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[(4-(2,2-dimethylhydrazino)dimethylhydrazone-3-penten-2-one)Cu(MeCN)] | 1355949-92-6

中文名称
——
中文别名
——
英文名称
[(4-(2,2-dimethylhydrazino)dimethylhydrazone-3-penten-2-one)Cu(MeCN)]
英文别名
——
[(4-(2,2-dimethylhydrazino)dimethylhydrazone-3-penten-2-one)Cu(MeCN)]化学式
CAS
1355949-92-6
化学式
C11H22CuN5
mdl
——
分子量
287.875
InChiKey
JNKNQSOGNHCQRE-SZNDJZPWSA-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

反应信息

  • 作为反应物:
    描述:
    [(4-(2,2-dimethylhydrazino)dimethylhydrazone-3-penten-2-one)Cu(MeCN)] 以 neat (no solvent, solid phase) 为溶剂, 生成 [(4-(2,2-dimethylhydrazino)dimethylhydrazone-3-penten-2-one)Cu]
    参考文献:
    名称:
    Cu(I)/O2 Chemistry Using a β-Diketiminate Supporting Ligand Derived from N,N-Dimethylhydrazine: A [Cu3O2]3+ Complex with Novel Reactivity
    摘要:
    A Cu(I) complex, LCu(CH3CN), was prepared and characterized, where L- is a sterically unencumbered beta-diketiminate ligand, the deprotonated version of 4-(2,2-dimethylhydrazino)dimethylhydrazone-3-penten-2-one (LH). Analysis of FTIR spectra of the products of the reaction of LCu(CH3CN) with CO indicate that L- is strongly electron donating, and support an equilibrium in solution between monomeric and dimeric forms with terminal and bridging CO ligands, respectively. Low temperature oxygenation of LCu(CH3CN) generated a bis(mu-oxo)tricopper complex with a S = 1 [Cu3O2](3+) core that was identified on the basis of UV-vis (lambda(max) (epsilon, M-1 cm(-1) per Cu) = 328 (10700), 420 (1500), 590 (835) nm) and X-band electron paramagnetic resonance (EPR) spectroscopy (Delta m(s) = 2 transition at 1500 G), electrospray ionization (ESI) mass spectrometry, and spectrophotometric titration (0.35(2) equiv of O-2 per copper atom), magnetic susceptibility (mu(eff) = 2.8(1) BM), and H2O2 detection experiments (no H2O2 evolved upon acidification). Unlike other reported variants supported by neutral N-donor ligands, L3Cu3O2 is not reduced by ferrocene, does not abstract H-atoms from phenols or 1,2-dihydroanthracene, oxidizes PPh3 to Ph3P=O, and generates carbonate species upon exposure to CO2. This unique reactivity for a [Cu3O2](3+) complex may be traced to the anionic charge and strong electron donating characteristics of L-.
    DOI:
    10.1021/ic202214c
  • 作为产物:
    描述:
    乙腈荚基化铜 、 4-(2,2-dimethylhydrazino)dimethylhydrazone-3(Z)-penten-2-one 以 四氢呋喃乙腈 为溶剂, 以66%的产率得到[(4-(2,2-dimethylhydrazino)dimethylhydrazone-3-penten-2-one)Cu(MeCN)]
    参考文献:
    名称:
    Cu(I)/O2 Chemistry Using a β-Diketiminate Supporting Ligand Derived from N,N-Dimethylhydrazine: A [Cu3O2]3+ Complex with Novel Reactivity
    摘要:
    A Cu(I) complex, LCu(CH3CN), was prepared and characterized, where L- is a sterically unencumbered beta-diketiminate ligand, the deprotonated version of 4-(2,2-dimethylhydrazino)dimethylhydrazone-3-penten-2-one (LH). Analysis of FTIR spectra of the products of the reaction of LCu(CH3CN) with CO indicate that L- is strongly electron donating, and support an equilibrium in solution between monomeric and dimeric forms with terminal and bridging CO ligands, respectively. Low temperature oxygenation of LCu(CH3CN) generated a bis(mu-oxo)tricopper complex with a S = 1 [Cu3O2](3+) core that was identified on the basis of UV-vis (lambda(max) (epsilon, M-1 cm(-1) per Cu) = 328 (10700), 420 (1500), 590 (835) nm) and X-band electron paramagnetic resonance (EPR) spectroscopy (Delta m(s) = 2 transition at 1500 G), electrospray ionization (ESI) mass spectrometry, and spectrophotometric titration (0.35(2) equiv of O-2 per copper atom), magnetic susceptibility (mu(eff) = 2.8(1) BM), and H2O2 detection experiments (no H2O2 evolved upon acidification). Unlike other reported variants supported by neutral N-donor ligands, L3Cu3O2 is not reduced by ferrocene, does not abstract H-atoms from phenols or 1,2-dihydroanthracene, oxidizes PPh3 to Ph3P=O, and generates carbonate species upon exposure to CO2. This unique reactivity for a [Cu3O2](3+) complex may be traced to the anionic charge and strong electron donating characteristics of L-.
    DOI:
    10.1021/ic202214c
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