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[CuCl(2,6-[1-(2,6-diisopropylphenylimino)ethyl]pyridine)(C10N7)]*methylisobutylketone | 852528-84-8

中文名称
——
中文别名
——
英文名称
[CuCl(2,6-[1-(2,6-diisopropylphenylimino)ethyl]pyridine)(C10N7)]*methylisobutylketone
英文别名
——
CAS
852528-84-8
化学式
C6H12O*C10N7*C33H43ClCuN3
mdl
——
分子量
899.041
InChiKey
ASAKTPIWMVUKQS-VRCYMSAESA-M
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:
    [CuBr(2,6-[1-(2,6-diisopropylphenylimino)ethyl]pyridine)]PF6tetraethylammonium 1,1,2,4,5,5-hexacyano-3-azapentadienide4-甲基-2-戊酮丙酮 为溶剂, 以75%的产率得到[CuCl(2,6-[1-(2,6-diisopropylphenylimino)ethyl]pyridine)(C10N7)]*methylisobutylketone
    参考文献:
    名称:
    Organocyanide coordination chemistry: Syntheses, structural characterisations and magnetic properties of copper (II) complexes with a di-imine/pyridine ligand
    摘要:
    The reactions between the copper (11) salts [CuXL]PF6 (L: 2,6-[1-(2,6-d iisopropylphenylimino)ethyl]pyridine) (X = Cl 1, X = Br 2) and LiTCNQ, in a DMF/water mixture, or Et3NH(TCNQ)(2), in acetone, produced the new complexes [CuXL(TCNQ)] (X = Cl 3, X = Br 4). For both compounds, crystallographic studies have clearly evidenced the existence of dimeric complexes [{CuClL}(TCNQ)](2) owing to pi-pi overlap between two adjacent TCNQ(center dot-) radical anions. Compound 1 reacted with Et4N(C10N7) to afford the mononuclear derivative [CuC1L(C10N7)] (5), while its reaction with K2C10N6 produced the dinuclear complex [(CuClL)(2)(C10N6)] (6). The crystal structures of complexes 5 and 6 have been determined by X-ray crystallography. Magnetic studies have revealed that compound 6 displays weak antiferromagnetic interactions between the two metal centres, conversely compounds 3 and 5 exhibit purely paramagnetic behaviours. (c) 2005 Elsevier B.V.. All rights reserved.
    DOI:
    10.1016/j.ica.2005.02.011
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