2,12,19,29-tetraoxo-1,4,7,10,13,18,21,24,27,30-decaaza-4,7,10,21,24,27-cyclotetratriacontanehexaacetic acid | 221903-71-5

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 大环内酰胺类
• 英文名称: 2,12,19,29-tetraoxo-1,4,7,10,13,18,21,24,27,30-decaaza-4,7,10,21,24,27-cyclotetratriacontanehexaacetic acid
• 英文别名: 2-[4,10,21,24,27-Pentakis(carboxymethyl)-2,12,19,29-tetraoxo-1,4,7,10,13,18,21,24,27,30-decazacyclotetratriacont-7-yl]acetic acid
• CAS: 221903-71-5
• 化学式: C₃₆H₆₂N₁₀O₁₆
• 分子量: 890.946
• InChiKey: YQVCNYHVBOZMMA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -17.1
• 重原子数：
  62
• 可旋转键数：
  12
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.72
• 拓扑面积：
  360
• 氢给体数：
  10
• 氢受体数：
  22

反应信息

• 作为反应物：
  描述：

  gadolinium(III) carbonate 、 2,12,19,29-tetraoxo-1,4,7,10,13,18,21,24,27,30-decaaza-4,7,10,21,24,27-cyclotetratriacontanehexaacetic acid 以 水 为溶剂， 生成
  参考文献：
  名称：

  Binuclear Gd³⁺ Complex of a 34-Membered Macrocycle with Six Carboxymethyl Arms:  X-ray Structures, Formation Constants, NMR, EPR, and ¹H NMR Relaxivities

  摘要：

  A 34-membered macrocyclic ligand with six pendant carboxymethyl groups has been synthesized by the coupling of two diethylenetriaminepentaacetate (dtpa) and two 1,4-diaminoburane units: the macrocycle is 2,12,19,29-tetraoxo-1,4,7,10,13,18,21,24,27,30-decaaza-4,7,10,21,24,27-cyclotetratriacontanehexaacetic acid, abbreviated as (34dtpabn)H-6. The macrocycle was crystallized as the acetone adduct (34dtpabn)H-6. 2Me(2)CO in the monoclinic space group P2(1)/n with a = 14.566(2) Angstrom, b = 10.968(1) Angstrom, c = 16.133(2) Angstrom, beta = 105.62(1)degrees, and Z = 2. The acetone molecules have close contacts with some carbon atoms of the macrocycle. The protonation constants determined by potentiometric titration (0.1 M KCl, 25 degrees C) were log K-1 = 9.70 (standard deviation = 0.01), log K-2 = 9.18 (0.05), log K-3 = 5.27 (0.02), log K-4 = 4.50 (0.03), log K-5 = 3.84 (0.01), and log K-6 = 3.23 (0.01). The corresponding protonation sites were identified by the pD dependence of H-1 NMR shifts; the central amino nitrogen of each dtpa moiety has the highest basicity. The binuclear Gd3+ complex of the macrocycle was crystallized as the 2-propanol adduct [Gd-2(34dtpabn)(H2O)(2)]. 2PrOH . 7H(2)O in the triclinic space group P (1) over bar with a = 11.880(1) Angstrom, b = 15.036(1) Angstrom, c = 17.396(1) Angstrom, alpha = 94.986(5)degrees, beta = 103.340(5)degrees, gamma = 98.286(5)degrees, and Z = 2. Each ligand molecule coordinates two Gd3+ ions forming a binuclear metal chelate with the Gd-Gd distance 10.8928(7) Angstrom. The coordination geometry around each metal ion is a tricapped trigonal prism consisting of three carboxylate oxygens, two amide oxygens, three amino nitrogens, and a water oxygen. Propanol molecules are located near the macrocyclic cavity with some close C-C contacts shorter than the sum of the van der Waals radii of methyl and methylene groups. The logarithmic overall formation constants, log beta(GdpLHr), were determined by potentiometry (0.1 M KCl, 25 degrees C): for GdLH4, 35.85 (estimated uncertainty = 0.21); GdLH3, 33.89 (0.36); GdLH2, 30.27 (0.07); GdLH, 25.59 (0.04); GdL, 16.46 (0.04); GdLH-1, 4.93 (0.19); Gd2L, 30.36 (0.33). Dipolar interaction operative between the two Gd3+ ions in the binuclear complex collapses the hyperfine structure in the EPR spectrum. The H-1 NMR relaxivities are enhanced as a result of the binuclear complex formation.

  DOI：

  10.1021/ic981015p