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(1',1'''-diisopropyl-1,1''-biferrocene)[Ni(mnt)2] | 474713-33-2

中文名称
——
中文别名
——
英文名称
(1',1'''-diisopropyl-1,1''-biferrocene)[Ni(mnt)2]
英文别名
——
(1',1'''-diisopropyl-1,1''-biferrocene)[Ni(mnt)2]化学式
CAS
474713-33-2
化学式
C8N4NiS4*C26H30Fe2
mdl
——
分子量
793.287
InChiKey
QVFIBUPQBAAOAR-NTPUEXKPSA-J
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:
    1′,1‴-diisopropyl-1,1″-biferrocene 、 ferrocenium bis(maleonitriledithiolato)nickel(III) 以 二氯甲烷丙酮 为溶剂, 以59%的产率得到(1',1'''-diisopropyl-1,1''-biferrocene)[Ni(mnt)2]
    参考文献:
    名称:
    Biferrocene−M(mnt)2 Charge-Transfer Complexes (M = Ni, Co; mnt = Maleonitriledithiolate). Structure, Valence States, and Magnetic Properties
    摘要:
    Charge-transfer salts of branched-alkyl biferrocenes, (1', 1"'-R-2-1,1"-biferrocene)[Ni(mnt)(2)] (1a, R = isopropyl; 2a, R = dineopentyl) and (1', 1"'-R2-1,1"-biferrocene)(2)[Co(mnt)(2)](2) (1b, R = isopropyl; 2b, R = dineopentyl), were prepared. Their valence states were investigated using X-ray crystallography and Mossbauer spectroscopy. Complexes 1a and 1b show segregated-stack crystal structures that contain columns of acceptors, whereas structures of 2a and 2b, which contain bulky donors, are rather discrete. All of the complexes contain mixed-valent biferrocenium monocations. A two-step valence transition was found in complex 1a. The crystal contains two crystal log raphically independent cations: one undergoes valence localization below room temperature; the other undergoes valence localization below ca. 130 K. The former transition is derived from asymmetry of the crystal environment around the cation, whereas the latter one is caused by symmetry lowering coupled with a spin-Peierls transition (T-C = 133.2 K) associated with the dimerization of the acceptors. This compound was found to exhibit a dielectric response based on valence tautomerization. Other complexes (1b, 2a, and 2b) show a valence-trapped state. In all complexes, charge localization was found to occur through local electrostatic interactions between the donor's cationic moiety and the acceptor's electronegative moieties.
    DOI:
    10.1021/ic048285u
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