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| 163455-85-4

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
163455-85-4
化学式
C63H54GaN3O6
mdl
——
分子量
1018.86
InChiKey
WRWGRLBZSHWVCG-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

  • 作为产物:
    参考文献:
    名称:
    Metal-Induced Self-Assembly of a Pyrene-Tethered Hydroxamate Ligand for the Generation of Multichromophoric Supramolecular Systems. The Pyrene Excimer as Switch for Iron(III)-Driven Intramolecular Fluorescence Quenching
    摘要:
    We report the first example of intramolecular excimer formation in supramolecular trichromophoric systems resulting from the metal-directed self-assembly of chromophore-labeled ligand molecules. The trichromophoric gallium(III) chelate, (1)(3)Ga, shows an intense pyrene excimer fluorescence emission in acetonitrile, while the iron(III) analogue, (1)(3)Fe, exhibits a fluorescence of very low intensity compared to that of the free hydroxamate ligand 1. The trivalent gallium metal cation is demonstrated to play the role of an inert and transparent linker, whereas the ferric center acts additionally as an extra chromophore that quenches the pyrene singlet state. On the basis of low-temperature fluorescence measurements, the mechanism of quenching within (l)(3)Fe is attributed to a pyrene-to-iron electronic energy transfer process. (1)H NMR and electronic absorption spectroscopies show that intramolecular interactions between pyrene chromophores prevail in the ground state, which leads to the formation of preassociated excimers for both chelates. From the dependence of the solvent on the photophysical properties of (1)3Ga and (1)3Fe, it is inferred that the Fe(III)-induced quenching process is triggered by the ground-state and excited-state intramolecular dimerization of the pyrene moieties, with the pyrene-to-iron energy transfer taking place more readily from the excimer singlet state as donor than from the locally excited state.
    DOI:
    10.1021/ja980368k
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