3-(2-(2,5-dimethylthiophen-3-yl)cyclopent-1-enyl)-2-methylbenzo[b]thiophene | 1312292-03-7

• 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: 3-(2-(2,5-dimethylthiophen-3-yl)cyclopent-1-enyl)-2-methylbenzo[b]thiophene
• 英文别名: 3-[2-(2,5-Dimethylthiophen-3-yl)cyclopenten-1-yl]-2-methyl-1-benzothiophene
• CAS: 1312292-03-7
• 化学式: C₂₀H₂₀S₂
• 分子量: 324.511
• InChiKey: NKTUFOYVSXJVRN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.2
• 重原子数：
  22
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  56.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  3-(2-(2,5-dimethylthiophen-3-yl)cyclopent-1-enyl)-2-methylbenzo[b]thiophene 以 乙腈 为溶剂， 生成
  参考文献：
  名称：

  Synthesis and Characterization of Nonsymmetric Cyclopentene-Based Dithienylethenes

  摘要：

  Nonsymmetric cyclopentene-based dithienylethenes, containing both thienyl and benzothienyl units, have been synthesized for the first time, employing intramolecular McMurry reaction as a key transformation to target compounds 10 and 16. Photochromic properties of these compounds were examined in toluene and acetonitrile solutions, PMMA layers, solid films, and crystal phase. To explain an unprecedented single-crystalline photochromism phenomena of 10, X-ray crystallographic analysis was performed, revealing a significant influence of strong S center dot center dot center dot S interatomic interactions on the intramolecular distance between two photochemical reaction centers in the molecule. Compound 16 could be further synthetically modified in a step-by-step manner, thus serving as potential key intermediate to various complex bifunctional photochromic molecules.

  DOI：

  10.1021/jo201966g
• 作为产物：
  描述：

  以 乙腈 为溶剂， 生成 3-(2-(2,5-dimethylthiophen-3-yl)cyclopent-1-enyl)-2-methylbenzo[b]thiophene
  参考文献：
  名称：

  Synthesis and Characterization of Nonsymmetric Cyclopentene-Based Dithienylethenes

  摘要：

  Nonsymmetric cyclopentene-based dithienylethenes, containing both thienyl and benzothienyl units, have been synthesized for the first time, employing intramolecular McMurry reaction as a key transformation to target compounds 10 and 16. Photochromic properties of these compounds were examined in toluene and acetonitrile solutions, PMMA layers, solid films, and crystal phase. To explain an unprecedented single-crystalline photochromism phenomena of 10, X-ray crystallographic analysis was performed, revealing a significant influence of strong S center dot center dot center dot S interatomic interactions on the intramolecular distance between two photochemical reaction centers in the molecule. Compound 16 could be further synthetically modified in a step-by-step manner, thus serving as potential key intermediate to various complex bifunctional photochromic molecules.

  DOI：

  10.1021/jo201966g

文献信息

• Synthesis and Characterization of Nonsymmetric Cyclopentene-Based Dithienylethenes
  作者：Vasily A. Migulin、Michael M. Krayushkin、Valery A. Barachevsky、Olga I. Kobeleva、Tatyana M. Valova、Konstantin A. Lyssenko

  DOI：10.1021/jo201966g

  日期：2012.1.6

  Nonsymmetric cyclopentene-based dithienylethenes, containing both thienyl and benzothienyl units, have been synthesized for the first time, employing intramolecular McMurry reaction as a key transformation to target compounds 10 and 16. Photochromic properties of these compounds were examined in toluene and acetonitrile solutions, PMMA layers, solid films, and crystal phase. To explain an unprecedented single-crystalline photochromism phenomena of 10, X-ray crystallographic analysis was performed, revealing a significant influence of strong S center dot center dot center dot S interatomic interactions on the intramolecular distance between two photochemical reaction centers in the molecule. Compound 16 could be further synthetically modified in a step-by-step manner, thus serving as potential key intermediate to various complex bifunctional photochromic molecules.