3,6,13,24,31,34-Hexaoxa-40-azahexacyclo[34.3.1.07,12.014,23.016,21.025,30]tetraconta-1(40),7,9,11,14,16,18,20,22,25,27,29,36,38-tetradecaene | 131354-61-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 3,6,13,24,31,34-Hexaoxa-40-azahexacyclo[34.3.1.07,12.014,23.016,21.025,30]tetraconta-1(40),7,9,11,14,16,18,20,22,25,27,29,36,38-tetradecaene
• CAS: 131354-61-5
• 化学式: C₃₃H₂₉NO₆
• 分子量: 535.596
• InChiKey: HMXAYWSXEUSPAR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.9
• 重原子数：
  40
• 可旋转键数：
  0
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  68.3
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  四氢呋喃 、 3,6,13,24,31,34-Hexaoxa-40-azahexacyclo[34.3.1.07,12.014,23.016,21.025,30]tetraconta-1(40),7,9,11,14,16,18,20,22,25,27,29,36,38-tetradecaene 反应 12.0h， 生成
  参考文献：
  名称：

  Macroring-neutral molecule complexation. Synthesis of biconcave pyridino hosts, complex formation, and x-ray crystal structures of two inclusion compounds

  摘要：

  A series of pyridino macrocycles 1-3(a-e) incorporating rigid bi- and triaryl ether segments in different ring positions have been synthesized. The effect of incorporation of these building blocks into a given macroring framework on the host properties for uncharged-molecule inclusion has been studied. Symmetric 21-membered macrorings 1c, 1d, or 2c, 2d with tri-o-phenylene, tri-2,3-naphthylene, or mixed phenylene naphthylene ether units are efficient hosts in solid-state complexation of dipolar-aprotic and apolar guests such as nitro compounds and nitriles as well as DMF, DMSO, THF, dioxane, or benzene. X-ray analyses of the solid-state complexes of 1d with PhNO2 (1:1) and MeCN (1:1) have been studied. It is shown that the presence of the triaryl ether segment induces a biconcave nonequally sided host conformation suitable for guest inclusion. The packing characterizes the host-guest topologies of the two inclusion compounds to be of (H-bonded) cavitate-type for the MeCN case and of interstitial channel type for the PhNO2 case. A comparative discussion of the present and previous results support the interpretation of hemispherand preorganization for the new host structures.

  DOI：

  10.1021/jo00003a055
• 作为产物：
  描述：

  2-[3-(2-hydroxyphenoxy)naphthalen-2-yl]oxyphenol 在 palladium on activated charcoal 氢气 、 sodium hydride 、 caesium carbonate 作用下， 以 四氢呋喃 、 乙酸乙酯 为溶剂， 25.0~80.0 ℃ 、303.98 kPa 条件下， 反应 15.0h， 生成 3,6,13,24,31,34-Hexaoxa-40-azahexacyclo[34.3.1.07,12.014,23.016,21.025,30]tetraconta-1(40),7,9,11,14,16,18,20,22,25,27,29,36,38-tetradecaene
  参考文献：
  名称：

  Macroring-neutral molecule complexation. Synthesis of biconcave pyridino hosts, complex formation, and x-ray crystal structures of two inclusion compounds

  摘要：

  A series of pyridino macrocycles 1-3(a-e) incorporating rigid bi- and triaryl ether segments in different ring positions have been synthesized. The effect of incorporation of these building blocks into a given macroring framework on the host properties for uncharged-molecule inclusion has been studied. Symmetric 21-membered macrorings 1c, 1d, or 2c, 2d with tri-o-phenylene, tri-2,3-naphthylene, or mixed phenylene naphthylene ether units are efficient hosts in solid-state complexation of dipolar-aprotic and apolar guests such as nitro compounds and nitriles as well as DMF, DMSO, THF, dioxane, or benzene. X-ray analyses of the solid-state complexes of 1d with PhNO2 (1:1) and MeCN (1:1) have been studied. It is shown that the presence of the triaryl ether segment induces a biconcave nonequally sided host conformation suitable for guest inclusion. The packing characterizes the host-guest topologies of the two inclusion compounds to be of (H-bonded) cavitate-type for the MeCN case and of interstitial channel type for the PhNO2 case. A comparative discussion of the present and previous results support the interpretation of hemispherand preorganization for the new host structures.

  DOI：

  10.1021/jo00003a055

文献信息

• WEBER, EDWIN;KOHLER, HANS-JURGEN;REUTER, HANS, J. QRG. CHEM., 56,(1991) N, C. 1236-1242
  作者：WEBER, EDWIN、KOHLER, HANS-JURGEN、REUTER, HANS

  DOI：——

  日期：——