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[Cr(μ-NPh)(HC(C(Me)NC6H3-i-Pr2)2)]2 | 945907-82-4

中文名称
——
中文别名
——
英文名称
[Cr(μ-NPh)(HC(C(Me)NC6H3-i-Pr2)2)]2
英文别名
[(i-Pr2Ph)2nacnacCr]2(μ-NPh)2
[Cr(μ-NPh)(HC(C(Me)NC6H3-i-Pr2)2)]2化学式
CAS
945907-82-4
化学式
C70H92Cr2N6
mdl
——
分子量
1121.53
InChiKey
PXKLYDHTRKBNOP-IHVPEPGGSA-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:
    Binding and Activation of Small Molecules by Three-Coordinate Cr(I)
    摘要:
    [(i-Pr2Ph)(2)nacnacCr](2)(mu-eta(2):eta(2)-N-2) (2) has been prepared and structurally characterized; it contains a bridging side-on bonded dinitrogen ligand with a N-N distance of 1.249(5) A. Reactions of this reactive Cr(I) synthon with various small molecules resulted in a series of unusual molecules and transformations; thus CO yielded the binuclear isocarbonyl [(i-Pr2Ph)(2)nacnacCr](2)(CO)(mu-eta(1):eta(1)-CO)(2), ethylene gave [(i-Pr2Ph)(2)nacnacCr](2)(mu-eta(2):eta(2)-C2H4), O-2 oxidatively added to produce (i-Pr2Ph)(2)nacnacCr(O)(2), and azobenzene afforded the product of NN bond cleavage [(i-Pr2Ph)(2)nacnacCr](2)(mu-NPh)(2). 2 can be prepared in good yield and affords a facile entry to low-coordinate Cr(I) coordination chemistry.
    DOI:
    10.1021/ja0725549
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文献信息

  • Inverted-Sandwich Dichromium(I) Complexes Supported by Two β-Diketiminates:  A Multielectron Reductant and Syntheses of Chromium Dioxo and Imido
    作者:Yi-Chou Tsai、Po-Yang Wang、Shin-An Chen、Jin-Ming Chen
    DOI:10.1021/ja072003i
    日期:2007.7.1
    Treatment of [Cr(mu-Cl)(Nacnac)](2) (Nacnac = HC(C(Me)NC6H3-i-Pr-2)(2)) with 2.5 equiv of KC8 in toluene allows the isolation of an inverted-sandwich toluene-bridged complex, (mu-eta(6):eta(6)-C7H8)[Cr(Nacnac)](2) (1), in 88.2% yield as a dark-purple solid. The valency of each Cr is determined to be I by X-ray absorption spectroscopy. The twelve Cr-C distances are moderately long and 1 readily undergoes an arene exchange reaction with benzene. As a result, 1 behaves as a two-Cr(Nacnac) synthetic equivalents upon reaction with appropriate substrates. For example, treatment of 1 with 2 equiv of O-2, 4 equiv of MesN(3) (Mes = 2,4,6-C6H2Me3), and Ph2N2 engenders the formation of a monomeric Cr(O)(2)(Nacnac) (2), Cr(NMes)(2)(Nacnac) (3), and (mu-NPh)(Nacnac)](2) (4), respectively. Complex 1 is therefore an 8-electron reductant.
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