望的那样，NDT（TTz）2具有良好的溶解性，热稳定性和井井有条的π-π堆叠结晶性。NDT（TTz）2的光学带隙和HOMO能级分别确定为2.0 eV和-5.23 eV。除了研究有机薄膜晶体管外，还通过与PC 71一起制造溶液处理的体异质结太阳能电池，研究了NDT（TTz）
• Synthesis and characterization of triphenylamine flanked thiazole-based small molecules for high performance solution processed organic solar cells
  作者：Pranabesh Dutta、Wooseung Yang、Seung Hun Eom、Soo-Hyoung Lee

  DOI：10.1016/j.orgel.2011.11.016

  日期：2012.2

  Two new small molecules, 5,5-bis(2-triphenylamino-3-decylthiophen-2-yl)-2,2-bithiazole (M1) and 2,5-bis(2-triphenylamino-3-decylthiophen-2-yl) thiazolo[5,4-d]thiazole (M2) based on an electron-donor triphenylamine unit and electron-acceptor thiophene-thiazolothiazole or thiophene-bithiazole units were synthesized by a palladium(0)-catalyzed Suzuki coupling reaction and examined as donor materials for application in organic solar cells. The small molecules had an absorption band in the range of 300-560 nm, with an optical band gap of 2.22 and 2.25 for M1 and M2, respectively. As determined by cyclic voltammetry, the highest occupied molecular orbital and lowest unoccupied molecular orbital energy levels of M1 were -5.27 eV and -3.05 eV, respectively, which were 0.05 eV and 0.02 eV greater than that of M2. Photovoltaic properties of the small molecules were investigated by constructing bulk-heterojunction organic solar cell (OSC) devices using M1 and M2 as donors and fullerene derivatives, 6,6-phenyl-C61-butyric acid methyl ester (PC61BM) and 6,6-phenyl-C71-butyric acid methyl ester (PC71BM) as acceptors with the device architecture ITO/PEDOT:PSS/M1 or M2:PCBM/LiF/Al. The effect of the small molecule/fullerene weight ratio, active layer thickness, and processing solvent were carefully investigated to improve the performance of the OSCs. Under AM 1.5 G 100 mW/cm(2) illumination, the optimized OSC device with M1 and PC71BM at a weight ratio of 1: 3 delivered a power conversion efficiency (PCE) of 1.30%, with a short circuit current of 4.63 mA/cm(2), an open circuit voltage of 0.97 V, and a fill factor of 0.29. In contrast, M2 produced a better performance under identical device conditions. A PCE as high as 2.39% was recorded, with a short circuit current of 6.49 mA/cm(2), an open circuit voltage of 0.94 V, and a fill factor of 0.39. (C) 2011 Elsevier B. V. All rights reserved.