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Os3(μ-H)2(μ3-1-OC10H6)(CO)9 | 61917-01-9

中文名称
——
中文别名
——
英文名称
Os3(μ-H)2(μ3-1-OC10H6)(CO)9
英文别名
——
Os3(μ-H)2(μ3-1-OC10H6)(CO)9化学式
CAS
61917-01-9
化学式
C19H8O10Os3
mdl
——
分子量
966.867
InChiKey
SUZOFIKEFSNFGD-UHFFFAOYSA-M
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:
    Os3(μ-H)2(μ3-1-OC10H6)(CO)9 在 HBF4 作用下, 以 乙醚甲苯 为溶剂, 以25%的产率得到Os3(μ-H)2(μ3-1-OC10H6)(CO)9
    参考文献:
    名称:
    Reactions of the triosmium cluster Os3(μ-H)(μ-OH)(CO)10 with naphthols
    摘要:
    Reaction of the cluster Os-3(mu-H)(mu-OH)(CO)(10) (1) with 1-naphthol afforded the isomeric clusters 2a and 3a with the formulae OS3(mu-H)(2)(mu(3)-1-OC10H6)(CO)(9). A similar reaction with 2-naphthol, however, gave Os-3(mu-H)(mu-2-OC10H7)C)(10), 4b, and the analogue of 2a. These clusters have been structurally characterised to confirm the mode of anchoring of the naphthols. (C) 2003 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2003.08.030
  • 作为产物:
    描述:
    decacarbonyl-1κ(4)C,2κ(3)C,3κ(3)C-μ-hydrido-2:3κ(2)H-μ-hydroxy-2:3κ(2)O-trisosmium-(3 Os-Os) 、 萘酚 在 HBF4 作用下, 以 甲苯 为溶剂, 以85%的产率得到Os3(μ-H)2(μ3-1-OC10H6)(CO)9
    参考文献:
    名称:
    Reactions of the triosmium cluster Os3(μ-H)(μ-OH)(CO)10 with naphthols
    摘要:
    Reaction of the cluster Os-3(mu-H)(mu-OH)(CO)(10) (1) with 1-naphthol afforded the isomeric clusters 2a and 3a with the formulae OS3(mu-H)(2)(mu(3)-1-OC10H6)(CO)(9). A similar reaction with 2-naphthol, however, gave Os-3(mu-H)(mu-2-OC10H7)C)(10), 4b, and the analogue of 2a. These clusters have been structurally characterised to confirm the mode of anchoring of the naphthols. (C) 2003 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2003.08.030
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文献信息

  • Metallation of hydroxy-aryl and -alkyl compounds by reaction with dodecacarbonyl-triangulo-triosmium
    作者:Kazi A. Azam、Antony J. Deeming、Richard E. Kimber、Padmaja R. Shukla
    DOI:10.1039/dt9760001853
    日期:——
    ROH react with [OS3(CO)12] at 140 °C to give species of type [Os(CO)10H(OR)](R = Ph, 2-naphthyl, CHMe2. CH2Ph, CHMePh, or CMe2Ph), some of which convert at higher temperatures into the dihydrides [Os3(CO)9H2(X)], the second metal hydride being derived from R. Where hydrogen-atom transfer is from the β-carbon atom, compounds containing the triply bridged ligand X (X = OC6H4, 2-OC10H6, 1-OC10H6, or OC6H3OH-o)
    各种有机羟基化合物ROH与[OS反应3(CO)12 ]在140℃,得到类型的物种[OS(CO)10 H(OR)(R =苯基,2-基,CHME 2。CH 2 Ph,CHMEPh或CMe 2 Ph),其中一些在较高温度下转化为二氢化物[OS 3(CO)9 H 2(X)],第二种氢化物衍生自R。其中氢原子转移来自的β碳原子,含有该化合物三重桥接配位体X(X = OC 6 H ^ 4,2-OC 10 ħ 6,1-OC 10 H ^ 6,或OC 6形成H 3 OH- o),而γ-碳氢键裂解使带有X的物质桥接两个原子,并与其中一个形成五元螯合环(X = OCMe 2 C 6 H 4,OCHMEC 6 H 4或1-OC 10 H 6)。讨论了这些结论的光谱证据。
  • Organo-Group 15 derivatives of triosmium clusters containing naphthyl ligands
    作者:Mien Wei Lum、Weng Kee Leong
    DOI:10.1016/j.ica.2003.09.001
    日期:2004.2
    Reactions of the clusters Os-3(mu-H)(2)(mu(3)-1-OC10H6)(CO)(9), 1, and Os-3(mu-H)(mu-2-OC10H7)(CO)(10), 2, with the group 15 ligands EPh3 (E = P, As, Sb) generally afforded the mono- and, or disubstituted derivatives. These derivatives tend to decompose during chromatographic separations on silica gel; thus one of the decomposition products from the reaction of 1 with PPh3 has been identified as Os(H)(2)(CO)(2)(PPh3)(2), 3. The molecular structures of 3, as well as the derivatives Os-3(mu-H)(2)(mu(3)-1-OC10H6)(CO)(8)(AsPh3), 4, Os-3(mu-H)(2)(mu(3)-1-OC10H6)(CO)(7)(SbPh3)(2), 5c, Os-3(mu-H)(mu-2-OC10H7)(CO)(8)(AsPh3)(2), 7b, and Os-3(mu-H)(mu-2-OC10H7)(CO)(8)(SbPh3)(2), 7c, have been determined by single crystal X-ray diffraction studies. (C) 2003 Elsevier B.V. All rights reserved.
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