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cis-(cis-1,2-bis(diphenylphosphino)propenePP')(tetracarbonyl)Mo(0) | 128025-88-7

中文名称
——
中文别名
——
英文名称
cis-(cis-1,2-bis(diphenylphosphino)propenePP')(tetracarbonyl)Mo(0)
英文别名
——
cis-(cis-1,2-bis(diphenylphosphino)propenePP')(tetracarbonyl)Mo(0)化学式
CAS
128025-88-7
化学式
C31H24MoO4P2
mdl
——
分子量
618.417
InChiKey
BAMQEECLBREBRL-JIEAFDILSA-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:
    Mo(CO)5(PPh2H) 在 t-BuOK 、 catalyst: t-BuOK 作用下, 以 四氢呋喃二乙二醇二甲醚 为溶剂, 生成 cis-(cis-1,2-bis(diphenylphosphino)propenePP')(tetracarbonyl)Mo(0)
    参考文献:
    名称:
    Molybdenum carbonyl complexes of di- and triphosphines: Hydrophosphination reactions of (HCCCH2PPh2) Mo(CO)5
    摘要:
    The base catalyzed hydrophosphination reactions of (HC=CCH2PPh2)Mo(CO)(5) with Ph2PH and (Ph2PH)Mo(CO)(5) give several different products as a function of reaction conditions. These products were characterized by elemental analyses, physical properties, H-1, C-13{H-1}, and P-31{H-1} NMR spectroscopy, infrared spectroscopy, and in mast cases by X-ray crystallography.
    DOI:
    10.1016/s0022-328x(96)06599-0
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文献信息

  • Addition reactions and rearrangements of 2,3-bis(diphenylphosphino)propene and its complexes with Group 6 metal carbonyls: routes to complexes of 1,2,3-tris(diphenylphosphino)propane
    作者:Jonathan L. Bookham、William McFarlane
    DOI:10.1039/dt9900000489
    日期:——
    (1) and its Group 6 metal tetracarbonyl complexes are described. The attempted base-catalysed addition of PR2H to (1) results in rearrangement to trans-1,2-bis(diphenylphosphino)propene (2) instead of the expected triphosphine. Under the same conditions the Group 6 metal carbonyl complexes of (1) can rearrange to complexes of the cis isomer of (2), but may also undergo the addition reaction to yield
    描述了2,3-双(二苯基膦基丙烯(1)及其6族属四羰基配合物的制备。尝试的碱催化将PR 2 H加到(1)中会导致重排成反式-1,2-双(二苯基膦基丙烯(2),而不是预期的三膦。在相同条件下,(1)的第6组属羰基属配合物可以重排为(2)的顺式异构体的配合物,但也可以进行加成反应以生成M(CO)4通过调节反应条件,使新的配体1,2,3-三(二苯基膦基丙烷形成配合物。这些加热产生相应的M(CO)3配合物。介绍了新化合物的质子,13 C和31 P nmr光谱参数,并根据属和主链介导的贡献以及配位化学位移进行了讨论。
  • Synthesis and Characterization of Unsymmetrical (<i>cis</i>-(Phosphino−arsino)ethene)tetracarbonylmolybdenum Complexes: Hydroarsination Reactions of (H<sub>3</sub>CC⋮CPPh<sub>2</sub>)Mo(CO)<sub>5</sub> and [H<sub>2</sub>CCCH(DBP)]Mo(CO)<sub>5</sub> and Hydrophosphination Reactions of (Ph<sub>2</sub>AsCH<sub>2</sub>C⋮CH)Mo(CO)<sub>5</sub>
    作者:Kalyani Maitra、Vincent J. Catalano、Jerry Clark、John H. Nelson
    DOI:10.1021/ic9711170
    日期:1998.3.9
    The base-catalyzed hydroarsination reactions of (H3CC=CPPh2)Mo(CO)(5) and [H2C=C=CH(DBP)]Mo(CO)(5) (DBP=dibenzophosphole) give several different products as a function of reaction conditions. These products have been characterized by elemental analyses, physical properties, H-1, C-13H-1}, and P-31H-1} NMR spectroscopy, and, in two cases, X-ray crystallography.
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