5,12-dicyanonaphthacene | 244299-34-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 并四苯
• 英文名称: 5,12-dicyanonaphthacene
• 英文别名: Tetracene-5,12-dicarbonitrile；tetracene-5,12-dicarbonitrile
• CAS: 244299-34-1
• 化学式: C₂₀H₁₀N₂
• 分子量: 278.313
• InChiKey: RJFMNWMCQXEPRC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.8
• 重原子数：
  22
• 可旋转键数：
  0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  47.6
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  萘并萘-5,12-二甲醛 在 吡啶 、 盐酸羟胺 、 乙酸酐 作用下， 反应 6.5h， 生成 5,12-dicyanonaphthacene
  参考文献：
  名称：

  Synthesis, Properties, and Ambipolar Organic Field-Effect Transistor Performances of Symmetrically Cyanated Pentacene and Naphthacene as Air-Stable Acene Derivatives

  摘要：

  5,12-Dicyanonaphthacene and 6,13-dicyanopentacene have been synthesized for the first time. The LUMO and HOMO levels are deepened as predicted and fabricated organic field-effect transistors (OFETs) showed ambipolar responses with carrier mobilities of 10(-3) cm(2)/V.s.

  DOI：

  10.1021/ol200145r

文献信息

• Synthesis, Properties, and Ambipolar Organic Field-Effect Transistor Performances of Symmetrically Cyanated Pentacene and Naphthacene as Air-Stable Acene Derivatives
  作者：Shuhei Katsuta、Daichi Miyagi、Hiroko Yamada、Tetsuo Okujima、Shigeki Mori、Ken-ichi Nakayama、Hidemitsu Uno

  DOI：10.1021/ol200145r

  日期：2011.3.18

  5,12-Dicyanonaphthacene and 6,13-dicyanopentacene have been synthesized for the first time. The LUMO and HOMO levels are deepened as predicted and fabricated organic field-effect transistors (OFETs) showed ambipolar responses with carrier mobilities of 10(-3) cm(2)/V.s.