4-[5-[7-[4-[5-[2,5-Bis(2-ethylhexyl)-1-[5-[7-(7-methyl-2,1,3-benzothiadiazol-4-yl)-2,1,3-benzothiadiazol-4-yl]thiophen-2-yl]-3,6-dioxopyrrolo[3,4-c]pyrrol-4-yl]thiophen-2-yl]-2,1,3-benzothiadiazol-7-yl]-2,1,3-benzothiadiazol-4-yl]thiophen-2-yl]-1-(5-methylthiophen-2-yl)-2,5-dioctylpyrrolo[3,4-c]pyrrole-3,6-dione

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并噻二唑类
• 英文名称: 4-[5-[7-[4-[5-[2,5-Bis(2-ethylhexyl)-1-[5-[7-(7-methyl-2,1,3-benzothiadiazol-4-yl)-2,1,3-benzothiadiazol-4-yl]thiophen-2-yl]-3,6-dioxopyrrolo[3,4-c]pyrrol-4-yl]thiophen-2-yl]-2,1,3-benzothiadiazol-7-yl]-2,1,3-benzothiadiazol-4-yl]thiophen-2-yl]-1-(5-methylthiophen-2-yl)-2,5-dioctylpyrrolo[3,4-c]pyrrole-3,6-dione
• 英文别名: 4-[5-[7-[4-[5-[2,5-bis(2-ethylhexyl)-1-[5-[7-(7-methyl-2,1,3-benzothiadiazol-4-yl)-2,1,3-benzothiadiazol-4-yl]thiophen-2-yl]-3,6-dioxopyrrolo[3,4-c]pyrrol-4-yl]thiophen-2-yl]-2,1,3-benzothiadiazol-7-yl]-2,1,3-benzothiadiazol-4-yl]thiophen-2-yl]-1-(5-methylthiophen-2-yl)-2,5-dioctylpyrrolo[3,4-c]pyrrole-3,6-dione
• 化学式: C₈₆H₉₀N₁₂O₄S₈
• 分子量: 1612.2
• InChiKey: IDMMTPBDGIOFLU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  22.9
• 重原子数：
  110
• 可旋转键数：
  35
• 环数：
  16.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  410
• 氢给体数：
  0
• 氢受体数：
  20

文献信息

• PHOTOELECTRIC CONVERSION ELEMENT AND MANUFACTURING METHOD THEREOF
  申请人：ASAHI GLASS COMPANY, LIMITED

  公开号：US20140130871A1

  公开（公告）日：2014-05-15

  There are provided a photoelectric conversion element with high photoelectric conversion efficiency, whose light absorption efficiency, charge separation efficiency, and charge transport efficiency are at high level, and a method for efficiently manufacturing the photoelectric conversion element. A photoelectric conversion element has an anode, a cathode opposed to the anode, and an organic film disposed between the anode and the cathode and containing a liquid-crystalline conjugated block polymer. A method of manufacturing the above mentioned photoelectric conversion element has the step of, (1) preparing an organic film forming composition containing the liquid-crystalline conjugated block polymer; (2) forming the one electrode and a coating film using the composition on it; (3) heat treating the coating film within a temperature range in a liquid-crystalline state so as to obtain an organic film; and (4) forming the other electrode which is not formed in the step (2) above the organic film.