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| 1100051-53-3

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1100051-53-3
化学式
C35H54FeO2Si
mdl
——
分子量
590.745
InChiKey
GCCPBAIRTJXFDN-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:
    描述:
    参考文献:
    名称:
    Giant Dendritic Molecular Electrochrome Batteries with Ferrocenyl and Pentamethylferrocenyl Termini
    摘要:
    Giant redox dendrimers were synthesized with ferrocenyl and pentamethylferrocenyl termini up to a theoretical number of 39 tethers (seventh generation). Lengthening of the tethers proved to be a reliable strategy to overcome the bulk constraint at the dendrimers periphery. These redox metallodendrimers were characterized by H-1, C-13, and Si-29 NMR; MALDI-TOF mass spectrometry (for the low generations); elemental analysis; UV-vis spectroscopy; dynamic light scattering (DLS); atomic force microscopy (AFM); electron-force microscopy (EFM) for hall- or fully oxidized dendrimers; cyclic voltammetry; and coulometry. UV-vis spectroscopy, coulometry, and analytical data are consistent with an increasing amount of defects as the generation number increases, with this amount remaining relatively weak up to G(5). AFM shows that the dendrimers form aggregates of discrete size on the mica surface, recalling the agglomeration of metal atoms in monodisperse nanoparticles. Cyclic voltarnmetry reveals full chemical and electrochemical reversibility up to G(7), showing that electron transfer is fast among the flexible peripheral redox sites. Indeed, the redox stability of these new electrochromic dendrimers, i.e., a battery behavior, was established by complete chemical oxido-reduction cycles, and the blue 17-electron ferrocenium and deep-green mixed-valence Fe(III)/Fe(II) dendritic complexes were isolated and characterized. AFM studies also show the reversible dendrimer size changes from upon redox switching between Fe(II) and Fe(III), suggesting a breathing mechanism controlled by the redox potential. Considerable adsorption of high-generation dendrimers on Pt electrodes such as G(7)-Fc allows the easy formation of modified electrodes that sense the ATP anion only involving the electrostatic factor even in the absence of any other type of interaction with the redox tethers.
    DOI:
    10.1021/ja8062343
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