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| 156030-15-8

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
156030-15-8
化学式
C10H8O4W
mdl
——
分子量
376.021
InChiKey
NDWDMGKAOJCZHY-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:
    甲苯 为溶剂, 生成 ((13)CO)10(μ-H)[C(O)CH2(W((13)CO)3(cyclopentadienyl))triosmium]
    参考文献:
    名称:
    Synthesis of Unsaturated Os3W2 and Metastable Os4W Oxo-Ethylidyne Clusters by Solid-State Pyrolysis. Direct C-O Bond Cleavage of a Coordinated Ketenyl Ligand
    摘要:
    Heterometallic ketenyl complex OS3(CO)10(mu-H)[C(O)CH2(W(CO)3CP)] (1a) possessing a pendant CPW(CO)3 substituent was prepared by condensation Of OS3(CO)10(NCMe)2 with the metal-aldehyde compleX CPW(CO)3CH2CHO. Pyrolysis of 1a in the solid state at 185-degrees-C afforded two heteropentametallic cluster compounds, CP2W2OS3(CO)12(mu-O)(mu3-CMe) (2) and CPWOS4-(CO)12(mu-O)(mu3-CMe) (3), demonstrating a unique example of C-0 bond scission of a ligated ketene fragment and a cluster aggregation process. Complex 2 crystallizes in orthorhombic space group Pnma with a = 18.913(4) angstrom, b = 16.229(3) angstrom, c = 9.129(2) angstrom, Z = 4, R = 0.054, and R(w) = 0.055 for 2551 observed reflections. The W2Os3 cluster that contains 72 cluster valence electrons has a distorted square-pyramidal array of metal atoms with one Os-H-Os hydride ligand, one bridging oxo ligand associated with a W-W double bond, and an ethylidyne ligand bridging a unique W2Os triangle. Crystals of 3 are monoclinic of space group P2(1)/n with a = 15.941(2) angstrom, b = 19.395(4) angstrom, c = 16.369(4) angstrom, beta = 94.72(2)-degrees, Z = 8, R = 0.050, and R(w) = 0.041 for 6568 observed reflections. This molecule possesses a WOS4 trigonal-bipyramidal skeleton with an oxo ligand bridging a W-Os edge and an ethylidyne ligand capping a WOS2 face, Isomerization of 3 occurred upon dissolution at room temperature to afford edge-bridging tetrahedral cluster CpWOS4(CO)12(mu3-0)(mu3-CMe) (4), in which the oxo ligand formally migrated from an edge-bridging to a face-bridging position. Pyrolysis of 4 in the solid state at 190-degrees-C regenerated 3 in h gh yield, suggesting the existence of a delicate equilibrium between these two cluster complexes. Crystal data for 4: space group P2(1)/n, a = 9.492(3) angstrom, b = 16.990(2) angstrom, c = 15.887(3) angstrom, beta = 98.79(2)-degrees, Z = 4. The structure was solved by direct methods and refined to R and R(w) values of 0.039 and 0.032 for 4455 observed reflections with I > 2sigma(I).
    DOI:
    10.1021/om00017a032
  • 作为产物:
    描述:
    氯乙醛 、 (η(5)-cyclopentadienyl)tricarbonyltungstanate 生成
    参考文献:
    名称:
    Synthesis of Unsaturated Os3W2 and Metastable Os4W Oxo-Ethylidyne Clusters by Solid-State Pyrolysis. Direct C-O Bond Cleavage of a Coordinated Ketenyl Ligand
    摘要:
    Heterometallic ketenyl complex OS3(CO)10(mu-H)[C(O)CH2(W(CO)3CP)] (1a) possessing a pendant CPW(CO)3 substituent was prepared by condensation Of OS3(CO)10(NCMe)2 with the metal-aldehyde compleX CPW(CO)3CH2CHO. Pyrolysis of 1a in the solid state at 185-degrees-C afforded two heteropentametallic cluster compounds, CP2W2OS3(CO)12(mu-O)(mu3-CMe) (2) and CPWOS4-(CO)12(mu-O)(mu3-CMe) (3), demonstrating a unique example of C-0 bond scission of a ligated ketene fragment and a cluster aggregation process. Complex 2 crystallizes in orthorhombic space group Pnma with a = 18.913(4) angstrom, b = 16.229(3) angstrom, c = 9.129(2) angstrom, Z = 4, R = 0.054, and R(w) = 0.055 for 2551 observed reflections. The W2Os3 cluster that contains 72 cluster valence electrons has a distorted square-pyramidal array of metal atoms with one Os-H-Os hydride ligand, one bridging oxo ligand associated with a W-W double bond, and an ethylidyne ligand bridging a unique W2Os triangle. Crystals of 3 are monoclinic of space group P2(1)/n with a = 15.941(2) angstrom, b = 19.395(4) angstrom, c = 16.369(4) angstrom, beta = 94.72(2)-degrees, Z = 8, R = 0.050, and R(w) = 0.041 for 6568 observed reflections. This molecule possesses a WOS4 trigonal-bipyramidal skeleton with an oxo ligand bridging a W-Os edge and an ethylidyne ligand capping a WOS2 face, Isomerization of 3 occurred upon dissolution at room temperature to afford edge-bridging tetrahedral cluster CpWOS4(CO)12(mu3-0)(mu3-CMe) (4), in which the oxo ligand formally migrated from an edge-bridging to a face-bridging position. Pyrolysis of 4 in the solid state at 190-degrees-C regenerated 3 in h gh yield, suggesting the existence of a delicate equilibrium between these two cluster complexes. Crystal data for 4: space group P2(1)/n, a = 9.492(3) angstrom, b = 16.990(2) angstrom, c = 15.887(3) angstrom, beta = 98.79(2)-degrees, Z = 4. The structure was solved by direct methods and refined to R and R(w) values of 0.039 and 0.032 for 4455 observed reflections with I > 2sigma(I).
    DOI:
    10.1021/om00017a032
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