1,3-Di-tert-butyl-benzo[b]naphtho[2,3-e][1,4]dioxine-6,11-dione | 131079-92-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 1,3-Di-tert-butyl-benzo[b]naphtho[2,3-e][1,4]dioxine-6,11-dione
• 英文别名: 2,4-Ditert-butylbenzo[b]oxanthrene-6,11-dione
• CAS: 131079-92-0
• 化学式: C₂₄H₂₄O₄
• 分子量: 376.452
• InChiKey: ADGLRWOALNIQPB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.3
• 重原子数：
  28
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  52.6
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  二(三甲基硅基)碳酰二亚胺 、 1,3-Di-tert-butyl-benzo[b]naphtho[2,3-e][1,4]dioxine-6,11-dione 在 四氯化钛 作用下， 以 二氯甲烷 为溶剂， 以96%的产率得到(2,4-Ditert-butyl-6-cyanoiminobenzo[b]oxanthren-11-ylidene)cyanamide
  参考文献：
  名称：

  Synthesis and electrochemical properties of benzo[b]naphtho[2,3-e][1,4]-dioxin-6,11-quinones and their N,N'-dicyano quinone diimine derivatives

  摘要：

  The reaction of 2,3-dichloro-1,4-naphthoquinone (1) and catechols 2 in pyridine affords a series of substituted benzo[b]naphtho[2,3-e][1,4]dioxin-6,11-quinones 3. The latter compounds are transformed to the corresponding N,N'-dicyano quinone diimines 4, by treating them with N,N'-bis(trimethylsilyl)carbodiimide. The electrochemical studies of compounds of the type 3 and 4 in DMF and CH2Cl2, respectively, by means of cyclic voltammetry are reported. The experimental reduction potentials provide information on electron-electron repulsion in the dianionic states of 3 and 4, and hence on their potential use as acceptor components in charge-transfer complexes and organic conductors.

  DOI：

  10.1021/jo00004a042
• 作为产物：
  描述：

  2,3-二氯-1,4-萘醌 、 3,5-二叔丁基邻苯二酚 在 吡啶 作用下， 反应 6.0h， 以58%的产率得到1,3-Di-tert-butyl-benzo[b]naphtho[2,3-e][1,4]dioxine-6,11-dione
  参考文献：
  名称：

  Synthesis and electrochemical properties of benzo[b]naphtho[2,3-e][1,4]-dioxin-6,11-quinones and their N,N'-dicyano quinone diimine derivatives

  摘要：

  The reaction of 2,3-dichloro-1,4-naphthoquinone (1) and catechols 2 in pyridine affords a series of substituted benzo[b]naphtho[2,3-e][1,4]dioxin-6,11-quinones 3. The latter compounds are transformed to the corresponding N,N'-dicyano quinone diimines 4, by treating them with N,N'-bis(trimethylsilyl)carbodiimide. The electrochemical studies of compounds of the type 3 and 4 in DMF and CH2Cl2, respectively, by means of cyclic voltammetry are reported. The experimental reduction potentials provide information on electron-electron repulsion in the dianionic states of 3 and 4, and hence on their potential use as acceptor components in charge-transfer complexes and organic conductors.

  DOI：

  10.1021/jo00004a042

文献信息

• シアノ基含有化合物及び電子写真感光体
  申请人：京セラドキュメントソリューションズ株式会社

  公开号：JP2021006512A

  公开（公告）日：2021-01-21

  【課題】感光層に含有された場合に、電子写真感光体の感度特性を向上させる化合物の提供。【解決手段】式（１−Ｙ１）又は式（１−Ｙ２）で表される化合物。［Ｘ１及びＸ２は、各々独立に、Ｏ又はＳ；Ｒ１及びＲ２は、各々独立に、Ｃ１−８アルキル基等；ｍは、０〜４の整数；ｎは、０〜６の整数］【選択図】図１

  【问题】提供一种可以提高电子照相感光体感光层中感光性能的化合物。 【解决方法】化合物由式（1-Y1）或式（1-Y2）表示。[其中，X1和X2分别独立为O或S；R1和R2分别独立为C1-8烷基等；m为0-4的整数；n为0-6的整数]。 【选定图】图1。
• CZEKANSKI, TOMASZ;HANACK, MICHAEL;BECKER, JAMES Y.;BERNSTEIN, JOEL;BITTNE+, J. ORG. CHEM., 56,(1991) N, C. 1569-1573
  作者：CZEKANSKI, TOMASZ、HANACK, MICHAEL、BECKER, JAMES Y.、BERNSTEIN, JOEL、BITTNE+

  DOI：——

  日期：——
• JP2022018811A
  申请人：——

  公开号：——

  公开（公告）日：——
• Synthesis and electrochemical properties of benzo[b]naphtho[2,3-e][1,4]-dioxin-6,11-quinones and their N,N'-dicyano quinone diimine derivatives
  作者：Tomasz Czekanski、Michael Hanack、James Y. Becker、Joel Bernstein、Shmuel Bittner、Leah Kaufman-Orenstein、Dina Peleg

  DOI：10.1021/jo00004a042

  日期：1991.2

  The reaction of 2,3-dichloro-1,4-naphthoquinone (1) and catechols 2 in pyridine affords a series of substituted benzo[b]naphtho[2,3-e][1,4]dioxin-6,11-quinones 3. The latter compounds are transformed to the corresponding N,N'-dicyano quinone diimines 4, by treating them with N,N'-bis(trimethylsilyl)carbodiimide. The electrochemical studies of compounds of the type 3 and 4 in DMF and CH2Cl2, respectively, by means of cyclic voltammetry are reported. The experimental reduction potentials provide information on electron-electron repulsion in the dianionic states of 3 and 4, and hence on their potential use as acceptor components in charge-transfer complexes and organic conductors.