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(η(2)-C.tplbond.CPh)Co2(CO)6(CH2=CHSiCl2) | 182363-10-6

中文名称
——
中文别名
——
英文名称
(η(2)-C.tplbond.CPh)Co2(CO)6(CH2=CHSiCl2)
英文别名
——
(η(2)-C.tplbond.CPh)Co2(CO)6(CH2=CHSiCl2)化学式
CAS
182363-10-6
化学式
C16H8Cl2Co2O6Si
mdl
——
分子量
513.214
InChiKey
GHGLLOQHDSKZHA-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

  • 作为产物:
    描述:
    dicobalt octacarbonyl 、 dichloro(phenylethynyl)(vinyl)silane甲苯正戊烷 为溶剂, 以82%的产率得到(η(2)-C.tplbond.CPh)Co2(CO)6(CH2=CHSiCl2)
    参考文献:
    名称:
    Koordinationsverhalten vinyl- und alkinylfunktionalisierter chlorsilane
    摘要:
    The coordination ability of vinyl and alkynyl substituted chlorosilanes of type (H2C=CH)(R)SiCl2 (1a R = Cl, Ib R = CH3, 1c R = C=CPh), (H2C=CH)(PhC=C)(R)SiCl [1d R = N(SiMe(3))(2), 1e R = C=CPh], as well as of the disiloxane [(H2C=CH)(PhC=C)(2)Si]O-2 (11) towards different organometallic compounds, such as Fe-2(CO)(9) (2), MnCp(CO)(3) (4, Cp = eta(5)-C5H5) and Co-2(CO)(8) (6) is discussed. Treatment of the vinylchlorosilanes 1a and 1b with Fe-2(CO)(9) (2) or MnCp(CO)(3) (4) in n-pentane or n-hexane produces the compounds [(eta(2)-H2C=CH)ML(n)](R)SiCl2 [3a ML(n) = Fe(CO)(4), R = Cl; 3b ML(n) = Fe(CO)(4), R = CH3; 5a ML(n) = MnCp(CO)(2), R = Cl; 5b ML(n) = MnCp(CO)(2), R = CH3] in which the vinyl unit is eta(2)-coordinated to an Fe(CO)(4) or MnCp(CO)(2) moiety. While compounds la or Ib do not react with Co-2(CO)(8) (6) under similar applied reaction conditions, it is found that the alkynyl substituted chlorosilanes 1c-1e yield on addition of Co-2(CO)(8) the complexes [(eta(2)-C=CPh)Co-2(Co)(6)](H2C=CH)(R)SiCl [7a R = Cl, 7b R = N(SiMe(3))(2), 7e R = C=CPh] or [(eta(2)-C=CPh)Co-2(CO)(6)](2)(H2C=CH)SiCl (7d) respectively. In these compounds, the phenylethinyl ligands are eta(2)-coordinated to a Co-2(CO)(6) fragment, thus forming bulky dicobalta-tetrahedrane units. Hydrolysis of compound 7c produces the disiloxane {[(eta(2)-C=CPh)Co-2(CO)(6)](H2C=CH)(PhC=C)Si}O-2 (9). Additionally, this compound can be synthesized by the reaction of [(H2C=CH)(PhC=C)(2)Si]O-2 (11) with two equivalents of Co-2(CO)(8) (6). On treatment of 6 with one equivalent of the disiloxane 11 the formation of compound [(eta(2)-C=CPh)Co-2(CO)(6)](H2C=CH)(PhC=C)Si-O-Si(HC=CH2)(C=CPh)(2) (12) is obtained.All compounds were characterized by analytical and spectroscopic data (IR, H-1, C-13, Si-29 NMR, MS). The solid state structures of compounds [(eta(2)-C=CPh)Co-2(CO)(6)](H2C=CH)SiCl2 (7a) and [(eta(2)-C=CPh)Co-2(CO)(6)](H2C=CH)(PhC=C)SiCl (7c) are reported. Complexes 7a and 7c crystallize in the triclinic space group with the following cell parameters: 7a a = 816.8(3), b = 1597.5(9), c = 1601.5(8) pm, alpha = 101.49(4), beta = 100.01(4), gamma = 96.55(4)degrees, V = 2003(1) x 10(6) pm(3) and Z = 4; 7c a = 827.6(2), b = 914.0(2), c = 1696.7(5) pm, alpha = 89.35(2), beta = 76.75(2), gamma = 84.05(2)degrees, V = 1242(1) x 10(6) pm(3) and Z = 2.
    DOI:
    10.1016/0022-328x(96)06287-0
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