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trans,trans-OsCl2(η2-H2)(acetonitrile)(P(i)Pr3)2 | 1122103-70-1

中文名称
——
中文别名
——
英文名称
trans,trans-OsCl2(η2-H2)(acetonitrile)(P(i)Pr3)2
英文别名
——
trans,trans-OsCl2(η2-H2)(acetonitrile)(P(i)Pr3)2化学式
CAS
1122103-70-1;1123890-14-1
化学式
C20H47Cl2NOsP2
mdl
——
分子量
624.653
InChiKey
KRMHSSFEKYBYKB-UHFFFAOYSA-L
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:
    参考文献:
    名称:
    Behavior of OsH2Cl2(PiPr3)2 in Acetonitrile: The Importance of the Small Details
    摘要:
    The behavior of OsH2Cl2((PPr3)-Pr-i)(2) (1) in acetonitrile as solvent is studied. Acetonitrile coordinates to the metal center of 1 and promotes the dihydride-dihydrogen transformation of its OsH2 unit to give the trans-Cl-2 compound OsCl2(eta(2)-H-2)(CH3CN)((PPr3)-Pr-i)(2) (2a), which evolves to its cis-Cl-2 isomer 2b. Treatment of 1 with TlPF6 in acetonitrile leads to the PF6 salt of the cis-bis(acetonitrile) cation [OsCl(eta(2)-H-2)(CH3CN)(2)((PPr3)-Pr-i)(2)](+) (3a), which is transformed into its trans-bis(acetonitrile) isomer 3b. The addition of Et3N to the PF6 salts of 3a,b in acetonitrile gives [OsH(CH3CN)(3)((PPr3)-Pr-i)(2)]PF6 (4). Reaction of 4 with 1,5-cyclooctadiene (COD) in refluxing toluene affords [OsH(COD)(CH3CN)(2)((PPr3)-Pr-i)]PF6 (5). The X-ray structures of 3b and 5 are also reported.
    DOI:
    10.1021/om801057z
  • 作为产物:
    描述:
    bis(triisopropylphosphane)(dihydrido)dichloroosmium(IV)乙腈乙腈 为溶剂, 以72%的产率得到trans,trans-OsCl2(η2-H2)(acetonitrile)(P(i)Pr3)2
    参考文献:
    名称:
    Behavior of OsH2Cl2(PiPr3)2 in Acetonitrile: The Importance of the Small Details
    摘要:
    The behavior of OsH2Cl2((PPr3)-Pr-i)(2) (1) in acetonitrile as solvent is studied. Acetonitrile coordinates to the metal center of 1 and promotes the dihydride-dihydrogen transformation of its OsH2 unit to give the trans-Cl-2 compound OsCl2(eta(2)-H-2)(CH3CN)((PPr3)-Pr-i)(2) (2a), which evolves to its cis-Cl-2 isomer 2b. Treatment of 1 with TlPF6 in acetonitrile leads to the PF6 salt of the cis-bis(acetonitrile) cation [OsCl(eta(2)-H-2)(CH3CN)(2)((PPr3)-Pr-i)(2)](+) (3a), which is transformed into its trans-bis(acetonitrile) isomer 3b. The addition of Et3N to the PF6 salts of 3a,b in acetonitrile gives [OsH(CH3CN)(3)((PPr3)-Pr-i)(2)]PF6 (4). Reaction of 4 with 1,5-cyclooctadiene (COD) in refluxing toluene affords [OsH(COD)(CH3CN)(2)((PPr3)-Pr-i)]PF6 (5). The X-ray structures of 3b and 5 are also reported.
    DOI:
    10.1021/om801057z
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