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7,9:16,18-dinaphthyl-1,3,4,6,10,12,13,15-octaazacyclooctadecane-1,5,10,14-tetraene | 1263407-20-0

中文名称
——
中文别名
——
英文名称
7,9:16,18-dinaphthyl-1,3,4,6,10,12,13,15-octaazacyclooctadecane-1,5,10,14-tetraene
英文别名
3,6,18,21-Tetramethyl-2,4,5,7,17,19,20,22-octazapentacyclo[21.7.1.18,12.027,31.016,32]dotriaconta-1(30),2,6,8,10,12(32),13,15,17,21,23,25,27(31),28-tetradecaene
7,9:16,18-dinaphthyl-1,3,4,6,10,12,13,15-octaazacyclooctadecane-1,5,10,14-tetraene化学式
CAS
1263407-20-0
化学式
C28H28N8
mdl
——
分子量
476.584
InChiKey
QTWZVLFWQKUCIH-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):
    3.3
  • 重原子数:
    36
  • 可旋转键数:
    0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    115
  • 氢给体数:
    4
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    7,9:16,18-dinaphthyl-1,3,4,6,10,12,13,15-octaazacyclooctadecane-1,5,10,14-tetraene 、 cobalt(II) chloride 以 甲醇 为溶剂, 以72%的产率得到Cl2Co(7,9:16,18-dinaphthyl-1,3,4,6,10,12,13,15-octaazacyclooctadecane-1,5,10,14-tetraene)
    参考文献:
    名称:
    Synthesis, Physicochemical, and Antimicrobial Screening Studies of Complexes of Co(II), Ni(II), Cu(II), and Zn(II) with 18-membered Schiff Base Octaazamacrocyclic Ligand
    摘要:
    A [2 + 2] condensation reaction between 1,8-diaminonaph-thalene and N,N'-diacetylhydrazine in 1:1 molar ratio in methanol resulted in a novel Schiff base macrocyclic ligand, (L): 7,9:16,18-dinaphthyl-1,3,4,6,10,12,13,15-octaazacyclooctadecane-1,5,10,14-tetraene. Metal complexes have been synthesized by the reaction of L with the corresponding metal salts. The results of elemental analyses, ESI-mass, and Job's method ascertain their stoichiometry while the spectral data obtained from 1H and 13C NMR, and IR confirmed their bonding features. However, the stereochemistry was inferred from the UV-visible, EPR, and magnetic moment studies. The ligand and its complexes were screened in vitro against gram positive bacteria, gram negative bacteria, and fungi.
    DOI:
    10.1080/15533174.2010.522650
  • 作为产物:
    参考文献:
    名称:
    Synthesis, Physicochemical, and Antimicrobial Screening Studies of Complexes of Co(II), Ni(II), Cu(II), and Zn(II) with 18-membered Schiff Base Octaazamacrocyclic Ligand
    摘要:
    A [2 + 2] condensation reaction between 1,8-diaminonaph-thalene and N,N'-diacetylhydrazine in 1:1 molar ratio in methanol resulted in a novel Schiff base macrocyclic ligand, (L): 7,9:16,18-dinaphthyl-1,3,4,6,10,12,13,15-octaazacyclooctadecane-1,5,10,14-tetraene. Metal complexes have been synthesized by the reaction of L with the corresponding metal salts. The results of elemental analyses, ESI-mass, and Job's method ascertain their stoichiometry while the spectral data obtained from 1H and 13C NMR, and IR confirmed their bonding features. However, the stereochemistry was inferred from the UV-visible, EPR, and magnetic moment studies. The ligand and its complexes were screened in vitro against gram positive bacteria, gram negative bacteria, and fungi.
    DOI:
    10.1080/15533174.2010.522650
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文献信息

  • Synthesis, Physicochemical, and Antimicrobial Screening Studies of Complexes of Co(II), Ni(II), Cu(II), and Zn(II) with 18-membered Schiff Base Octaazamacrocyclic Ligand
    作者:Tahir Ali Khan、Sultana Naseem、Rafat Hajra、Mohammad Shakir
    DOI:10.1080/15533174.2010.522650
    日期:2010.11.30
    A [2 + 2] condensation reaction between 1,8-diaminonaph-thalene and N,N'-diacetylhydrazine in 1:1 molar ratio in methanol resulted in a novel Schiff base macrocyclic ligand, (L): 7,9:16,18-dinaphthyl-1,3,4,6,10,12,13,15-octaazacyclooctadecane-1,5,10,14-tetraene. Metal complexes have been synthesized by the reaction of L with the corresponding metal salts. The results of elemental analyses, ESI-mass, and Job's method ascertain their stoichiometry while the spectral data obtained from 1H and 13C NMR, and IR confirmed their bonding features. However, the stereochemistry was inferred from the UV-visible, EPR, and magnetic moment studies. The ligand and its complexes were screened in vitro against gram positive bacteria, gram negative bacteria, and fungi.
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