octamethyl-9,10-dihydro-9,10-ethanoanthracene | 216664-83-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 蒽
• 英文名称: octamethyl-9,10-dihydro-9,10-ethanoanthracene
• 英文别名: 3,4,5,6,10,11,12,13-Octamethyltetracyclo[6.6.2.02,7.09,14]hexadeca-2,4,6,9,11,13-hexaene
• CAS: 216664-83-4
• 化学式: C₂₄H₃₀
• 分子量: 318.502
• InChiKey: DRXKNRWYMDWKNS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.2
• 重原子数：
  24
• 可旋转键数：
  0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为反应物：
  描述：

  octamethyl-9,10-dihydro-9,10-ethanoanthracene 在 nitric oxide 作用下， 以 二氯甲烷 为溶剂， 生成
  参考文献：
  名称：

  Novel Arene Receptors as Nitric Oxide (NO) Sensors

  摘要：

  Nitric oxide sensors are based on the reversible, specific, and efficient binding to various types of arene receptors via intermolecular complexes, which are characterized by complete electron delocalization and strong interaction between the donor and acceptor moieties.

  DOI：

  10.1021/ja020217o
• 作为产物：
  描述：

  在 nitric oxide 作用下， 以 二氯甲烷 为溶剂， 生成 octamethyl-9,10-dihydro-9,10-ethanoanthracene
  参考文献：
  名称：

  Novel Arene Receptors as Nitric Oxide (NO) Sensors

  摘要：

  Nitric oxide sensors are based on the reversible, specific, and efficient binding to various types of arene receptors via intermolecular complexes, which are characterized by complete electron delocalization and strong interaction between the donor and acceptor moieties.

  DOI：

  10.1021/ja020217o

文献信息

• Vicinal-diaryl interactions in stilbenoid hydrocarbons as observed in the through-space charge delocalization of their cation radicals
  作者：Rajendra Rathore、Jay K Kochi

  DOI：10.1139/v99-081

  日期：1999.6.1

  The conformational preference of vicinal or 1,2-phenyl groups is probed in two classes of ring-substituted 1,2-diphenylbicyclooctene (stilbenoid) hydrocarbons 1a-1d and 2a-2c. UV-vis spectroscopy reveals, and X-ray crystallography verifies, the intramolecular (edge-to-face) orientation for the phenyl-phenyl interaction in stilbenoids 1a-1d. Most importantly, when two pairs of ortho-methyl substituents are present, the cofacial phenyl groups in the stilbenoid donors are established by X-ray crystallography and spectrally observed in the cation radicals (2a^+.-2c^+.) by the appearance of new bands with strong absorptions in the near IR with λ_max = 1100-1315 nm, analogous to those previously observed in intermolecular (aromatic) interactions of aromatic cation radicals.Key words: stilbenoid hydrocarbon, cation radical, aryl-aryl interaction.

  在两类环替代的1,2-二苯基双环辛烷（stilbenoid）碳氢化合物1a-1d和2a-2c中，探测了邻位或1,2-苯基的构象偏好。UV-vis光谱揭示了，X射线晶体学证实了，stilbenoid 1a-1d中苯-苯相互作用的分子内（边缘对面）取向。最重要的是，当存在两对邻甲基取代基时，在X射线晶体学中建立了stilbenoid供体中的同面苯基团，并通过在阳离子自由基（2a+. -2c+.）中出现具有强吸收的新带，其λmax = 1100-1315 nm，类似于以前观察到的芳香族阳离子自由基的分子间（芳香族）相互作用。关键词：stilbenoid碳氢化合物，阳离子自由基，芳基-芳基相互作用。