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| 167284-85-7

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
167284-85-7
化学式
BF4*C12H10MnO3
mdl
——
分子量
343.952
InChiKey
CQWCHNCDTZZJDM-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:
    乙烯双(三苯基磷)铂二氯甲烷 为溶剂, 以92%的产率得到(PPh3)2Pt(C6H5C(CH3)CH2Mn(CO)3)
    参考文献:
    名称:
    η2-Binding of Styrenes to Pt(PPh3)2. The Effect of Precoordination of Manganese Tricarbonyl Cation to the Aromatic Ring
    摘要:
    The ability of the olefinic C=C double bond in styrenes to bind to Pt(PPh3)(2) is greatly increased by eta(6)-precoordination of Mn(CO)(3)(+) to the arene ring.
    DOI:
    10.1021/om990818x
  • 作为产物:
    描述:
    (acenaphthene)Mn(CO)3BF4 、 2-苯基-1-丙烯二氯甲烷 为溶剂, 以75%的产率得到
    参考文献:
    名称:
    η2-Binding of Styrenes to Pt(PPh3)2. The Effect of Precoordination of Manganese Tricarbonyl Cation to the Aromatic Ring
    摘要:
    The ability of the olefinic C=C double bond in styrenes to bind to Pt(PPh3)(2) is greatly increased by eta(6)-precoordination of Mn(CO)(3)(+) to the arene ring.
    DOI:
    10.1021/om990818x
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文献信息

  • Synthesis of Dimanganese Complexes from the Reduction of Cationic Tricarbonylmanganese Styrene Derivatives
    作者:Seung Uk Son、Su Seong Lee、Young Keun Chung
    DOI:10.1021/ja970099i
    日期:1997.8.1
    Styrene derivatives of the manganese tricabonyl cation have been synthesized through the reaction of Mn(CO)(5)BF4 with excess styrene derivatives in refluxing CH2Cl2, and their chemical reduction has been studied. Treatment of [(styrene)Mn(CO)(3)](+) (1(H)) with 1.0 equiv of Cp2Co in CH2Cl2 or THF led to isolation of bimetallic 2(H). Treatment of [(1,1-diphenylethylene)Mn(CO)(3)](+) (1(Ph)) with 1.0 equiv of Cp2Co in CH2Cl2 yielded three different bimetallic compounds, 2(Ph), 3(Ph), and 4(Ph). The molecular structures of 2(H), 2(Ph), 3(Ph), and 4(Ph), determined by X-ray crystallography, were quite different from those of known bimetallics. Compounds 2(H) and 2(Ph) have the eta(5):eta(3) bonding pattern, where a Mn(CO)(4) moiety is coordinated to the styrene in an eta(3)-fashion. Compound 3(Ph) has the eta(5):eta(5) bonding pattern with two Mn(CO)(3) moieties pi-coordinated to a ligand derived from a coupling of 1,1-diphenylethylenes through the ipso carbon atom. Compound 4(Ph) has a metal-metal bond with no bridging carbonyls; one of the manganese atoms is coordinated by 1,1-diphenylethylene and two carbonyls and the other by the Mn(CO)(5). There are multiple reduction pathways available to (arene)Mn(CO)(3)(+) cations having a vinyl substituent on the arene ring.
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