4,14,24,34-tetraphenyl-[3,5,13,15,23,25,33,35]octaoxa[41,42,43,44]tetraaza[4,14,24,34]-tetraborapentacyclo[31.3.1.1(7,11).1(27,31)]dotriaconta-1(41),7,9,11(42),17,19,21(43),27,29,31(44),37,39-dodecaene | 201684-06-2

• 英文名称: 4,14,24,34-tetraphenyl-[3,5,13,15,23,25,33,35]octaoxa[41,42,43,44]tetraaza[4,14,24,34]-tetraborapentacyclo[31.3.1.1(7,11).1(27,31)]dotriaconta-1(41),7,9,11(42),17,19,21(43),27,29,31(44),37,39-dodecaene
• CAS: 201684-06-2
• 化学式: C₅₂H₄₈B₄N₄O₈
• 分子量: 900.219
• InChiKey: IBBVOSYHOSJBCC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  None
• 重原子数：
  None
• 可旋转键数：
  None
• 环数：
  None
• sp3杂化的碳原子比例：
  None
• 拓扑面积：
  None
• 氢给体数：
  None
• 氢受体数：
  None

反应信息

• 作为产物：
  描述：

  2,6-吡啶二甲醇 、 苯硼酸 以 乙酸乙酯 为溶剂， 以93%的产率得到4,14,24,34-tetraphenyl-[3,5,13,15,23,25,33,35]octaoxa[41,42,43,44]tetraaza[4,14,24,34]-tetraborapentacyclo[31.3.1.1(7,11).1(27,31)]dotriaconta-1(41),7,9,11(42),17,19,21(43),27,29,31(44),37,39-dodecaene
  参考文献：
  名称：

  New macrocyclic oligoboronates

  摘要：

  Two new macrocyclic oligoboronates were prepared in easy one step syntheses from aminodialcohols and phenylboronic acid. Reaction of 2,6-pyridinedimethanol gives a tetrameric species, while 2-(salicylideneamino)-1-hydroxyethane provides a cyclobisboronate. Both compounds are characterized by using X-ray structural analyses. Possible applications in the supramolecular host-guest chemistry an discussed. (C) 1997 Elsevier Science S.A.

  DOI：

  10.1016/s0022-328x(97)00183-6