4,5-bis(methylthio)-4',5'-bis(2-thienylethynyl)tetrathiafulvalene | 1235983-12-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 杂芳族化合物
• 英文名称: 4,5-bis(methylthio)-4',5'-bis(2-thienylethynyl)tetrathiafulvalene
• 英文别名: 2-[4,5-Bis(methylsulfanyl)-1,3-dithiol-2-ylidene]-4,5-bis(2-thiophen-2-ylethynyl)-1,3-dithiole；2-[4,5-bis(methylsulfanyl)-1,3-dithiol-2-ylidene]-4,5-bis(2-thiophen-2-ylethynyl)-1,3-dithiole
• CAS: 1235983-12-6
• 化学式: C₂₀H₁₂S₈
• 分子量: 508.843
• InChiKey: VQJDWIVRZHMWJA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.5
• 重原子数：
  28
• 可旋转键数：
  6
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.1
• 拓扑面积：
  208
• 氢给体数：
  0
• 氢受体数：
  8

反应信息

• 作为产物：
  描述：

  2-乙炔噻吩 、 4,5-diiodo-4',5'-bis(methylthio)tetrathiafulvalene 在 copper(l) iodide 、 四(三苯基膦)钯 、 三乙胺 作用下， 以 苯 为溶剂， 反应 4.0h， 以72%的产率得到4,5-bis(methylthio)-4',5'-bis(2-thienylethynyl)tetrathiafulvalene
  参考文献：
  名称：

  Synthesis and Properties of Thienylene-Ethynylene-Tetrathiafulvalene Oligomers

  摘要：

  A series of thienylene-ethynylene-tetrathiafulvalene oligomers 1-6 have been synthesized by the Sonogashira reaction of iodo-tetrathiafulvalene derivatives with thienylethynes. The X-ray structure of 4,5-bis(2-thienylethynyl)tetrathiafulvalene (1b) revealed a planar structure of the molecule. The electronic spectra of neutral oligomers 1-6 suggest a partial intramolecular charge transfer between the TTF and thienylethyne units. The cyclic voltammetric measurements of 1-4 showed multi-redox processes.

  DOI：

  10.1080/10426501003773381

文献信息

• Synthesis and Properties of Thienylene-Ethynylene-Tetrathiafulvalene Oligomers
  作者：Masashi Hasegawa、Kenji Hara、Ken-ichi Tokuyama、Masahiko Iyoda

  DOI：10.1080/10426501003773381

  日期：2010.5.27

  A series of thienylene-ethynylene-tetrathiafulvalene oligomers 1-6 have been synthesized by the Sonogashira reaction of iodo-tetrathiafulvalene derivatives with thienylethynes. The X-ray structure of 4,5-bis(2-thienylethynyl)tetrathiafulvalene (1b) revealed a planar structure of the molecule. The electronic spectra of neutral oligomers 1-6 suggest a partial intramolecular charge transfer between the TTF and thienylethyne units. The cyclic voltammetric measurements of 1-4 showed multi-redox processes.