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1-(4-ferrocenyl-1,2,3-triazol-1-yl)-1'-azidoferrocene | 1359734-38-5

中文名称
——
中文别名
——
英文名称
1-(4-ferrocenyl-1,2,3-triazol-1-yl)-1'-azidoferrocene
英文别名
——
1-(4-ferrocenyl-1,2,3-triazol-1-yl)-1'-azidoferrocene化学式
CAS
1359734-38-5
化学式
C22H18Fe2N6
mdl
——
分子量
478.119
InChiKey
GBGNHBDJUWHMQR-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    描述:
    1-(4-ferrocenyl-1,2,3-triazol-1-yl)-1'-azidoferrocene2-氟萘烯甲醛三甲基膦四氢呋喃 为溶剂, 以60%的产率得到1-(4-ferrocenyl-1,2,3-triazol-1-yl)-1'-[N-(fluoren-2-yl)methylene]aminoferrocene
    参考文献:
    名称:
    Synthesis, Structural Characterization, and Sensing Properties of Clickable Unsymmetrical 1,1′-Disubstituted Ferrocene–Triazole Derivatives
    摘要:
    A variety of unsymmetrically 1,1'-disubstituted ferrocenes 3-5 have been prepared by using the tandem click reaction/Staudinger-azaWittig process and their cation complexation properties studied using electrochemical and spectroscopic techniques. The common structural features present in these ligands are the presence of another redox unit, connected to the 1-position of the central ferrocene core through a triazole ring, and a photoactive moiety linked to the 1'-position of such core through an imine group. Receptors 3 and 5 undergo perturbation of the CV in the presence of Pb2+ and Zn2+ cations, whereas receptor 4 undergoes a different type of perturbation in the presence of Ni2+, Cd2+, Zn2+, and Pb2+ cations. The low-energy band of the absorption spectra of receptor 3 is blue-shifted, upon addition of Zn2+, and Pb2+ cations, whereas receptor 4 in the presence of Ni2+ and Cd2+ undergoes a remarkable red shift (Delta lambda = 110 nm) of the LE band which is responsible for the change of color from red to blue. Moreover, receptor 3 underwent a significant increase in its emission band in the presence of Pb2+, whereas in receptor 5, such an increase is notably lower. In conclusion, receptor 4 behaves as a colorimetric: receptor for Ni2+ and Cd2+ and 5 acts as a selective fluorescent receptor for the Pb2+ cation. On the basis of the H-1 NMR titration data and from the DFT theoretical calculations, tentative binding modes have been proposed for the metal complexes formed.
    DOI:
    10.1021/om300093c
  • 作为产物:
    描述:
    二茂铁乙炔 、 1,1′-diazidoferrocene 在 CuSO4*5H2O 、 sodium ascorbate 作用下, 以 四氢呋喃 为溶剂, 以41%的产率得到1-(4-ferrocenyl-1,2,3-triazol-1-yl)-1'-azidoferrocene
    参考文献:
    名称:
    Synthesis, Structural Characterization, and Sensing Properties of Clickable Unsymmetrical 1,1′-Disubstituted Ferrocene–Triazole Derivatives
    摘要:
    A variety of unsymmetrically 1,1'-disubstituted ferrocenes 3-5 have been prepared by using the tandem click reaction/Staudinger-azaWittig process and their cation complexation properties studied using electrochemical and spectroscopic techniques. The common structural features present in these ligands are the presence of another redox unit, connected to the 1-position of the central ferrocene core through a triazole ring, and a photoactive moiety linked to the 1'-position of such core through an imine group. Receptors 3 and 5 undergo perturbation of the CV in the presence of Pb2+ and Zn2+ cations, whereas receptor 4 undergoes a different type of perturbation in the presence of Ni2+, Cd2+, Zn2+, and Pb2+ cations. The low-energy band of the absorption spectra of receptor 3 is blue-shifted, upon addition of Zn2+, and Pb2+ cations, whereas receptor 4 in the presence of Ni2+ and Cd2+ undergoes a remarkable red shift (Delta lambda = 110 nm) of the LE band which is responsible for the change of color from red to blue. Moreover, receptor 3 underwent a significant increase in its emission band in the presence of Pb2+, whereas in receptor 5, such an increase is notably lower. In conclusion, receptor 4 behaves as a colorimetric: receptor for Ni2+ and Cd2+ and 5 acts as a selective fluorescent receptor for the Pb2+ cation. On the basis of the H-1 NMR titration data and from the DFT theoretical calculations, tentative binding modes have been proposed for the metal complexes formed.
    DOI:
    10.1021/om300093c
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