1,2-bis<6-(carboxyethyl)-2-methyl-1-benzothiophen-3-yl>hexafluorocyclopentene | 143619-58-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并噻吩类
• 英文名称: 1,2-bis<6-(carboxyethyl)-2-methyl-1-benzothiophen-3-yl>hexafluorocyclopentene
• 英文别名: 3-[3-[2-[6-(2-Carboxyethyl)-2-methyl-1-benzothiophen-3-yl]-3,3,4,4,5,5-hexafluorocyclopenten-1-yl]-2-methyl-1-benzothiophen-6-yl]propanoic acid；3-[3-[2-[6-(2-carboxyethyl)-2-methyl-1-benzothiophen-3-yl]-3,3,4,4,5,5-hexafluorocyclopenten-1-yl]-2-methyl-1-benzothiophen-6-yl]propanoic acid
• CAS: 143619-58-3
• 化学式: C₂₉H₂₂F₆O₄S₂
• 分子量: 612.614
• InChiKey: UEUQGPPVITUQCI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.1
• 重原子数：
  41
• 可旋转键数：
  8
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  131
• 氢给体数：
  2
• 氢受体数：
  12

反应信息

• 作为反应物：
  描述：

  1,2-bis<6-(carboxyethyl)-2-methyl-1-benzothiophen-3-yl>hexafluorocyclopentene 以 乙醇 、 环己烷 为溶剂， 生成
  参考文献：
  名称：

  二芳基乙烯的封闭光致变色

  摘要：

  我们通过将具有氢键能力的取代基引入 1,2-二芳基乙烯中来设计和合成化学门控分子。

  DOI：

  10.1021/ja00048a063
• 作为产物：
  描述：

  1,2-bis<6-<<(diazomethyl)carbonyl>methyl>-2-methylbenzothiophen-3-yl>hexafluorocyclopentene 在 硫酸 、 silver(l) oxide 作用下， 以 1,4-二氧六环 为溶剂， 反应 10.0h， 生成 1,2-bis<6-(carboxyethyl)-2-methyl-1-benzothiophen-3-yl>hexafluorocyclopentene
  参考文献：
  名称：

  Photochromic Diarylethenes with Intralocking Arms

  摘要：

  1,2-Bis(2-methylbenzo[b]thiophen-3-yl)perfluorocyclopentenes with carboxyalkyl or alkyl mercaptan groups at 6 and 6' positions of the benzothiophene rings were synthesized with the aim of controlling the photochromic reactivity by external stimulation, such as chemicals or heat treatment. 1,2-Diarylethenes with heterocyclic five-membered rings have two atropisomers, and the photochromic reactivity depends on the conformation. When the molecule was fixed in a parallel conformation with intramolecular hydrogen bonds or an intramolecular disulfide linkage, the photochromic reactivity was completely inhibited. The molecule again became photoactive when the intramolecular lock was unclasped by the addition of hydrogen bond breaking or reducing agents. The diarylethene with carboxyethyl groups showed a thermal reaction threshold in decalin. At temperatures below 50 degrees C the molecule was photochemically inactive, while the photochromic property was recovered upon heating above 100 degrees C, at which temperatures the intramolecular hydrogen bonds are broken.

  DOI：

  10.1021/ja00101a010

文献信息

• Blocked photochromism of diarylethenes
  作者：Masahiro Irie、Osamu Miyatake、Kingo Uchida

  DOI：10.1021/ja00048a063

  日期：1992.10

  We designed and synthesized chemical-gated molecules by introducing substitutents tha have hydrogen-bonding ability into 1,2-diarylethenes.

  我们通过将具有氢键能力的取代基引入 1,2-二芳基乙烯中来设计和合成化学门控分子。
• Photochromic Diarylethenes with Intralocking Arms
  作者：Masahiro Irie、Osamu Miyatake、Kingo Uchida、Takeshi Eriguchi

  DOI：10.1021/ja00101a010

  日期：1994.11

  1,2-Bis(2-methylbenzo[b]thiophen-3-yl)perfluorocyclopentenes with carboxyalkyl or alkyl mercaptan groups at 6 and 6' positions of the benzothiophene rings were synthesized with the aim of controlling the photochromic reactivity by external stimulation, such as chemicals or heat treatment. 1,2-Diarylethenes with heterocyclic five-membered rings have two atropisomers, and the photochromic reactivity depends on the conformation. When the molecule was fixed in a parallel conformation with intramolecular hydrogen bonds or an intramolecular disulfide linkage, the photochromic reactivity was completely inhibited. The molecule again became photoactive when the intramolecular lock was unclasped by the addition of hydrogen bond breaking or reducing agents. The diarylethene with carboxyethyl groups showed a thermal reaction threshold in decalin. At temperatures below 50 degrees C the molecule was photochemically inactive, while the photochromic property was recovered upon heating above 100 degrees C, at which temperatures the intramolecular hydrogen bonds are broken.