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[Cp(CO)2FeCH2(CH2)2CH=CH2] | 34788-97-1

中文名称
——
中文别名
——
英文名称
[Cp(CO)2FeCH2(CH2)2CH=CH2]
英文别名
——
[Cp(CO)2FeCH2(CH2)2CH=CH2]化学式
CAS
34788-97-1
化学式
C12H14FeO2
mdl
——
分子量
246.089
InChiKey
LCSCJHAXMCPCGL-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:
    [Cp(CO)2FeCH2(CH2)2CH=CH2]sodium hydroxide硼烷四氢呋喃络合物双氧水 作用下, 以 四氢呋喃 为溶剂, 以64%的产率得到
    参考文献:
    名称:
    The synthesis and characterisation of a new series of ω-hydroxy-alkyl complexes of iron
    摘要:
    omega-Hydroxy-alkyl compounds of the type, [Fe(eta(5)-C5R5){(CH2)(n)CH2OH}(CO)(2)] (R=H and Me, n =2-5, 7) were prepared by the oxidative hydroboration of the appropriate eta(1)-alkenyl compounds of the general formula, [Fe(eta(5)-C5R5){(CH2)(n-1)CH=CH2}(CO)(2)]. All new compounds were characterised by infrared, H-1 and C-13 NMR spectroscopy as well as mass spectrometry. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0277-5387(99)00252-1
  • 作为产物:
    描述:
    在 sodium iodide 作用下, 以 丙酮 为溶剂, 以69%的产率得到[Cp(CO)2FeCH2(CH2)2CH=CH2]
    参考文献:
    名称:
    Carbon-carbon bond formation by condensation of CpFe(CO)2(.eta.1-allyl) complexes with CpFe(CO)2(.eta.2-olefin) cations. Regio- and stereospecificity, sequential reactions leading to cycloadducts
    摘要:
    DOI:
    10.1021/ja00543a022
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文献信息

  • Synthesis and characterization of transition metal stabilized carbocations of the types [Cp∗(CO)2Fe{μ-(CnH2n−1}M(CO)xCp]PF6 (x=2, M=Fe or Ru; x=3, M=W, Cp∗=η5-C5(CH3)5; Cp=η5-C5H5; n=3–6) and [Cp(CO)2Ru{μ-(CnH2n−1)}W(CO)3Cp]PF6 (n=3–5) and the crystal structures of the complexes [Cp∗(CO)2Fe(CH2)3Ru(CO)2Cp], [Cp∗(CO)2Fe(CH2)5Ru(CO)2Cp], [Cp∗(CO)2Fe-(CH2)5W(CO)3Cp], and [Cp(CO)2Ru(CH2)5W(CO)3Cp]
    作者:Evans O. Changamu、Holger B. Friedrich、Melanie Rademeyer
    DOI:10.1016/j.jorganchem.2007.02.016
    日期:2007.5
    reported elsewhere. The structures of the precursor complexes [Cp∗(CO)2Fe(CH2)3Ru-(CO)2Cp] (1), [Cp∗(CO)2Fe(CH2)5Ru-(CO)2Cp] (2), [Cp∗(CO)2Fe(CH2)5W(CO)3Cp] (3), and [Cp(CO)2Ru (CH2)5W(CO)3Cp] (4), have been confirmed by single crystal X-ray crystallography. The structure of [Cp∗(CO)2Fe(CH2)3Ru(CO)2Cp] is compared with that of its corresponding cationic complex, [Cp∗(CO)2Feμ-(C3H5)}Ru(CO)2Cp]PF6.
    混合配体配合物的[CP * (CO)2的Fe(CH 2)ñ M(CO)X的CP](X  = 2,M = Fe或; X  = 3,M = W中,CP *  =η 5 - ç 5(CH 3)5 ; CP =η 5 -C 5 H ^ 5 ; ñ  = 3-6),键入我,与一当量氢化物提取器的Ph反应3 CPF 6,得到的过渡属稳定化的碳阳离子配合物[ CP ∗(CO)2 Fe μ-(C nH 2 n -1)} M(CO)x CP] PF 6。同样,新的II型异质双属配合物[CP(CO)2 Ru μ-(C n H 2 n -1)} W(CO)3 CP]与Ph 3 CPF 6反应生成碳正离子配合物[CP( CO)2 Ru μ-(C n H 2 n -1)} W(CO)3 CP] PF 6。光谱数据表明,氢化物从亚甲基β选择性地发生到与CP *配体连接的属原子上我很复杂。在式II的复合物
  • Reactivity studies on some η1-alkenyl complexes of iron
    作者:Leone Hermans、Selwyn F. Mapolie
    DOI:10.1016/s0277-5387(96)00295-1
    日期:1997.1
    The eta(1)-alkenyl complexes [eta(5)-C5H5(CO)(2)Fe(CH2)(n)CH=CH2] (n = 2 and 3) have been prepared by the reaction of Na[eta(5)-C5H5(CO)(2)Fe] with 4-bromo-1-butene and 5-bromo-1-pentene respectively. The reactivity of the sigma-olefin complexes in hydrogenation, hydroboration and hydroformylation reactions are reported as are reactions with Lewis acids such as TiCl4 and the electrophile HCl. Copyright (C) 1996 Elsevier Science Ltd
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