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[(1,2-bis(diisopropylphosphino)ethane)Ni(C2H4)] | 111497-33-7

中文名称
——
中文别名
——
英文名称
[(1,2-bis(diisopropylphosphino)ethane)Ni(C2H4)]
英文别名
[(dippe)Ni(C2H4)]
[(1,2-bis(diisopropylphosphino)ethane)Ni(C2H4)]化学式
CAS
111497-33-7
化学式
C16H36NiP2
mdl
——
分子量
349.099
InChiKey
KTYKAUHVVFSVST-UHFFFAOYSA-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:
    参考文献:
    名称:
    Novel Ni(0)-COT Complexes, Displaying Semiaromatic Planar COT Ligands with Alternating C−C and CC Bonds
    摘要:
    Reaction of (R2PC2H4PR2)Ni(C2H4) With COT gives the mononuclear complexes (R2PC2H4PR2)Ni(eta(2)-C8H8) (R = Pr-i la, Bu-t Ib). The COT ligand in la,b is planar with alternating C-C and C=C bonds, corresponding to a formal semiaromatic [C8H8](-) ligand. Reactions of la with ((Pr2PC2H4PPr2)-Pr-i-Pr-i)Ni(eta(2),eta(2)-C6H10) and of Ib with stoichiometric amounts of {((Bu2PC2H4PBu2)-Bu-t-Bu-t)Ni}(2)(mu-C6H6) or lithium afford the dinuclear complexes {((Pr2PC2H4PPr2)-Pr-i-Pr-i)Ni}(2){mu-eta(4)(1,2,5,6):eta(4)(3,4,7,8)-C8H8} (2a) and {((Bu2PC2H4PBu2)-Bu-t-Bu-t)Ni}(2)(mu-eta(2):eta(2)-C8H8) (2b; two isomers). The COT ligand in 2a is tub-shaped and olefinic, whereas in 2b (as in la,b) it is planar and semiaromatic. The products are characterized by IR, solution and solid-state NMR spectroscopy, and by X-ray structure analysis.
    DOI:
    10.1021/ja964210g
  • 作为产物:
    描述:
    参考文献:
    名称:
    Poerschke, Klaus-Richard, Angewandte Chemie, 1987, vol. 99, p. 1321 - 1322
    摘要:
    DOI:
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文献信息

  • Cleavage of Carbon−Carbon Bonds in Alkyl Cyanides Using Nickel(0)
    作者:Juventino J. García、Alma Arévalo、Nicole M. Brunkan、William D. Jones
    DOI:10.1021/om049700t
    日期:2004.8.1
    The reaction of the complex [(dippe)NiH](2) (1) with a variety of alkyl cyanides afforded nickel(0) compounds of the type [(dippe)Ni(eta(2)-RCN)], where R, = Me, Et, Pr, Pr-i, Bu-t, cyclopropyl, cyclobutyl, adamantyl (2-9, respectively). When compounds 2-9 were warmed to yield oxidative addition products, the thermal reaction proceeded only in the case of 2 to produce [(dippe)Ni(Me)(CN)](10). Photochemical activation did produce oxidative addition products from compounds 2-8, which rapidly evolved to the beta-elimination products of the organic moiety in most cases and to the formation of [(dippe)Ni(CN)(2)] (11). Reaction of 1 with acetonitrile in the presence of BPh3 gives [(dippe)Ni(eta(2)-MeCNBPh3)](12), which does not undergo thermal C-CN cleavage upon heating. X-ray crystal structures are reported for 10-12.
  • Poerschke, Klaus-Richard, Angewandte Chemie, 1987, vol. 99, p. 1321 - 1322
    作者:Poerschke, Klaus-Richard
    DOI:——
    日期:——
  • Novel Ni(0)-COT Complexes, Displaying Semiaromatic Planar COT Ligands with Alternating C−C and CC Bonds
    作者:Ingrid Bach、Klaus-Richard Pörschke、Bernd Proft、Richard Goddard、Carsten Kopiske、Carl Krüger、Anna Rufińska、Klaus Seevogel
    DOI:10.1021/ja964210g
    日期:1997.4.1
    Reaction of (R2PC2H4PR2)Ni(C2H4) With COT gives the mononuclear complexes (R2PC2H4PR2)Ni(eta(2)-C8H8) (R = Pr-i la, Bu-t Ib). The COT ligand in la,b is planar with alternating C-C and C=C bonds, corresponding to a formal semiaromatic [C8H8](-) ligand. Reactions of la with ((Pr2PC2H4PPr2)-Pr-i-Pr-i)Ni(eta(2),eta(2)-C6H10) and of Ib with stoichiometric amounts of ((Bu2PC2H4PBu2)-Bu-t-Bu-t)Ni}(2)(mu-C6H6) or lithium afford the dinuclear complexes ((Pr2PC2H4PPr2)-Pr-i-Pr-i)Ni}(2)mu-eta(4)(1,2,5,6):eta(4)(3,4,7,8)-C8H8} (2a) and ((Bu2PC2H4PBu2)-Bu-t-Bu-t)Ni}(2)(mu-eta(2):eta(2)-C8H8) (2b; two isomers). The COT ligand in 2a is tub-shaped and olefinic, whereas in 2b (as in la,b) it is planar and semiaromatic. The products are characterized by IR, solution and solid-state NMR spectroscopy, and by X-ray structure analysis.
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