2,3-bis(2,4,6-trimethylphenyl)bicyclo[2.2.2]oct-2-ene | 243980-43-0

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 二苯乙烯类
• 英文名称: 2,3-bis(2,4,6-trimethylphenyl)bicyclo[2.2.2]oct-2-ene
• CAS: 243980-43-0
• 化学式: C₂₆H₃₂
• 分子量: 344.54
• InChiKey: MGXXHYSTNRJFDF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.4
• 重原子数：
  26
• 可旋转键数：
  2
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.46
• 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：

  2,3-bis(2,4,6-trimethylphenyl)bicyclo[2.2.2]oct-2-ene 在 EA⁽¹⁺⁾*SbCl₆^(1-) 作用下， 以 二氯甲烷 为溶剂， 以100%的产率得到2,3-Bis-(2,4,6-trimethyl-phenyl)-bicyclo[2.2.2]oct-2-ene; compound with GENERIC INORGANIC NEUTRAL COMPONENT
  参考文献：
  名称：

  Vicinal-diaryl interactions in stilbenoid hydrocarbons as observed in the through-space charge delocalization of their cation radicals

  摘要：

  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。

  DOI：

  10.1139/v99-081
• 作为产物：
  描述：

  在 nitric oxide 作用下， 以 二氯甲烷 为溶剂， 生成 2,3-bis(2,4,6-trimethylphenyl)bicyclo[2.2.2]oct-2-ene
  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

• Silver(I) Complexation of (Poly)aromatic Ligands. Structural Criteria for Depth Penetration into <i>cis</i>-Stilbenoid Cavities
  作者：S. V. Lindeman、R. Rathore、J. K. Kochi

  DOI：10.1021/ic000770b

  日期：2000.12.1

  Silver(I) complexes with aromatic donors an thoroughly analyzed (with aid of the Cambridge Crystallographic Database) to identify the basic structural factors inherent to the bonding of an arene ligand. Most strikingly, the distance parameter d (which simply measures the normal separation of Ag from the mean aromatic plane) is singularly invariant at d = 2.41 +/- 0.05 Angstrom for all silver/arene complexes, independent of the hapticity (eta (1) or eta (2)), hybridization, or multiple coordination. As such, a systematic series of stilbenoid ligands has been successfully designed to precisely modulate the penetration of silver(I) into the ligand cleft, and a multicentered poly(arene) ligand (X) designed to form a one-dimensional assembly of Ag/arene units. Simply stated, the depth penetration of silver(I) into the aromatic cavities of various cis-stilbenoid donors can be precisely predicted with a single parameter gamma that measures the separation of the two cofacial aryl groups comprising the cleft. This simple geometric consideration must be taken into account in any successful-design of novel (poly)aromatic ligands for silver(I) complexation to constitute new molecular architectures.