2,5-diiodo-3,4-dicyanothiophene | 189243-81-0

• 分子结构分类: 有机化合物 - 有机卤素化合物 - 芳基卤化物
• 英文名称: 2,5-diiodo-3,4-dicyanothiophene
• 英文别名: 2,5-Diiodothiophene-3,4-dicarbonitrile
• CAS: 189243-81-0
• 化学式: C₆I₂N₂S
• 分子量: 385.954
• InChiKey: PJRXAHMXLOXFBT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  11
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  75.8
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2,5-diiodo-3,4-dicyanothiophene 在 copper(l) iodide 、 四(三苯基膦)钯 、 对甲苯磺酸 、 二异丙胺 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 反应 12.0h， 生成 2,5-bis[(4-hydroxyphenyl)ethynyl]-3,4-dicyanothiophene
  参考文献：
  名称：

  The Interplay of Bent-Shape, Lateral Dipole and Chirality in Thiophene Based Di-, Tri-, and Tetracatenar Liquid Crystals

  摘要：

  A range of mesogenic molecules varying in both bend angle and strength of lateral dipole were synthesized, and their phase behavior was characterized by polarizing microscopy, thermal analysis, X-ray diffraction, and electrooptical measurements. We find the general destabilization of the liquid crystallinity caused by strong lateral dipolar groups and the bent molecular shape are off-set in mesomorphic tetracatenars, which display stable nematic, smectic, columnar, and cubic mesophases. The broad mesomorphism of the tetracatenars containing lateral dipoles and their incompatibility with chiral induction are explained by considering that loosely correlated dimers exist within the mesophases. Chiral mesophases of derivatives with strong lateral dipoles were achieved by attaching fewer or different side chains to each end of the mesogen.

  DOI：

  10.1021/ja0268027
• 作为产物：
  描述：

  3,4-二氰基噻吩 在 碘 、 lithium diisopropyl amide 作用下， 以 四氢呋喃 为溶剂， 以77%的产率得到2,5-diiodo-3,4-dicyanothiophene
  参考文献：
  名称：

  The Interplay of Bent-Shape, Lateral Dipole and Chirality in Thiophene Based Di-, Tri-, and Tetracatenar Liquid Crystals

  摘要：

  A range of mesogenic molecules varying in both bend angle and strength of lateral dipole were synthesized, and their phase behavior was characterized by polarizing microscopy, thermal analysis, X-ray diffraction, and electrooptical measurements. We find the general destabilization of the liquid crystallinity caused by strong lateral dipolar groups and the bent molecular shape are off-set in mesomorphic tetracatenars, which display stable nematic, smectic, columnar, and cubic mesophases. The broad mesomorphism of the tetracatenars containing lateral dipoles and their incompatibility with chiral induction are explained by considering that loosely correlated dimers exist within the mesophases. Chiral mesophases of derivatives with strong lateral dipoles were achieved by attaching fewer or different side chains to each end of the mesogen.

  DOI：

  10.1021/ja0268027

文献信息

• [EN] OLIGOTHIOPHENES DERIVATIVES<br/>[FR] DÉRIVÉS OLIGOTHIOPHÈNES
  申请人：UNIV BRUXELLES

  公开号：WO2011020712A3

  公开（公告）日：2011-05-12