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[Mo2Cp2(μ-H)(μ-PCy(OC6H4OH))(CO)4] | 916451-17-7

中文名称
——
中文别名
——
英文名称
[Mo2Cp2(μ-H)(μ-PCy(OC6H4OH))(CO)4]
英文别名
——
[Mo2Cp2(μ-H)(μ-PCy(OC6H4OH))(CO)4]化学式
CAS
916451-17-7
化学式
C26H27Mo2O6P
mdl
——
分子量
658.351
InChiKey
FHXKVPXAJOBIGF-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:
    [Mo2Cp2(μ-H)(μ-PCy(OC6H4OH))(CO)4]2,3,4,5,7,8,9,10-octahydropyrido[1,2-a][1,3]diazepine苯酚 在 (NH4)PF6 作用下, 以 四氢呋喃 为溶剂, 以61%的产率得到[Mo2Cp2(μ-H)(μ-PCy(OPh))(CO)4]
    参考文献:
    名称:
    Trapping of Hemiquinone Radicals at Mo and P Sites by Phosphide-Bridged Dimolybdenum Species:  Chemistry of Complexes [Mo25-C5H5)2(OC6H4OH)(μ-PR2)(CO)4] and [Mo25-C5H5)2{μ-PR(OC6H4OH)}(CO)4]- (R = Cy, Ph)
    摘要:
    The phosphide-bridged dimolybdenum complexes ( H-DBU)[ Mo2Cp2( mu-PR2)( CO)(4)] ( R) Cy, Ph; DBU) 1,8-diazabicyclo[ 5.4.0.] undec-7-ene) react with p-benzoquinone to give the hemiquinone complexes [ Mo2Cp2( OC6H4OH)( mu-PR2)( CO)(4)]. The latter experience facile homolytic cleavage of the corresponding Mo-O bonds and react readily at room temperature with HSPh or S2Ph2 to give the thiolate complexes [ Mo2Cp2( mu-PCy2)( mu-SPh)( CO)(4)] or [ Mo2Cp2( mu-PR2)( mu-SPh)( CO)(2)]. In contrast, PRH-bridged substrates experience overall insertion of quinone into the P - H bond to give the anionic compounds ( H-DBU)[ Mo2Cp2 {A- PR( OC6H4OH)}( CO)(4)], which upon acidification yield the corresponding neutral hydrides. The cyclohexyl anion experiences rapid nucleophilic displacement of the hemiquinone group by different anions ER- ( ER) OH, OMe, OC4H5, OPh, SPh) to give novel anionic compounds ( H-DBU)[ Mo2Cp2 {mu-PCy( ER)}( CO)(4)], which upon acidification yield the corresponding neutral hydrides. The structure of four of these hydride complexes [ PPh( OC6H4OH), PCy( OH), PCy( OMe), and PCy( OPh) bridges] was determined by X-ray diffraction methods and confirmed the presence of cis and trans isomers in several of these complexes. In addition, it was found that the hydroxyphosphide anion [ Mo2Cp2 {A- PCy( OH)}( CO)(4)]- displays in solution an unprecedented tautomeric equilibrium with its hydride-oxophosphinidene isomer [ Mo2Cp2( A- H) {A- PCy( O)}( CO)(4)](-).
    DOI:
    10.1021/ic061344e
  • 作为产物:
    描述:
    [Mo2(C5H5)2(μ-H)(μ-PHC6H11)(CO)4] 、 对苯醌2,3,4,5,7,8,9,10-octahydropyrido[1,2-a][1,3]diazepine 在 [NH4]PF6 作用下, 以 四氢呋喃 为溶剂, 以60%的产率得到[Mo2Cp2(μ-H)(μ-PCy(OC6H4OH))(CO)4]
    参考文献:
    名称:
    Trapping of Hemiquinone Radicals at Mo and P Sites by Phosphide-Bridged Dimolybdenum Species:  Chemistry of Complexes [Mo25-C5H5)2(OC6H4OH)(μ-PR2)(CO)4] and [Mo25-C5H5)2{μ-PR(OC6H4OH)}(CO)4]- (R = Cy, Ph)
    摘要:
    The phosphide-bridged dimolybdenum complexes ( H-DBU)[ Mo2Cp2( mu-PR2)( CO)(4)] ( R) Cy, Ph; DBU) 1,8-diazabicyclo[ 5.4.0.] undec-7-ene) react with p-benzoquinone to give the hemiquinone complexes [ Mo2Cp2( OC6H4OH)( mu-PR2)( CO)(4)]. The latter experience facile homolytic cleavage of the corresponding Mo-O bonds and react readily at room temperature with HSPh or S2Ph2 to give the thiolate complexes [ Mo2Cp2( mu-PCy2)( mu-SPh)( CO)(4)] or [ Mo2Cp2( mu-PR2)( mu-SPh)( CO)(2)]. In contrast, PRH-bridged substrates experience overall insertion of quinone into the P - H bond to give the anionic compounds ( H-DBU)[ Mo2Cp2 {A- PR( OC6H4OH)}( CO)(4)], which upon acidification yield the corresponding neutral hydrides. The cyclohexyl anion experiences rapid nucleophilic displacement of the hemiquinone group by different anions ER- ( ER) OH, OMe, OC4H5, OPh, SPh) to give novel anionic compounds ( H-DBU)[ Mo2Cp2 {mu-PCy( ER)}( CO)(4)], which upon acidification yield the corresponding neutral hydrides. The structure of four of these hydride complexes [ PPh( OC6H4OH), PCy( OH), PCy( OMe), and PCy( OPh) bridges] was determined by X-ray diffraction methods and confirmed the presence of cis and trans isomers in several of these complexes. In addition, it was found that the hydroxyphosphide anion [ Mo2Cp2 {A- PCy( OH)}( CO)(4)]- displays in solution an unprecedented tautomeric equilibrium with its hydride-oxophosphinidene isomer [ Mo2Cp2( A- H) {A- PCy( O)}( CO)(4)](-).
    DOI:
    10.1021/ic061344e
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