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[Ru(η3-C(CCC6H4-4-Me)=C(H)C6H4-4-Me)(PMe3)4]BF4 | 1092095-98-1

中文名称
——
中文别名
——
英文名称
[Ru(η3-C(CCC6H4-4-Me)=C(H)C6H4-4-Me)(PMe3)4]BF4
英文别名
——
[Ru(η3-C(CCC6H4-4-Me)=C(H)C6H4-4-Me)(PMe3)4]BF4化学式
CAS
1092095-98-1
化学式
BF4*C30H51P4Ru
mdl
——
分子量
723.505
InChiKey
IRYSJUUIXWJVSG-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:
    [Ru(η3-C(CCC6H4-4-Me)=C(H)C6H4-4-Me)(PMe3)4]BF4 在 Me2Mg 作用下, 以 四氢呋喃 为溶剂, 以49%的产率得到[Ru(C(CCC6H4-4-Me)=C(H)C6H3-4-Me)(PMe3)4]
    参考文献:
    名称:
    Formation of Ruthenaindenes by Cyclometalation of Ruthenium(II) Diarylbutenyne Complexes
    摘要:
    The reaction of diarylbutenynylruthenium complexes [Ru(eta(3)-C CC(6)H(4)R)=C(R')C(6)H(4)R)-(PMe(3))(4)](+) (C(6)H(4)R = C(6)H(4)R = C(6)H(4)-4-'Bu, Ph, C(6)H(4)-4-Me; R' = H, Me) with dimethylinagnesium yields the cyclometalated ruthenaidene complexes [Ru(C(C CC(6)H(4)R)=C(R')'C(6)H(3)R)(PMe(3))(4)] with ruthenium incorporated into the five-membered ring of an indene. The reaction involves the initial formation of methylruthenium complexes, which then rearrange with the elimination of methane to yield the product, The complexes [Ru(C(C CC(6)H(4)R)=C(R')C(6)H(3)R)(PMe(3))(4)] (C(6)H(4)R = C(6)H(4)-4-'Bu, R' = H; C(6)H(4)R = Ph, R' = Me) were crystallographically characterized.
    DOI:
    10.1021/om900613y
  • 作为产物:
    描述:
    2,6-lutidinium tetrafluoroboratetrans-Ru[CC-(p-C6H4Me)]2(PMe3)4四氢呋喃 为溶剂, 以48%的产率得到[Ru(η3-C(CCC6H4-4-Me)=C(H)C6H4-4-Me)(PMe3)4]BF4
    参考文献:
    名称:
    Butenynyl and Vinylidene Complexes of Ruthenium
    摘要:
    Reaction of ruthenium bis-acetylide complexes with 2,6-lutidinium tetrafluoroborate gave butenynyl complexes cis-[Ru(eta(3)-RC CC=C(H)R)(PMe(3))(4)]BF(4) in moderate to good yields. The structure of cis[Ru(eta(3)-tBuC CC=C(H)tBu)(PMe(3))(4)]BF(4) was determined crystallographically. Attempts to prepare cis[Ru(eta(3)-MeC CC=C(H)Me)(PMe(3))(4)]BF(4) resulted in the formation of two isomers, which differ in the stereochemistry about the double bond. The reaction of two bis-acetylide complexes with methyl triflate afforded butenynyl-type complexes cis- [Ru(eta(3)-RC CC=C(Me)R)(PMe(3))(4)](+) (R = Me, Ph). The mixed acetylide-vinylidene complex trans-[Ru(C CSiMe(3))(C=CH(2))(PMe(3))(4)]PF(6) was prepared by the reaction of trans-Ru(C CSiMe(3))(2)(PMe(3))(4) with ammonium hexafluorophosphate. In addition, the crystal structure of trans-[Ru(C CH)(C=CH(2))(PMe(3))(4)]BF(4) is reported.
    DOI:
    10.1021/om800861g
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