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(η-1,5-Cyclooctadien)(η-1'-phenyl-2',4'-cyclopentadienyl)cobalt

中文名称
——
中文别名
——
英文名称
(η-1,5-Cyclooctadien)(η-1'-phenyl-2',4'-cyclopentadienyl)cobalt
英文别名
——
(η-1,5-Cyclooctadien)(η-1'-phenyl-2',4'-cyclopentadienyl)cobalt化学式
CAS
——
化学式
C19H21Co
mdl
——
分子量
308.369
InChiKey
CDZAYQWQXWQIES-GHDUESPLSA-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

  • 作为反应物:
    描述:
    (η-1,5-Cyclooctadien)(η-1'-phenyl-2',4'-cyclopentadienyl)cobalt1,6-cyclodecadiyne正辛烷 为溶剂, 以19-26的产率得到(η4:η4-{3(4)}cyclobutadienophane)bis{(η5-(phenyl)cyclopentadienyl)cobalt}
    参考文献:
    名称:
    Reaction of 1,6-cyclodecadiyne and 1,8-cyclotetradecadiyne with substituted CpCo(cod)
    摘要:
    The yields of CpCo-capped cyclobutadiene superphane from 1,6-cyclodecadiyne (1) and (R-C5H4)Co(cod) varies considerably with the substituents R. Electron-withdrawing substituents give yields between 35 and 45 % while electron-donating substituents give very small yields. In the case of 1,8-cyclotetradecadiyne (2) such a dependence on R is much less pronounced. The reaction between 1 and 2 and the indenyl complex (eta5-C9H7)Co(cod) is also reported.
    DOI:
    10.1021/om00029a051
  • 作为产物:
    描述:
    1,5-环辛二烯lithium 作用下, 以 四氢呋喃 为溶剂, 以45.6%的产率得到(η-1,5-Cyclooctadien)(η-1'-phenyl-2',4'-cyclopentadienyl)cobalt
    参考文献:
    名称:
    A correlation between 13C and 59Co NMR data and the catalytic activity of organocobalt complexes in the synthesis of pyridine derivatives
    摘要:
    DOI:
    10.1016/0022-328x(84)80468-4
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文献信息

  • The preparation of finely divided metal powders and transition metal complexes using “organically solvated” magnesium
    作者:Helmut Bönnemann、Borislav Bogdanović、Rainer Brinkmann、Bernd Spliethoff、Da-Wei He
    DOI:10.1016/0022-328x(93)83004-f
    日期:1993.6
    Mg★ is an excellent in situ reducing agent for transition metal salts, giving highly reactive metal powders of Groups 8–12. In the presence of electron donor ligands, this reduction provides a useful one-step route to organotransition metal complexes. The application of 35 kHz ultrasound during the reaction improves the dispersity of the metal powders and enhances the yields of the complexes.
    用少量蒽在THF中处理市售镁粉会生成高活性形式的镁(Mg★)。Mg★是一种出色的过渡金属盐原位还原剂,可产生8-12组的高反应性金属粉末。在电子给体配体的存在下,这种还原为有机过渡金属配合物提供了有用的一步法。反应过程中施加35 kHz超声波可改善金属粉末的分散性,并提高配合物的收率。
  • Steuerung der katalytischen Pyridinsynthese aus Alkien and Nitrilien durch (η<sup>6</sup>-Borinato)-Liganden am Cobalt
    作者:Helmut Bönnemann、Werner Brijoux、Rainer Brinkmann、Willi Meurers
    DOI:10.1002/hlca.19840670630
    日期:1984.9.26
    Control of the Catalytic Synthesis of Pyridine from Alkynes and Nitriles by the (η6-Borinato)-Nigands at Cobalt
    吡啶的从炔烃和腈的催化合成的控制由(η 6 -Borinato)-Nigands在钴
  • Reaction of 1,6-cyclodecadiyne and 1,8-cyclotetradecadiyne with substituted CpCo(cod)
    作者:Rolf Gleiter、Georg Pflaesterer
    DOI:10.1021/om00029a051
    日期:1993.5
    The yields of CpCo-capped cyclobutadiene superphane from 1,6-cyclodecadiyne (1) and (R-C5H4)Co(cod) varies considerably with the substituents R. Electron-withdrawing substituents give yields between 35 and 45 % while electron-donating substituents give very small yields. In the case of 1,8-cyclotetradecadiyne (2) such a dependence on R is much less pronounced. The reaction between 1 and 2 and the indenyl complex (eta5-C9H7)Co(cod) is also reported.
  • A correlation between 13C and 59Co NMR data and the catalytic activity of organocobalt complexes in the synthesis of pyridine derivatives
    作者:Helmut Bönnemann、Werner Brijoux、Rainer Brinkmann、Willi Meurers、Richard Mynott、Wolfgang Von Philipsborn、Thomas Egolf
    DOI:10.1016/0022-328x(84)80468-4
    日期:1984.9
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