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2,8,14,20-Tetraoxatricyclo[19.3.1.19,13]hexacosa-1(25),9(26),10,12,21,23-hexaene-11,23-dicarbonyl chloride | 142763-09-5

中文名称
——
中文别名
——
英文名称
2,8,14,20-Tetraoxatricyclo[19.3.1.19,13]hexacosa-1(25),9(26),10,12,21,23-hexaene-11,23-dicarbonyl chloride
英文别名
——
2,8,14,20-Tetraoxatricyclo[19.3.1.19,13]hexacosa-1(25),9(26),10,12,21,23-hexaene-11,23-dicarbonyl chloride化学式
CAS
142763-09-5
化学式
C24H26Cl2O6
mdl
——
分子量
481.373
InChiKey
FNPZKSIOKJFBCC-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    6.4
  • 重原子数:
    32
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    71.1
  • 氢给体数:
    0
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Recognition of axial ligands by a zinc porphyrin host on the basis of nonpolar interligand interaction
    摘要:
    A porphyrin host with a preorganized cavity on each face has been synthesized and characterized. The constants for association of the zinc complex of the porphyrin with various amine ligands were determined and compared with those of [meso-tetrakis(p-methylphenyl)porphyrinato]zinc(II) and of a "picket-fence" porphyrin zinc(II) complex. The selectivity for the amine ligands was not observed for the picket-fence porphyrin complex. Contrary to this, small secondary amines, such as azetidine, pyrrolidine, and diethylamine, that fit the shape of the cavity of the synthesized host complex bind more strongly to the host than less hindered amines, such as butylamine and propylamine; the recognition parameters for azetidine versus butylamine were found to be K = 22, DELTA-H-degrees = -2.6 kcal/mol, and T-DELTA-S-degrees = -0.8 kcal/mol at 25-degrees-C in toluene. However, the binding of the larger secondary amines such as dipropylamine and diisopropylamine to the host was weakened due to greater steric repulsions from the cavity. It was concluded that, in this case, the stabilization of the ligand binding by the geometrical complementarity between the amines and the cavity of the host is ascribed mainly to attractive interligand interactions such as the London force or CH-pi interaction.
    DOI:
    10.1021/ja00043a016
  • 作为产物:
    描述:
    3,3',5,5'-bis(1,5-pentanediyldioxy)dibenzoic acid氯化亚砜 作用下, 反应 3.0h, 以95%的产率得到2,8,14,20-Tetraoxatricyclo[19.3.1.19,13]hexacosa-1(25),9(26),10,12,21,23-hexaene-11,23-dicarbonyl chloride
    参考文献:
    名称:
    Recognition of axial ligands by a zinc porphyrin host on the basis of nonpolar interligand interaction
    摘要:
    A porphyrin host with a preorganized cavity on each face has been synthesized and characterized. The constants for association of the zinc complex of the porphyrin with various amine ligands were determined and compared with those of [meso-tetrakis(p-methylphenyl)porphyrinato]zinc(II) and of a "picket-fence" porphyrin zinc(II) complex. The selectivity for the amine ligands was not observed for the picket-fence porphyrin complex. Contrary to this, small secondary amines, such as azetidine, pyrrolidine, and diethylamine, that fit the shape of the cavity of the synthesized host complex bind more strongly to the host than less hindered amines, such as butylamine and propylamine; the recognition parameters for azetidine versus butylamine were found to be K = 22, DELTA-H-degrees = -2.6 kcal/mol, and T-DELTA-S-degrees = -0.8 kcal/mol at 25-degrees-C in toluene. However, the binding of the larger secondary amines such as dipropylamine and diisopropylamine to the host was weakened due to greater steric repulsions from the cavity. It was concluded that, in this case, the stabilization of the ligand binding by the geometrical complementarity between the amines and the cavity of the host is ascribed mainly to attractive interligand interactions such as the London force or CH-pi interaction.
    DOI:
    10.1021/ja00043a016
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文献信息

  • Synthesis and Axial-Ligand Binding of Zinc Complexes of Amphiphilic Porphyrins Containing a Hydrophobic Binding Pocket
    作者:Hiroyasu Imai、Hiroki Munakata、Atsuko Takahashi、Shigeo Nakagawa、Yoshio Uemori
    DOI:10.1246/cl.1997.819
    日期:1997.8
    Amphiphilic zinc porphyrins containing two sulfonate groups and a hydrophobic binding pocket were synthesized efficiently and characterized. Binding of pyridine, butylamine, and pyrrolidine to the zinc complexes was examined spectrophotometrically in water and in chloroform. The binding behavior was discussed on the basis of the binding constants.
    高效合成了含有两个磺酸基团和一个疏结合袋的两性卟啉盐,并对其进行了表征。在氯仿中用分光光度法检测了吡啶丁胺吡咯烷与络合物的结合情况。根据结合常数对结合行为进行了讨论。
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