8,11,14,17,23,24-hexaazatricyclo[17.3.1.12,6]tetracosa-1(23),2,4,6(24),19,21-hexaene-8,11,14,17-tetraacetic acid | 1198592-47-0

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: 8,11,14,17,23,24-hexaazatricyclo[17.3.1.12,6]tetracosa-1(23),2,4,6(24),19,21-hexaene-8,11,14,17-tetraacetic acid
• 英文别名: 2-[8,14,17-Tris(carboxymethyl)-8,11,14,17,23,24-hexazatricyclo[17.3.1.12,6]tetracosa-1(22),2,4,6(24),19(23),20-hexaen-11-yl]acetic acid；2-[8,14,17-tris(carboxymethyl)-8,11,14,17,23,24-hexazatricyclo[17.3.1.12,6]tetracosa-1(22),2,4,6(24),19(23),20-hexaen-11-yl]acetic acid
• CAS: 1198592-47-0
• 化学式: C₂₆H₃₄N₆O₈
• 分子量: 558.591
• InChiKey: SMJSUYTYVPVSON-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -9.7
• 重原子数：
  40
• 可旋转键数：
  8
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  188
• 氢给体数：
  4
• 氢受体数：
  14

反应信息

• 作为产物：
  描述：

  8,11,14,17,23,24-hexaazatricyclo[17.3.1.12,6]tetracosa-1(23),2,4,6(24),19,21-hexaene-8,11,14,17-tetraacetic acid 8,11,14,17-tetrakis(1,1-dimethylethyl) ester 在 甲酸 作用下， 反应 24.0h， 以100%的产率得到8,11,14,17,23,24-hexaazatricyclo[17.3.1.12,6]tetracosa-1(23),2,4,6(24),19,21-hexaene-8,11,14,17-tetraacetic acid
  参考文献：
  名称：

  An efficient route to pyridine and 2,2′-bipyridine macrocycles incorporating a triethylenetetraminetetraacetic acid core as ligand for lanthanide ions

  摘要：

  Two novel macrocyclic chelators L-1 and L-2 incorporating an intracyclic pyridine or 2,2'-bipyridine unit and a triethylenetetraminetetraacetic acid core (TITA) were synthesized with the aim of forming lanthanide complexes suitable as efficient long-lived luminophores. For this goal, an efficient methodology for the preparation of TITA derivatives using prealkylated precursors is described Starting from commercially available compounds, the target ligands were obtained in seven (L-1) and nine (L-2) steps in 40% and 20% overall yields. respectively. Stable Tb(III) complexes were prepared and displayed interesting luminescence properties. (C) 2009 Elsevier Ltd All rights reserved

  DOI：

  10.1016/j.tetlet.2009.09.030

文献信息

• Polyazamacrocycles based on a tetraaminoacetate moiety and a (poly)pyridine intracyclic unit: direct synthesis and application to the photosensitization of Eu(III) and Tb(III) ions in aqueous solutions
  作者：Ghassan Bechara、Nadine Leygue、Chantal Galaup、Béatrice Mestre-Voegtlé、Claude Picard

  DOI：10.1016/j.tet.2010.09.052

  日期：2010.11

  A series of five new 15-, 18- or 21-membered polyazamacrocycles (L-1-L-5) based on a pyridine, bipyridine or terpyridine unit and a triethylenetetraminetetraacetic acid (TTTA) skeleton is described. In ligands L-4 and L-5 the azaheterocycle contains an additional extracyclic functionality (ester group) suitable for covalently attachment to bioactive molecules. The synthetic procedure is based on the use of a linear tetra-N-alkylated tetramine synthon incorporating masked acetate arms and an efficient metal template ion effect, which controls the crucial macrocyclization step. In the case of L-1-L-3, the formation of lanthanide complexes with europium(III) and terbium(III) was investigated and the fluorescence characteristics of the complexes were established. In this series, the terbium(III) complex derived from the bipyridine ligand exhibits the highest lifetime and quantum yield values (tau=2.18 ms, Phi=26%). (C) 2010 Elsevier Ltd. All rights reserved.