摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

trans-[Os(H)(N2)(1,2-bis(diphenylphosphino)ethane)2]BF4 | 203581-72-0

中文名称
——
中文别名
——
英文名称
trans-[Os(H)(N2)(1,2-bis(diphenylphosphino)ethane)2]BF4
英文别名
——
trans-[Os(H)(N2)(1,2-bis(diphenylphosphino)ethane)2]BF4化学式
CAS
203581-72-0
化学式
BF4*C52H49N2OsP4
mdl
——
分子量
1102.87
InChiKey
ITANIKPZPVXNAU-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

  • 作为产物:
    描述:
    二氯甲烷 、 trans-[Os(H)(SPh)(1,2-bis(diphenylphosphino)ethane)2]BF4 、 二氯甲烷 为溶剂, 生成 [Os(H)(H2)(1,2-bis(diphenylphosphino)ethane)2](1+) 、 Os(H)Cl(1,2-bis(diphenylphosphino)ethane)2 、 trans-[Os(H)(N2)(1,2-bis(diphenylphosphino)ethane)2]BF4
    参考文献:
    名称:
    Protonation Reactions of trans-M(H)(SPh)(dppe)2 (M = Ru, Os) To Give Thiol and Dihydrogen Complexes. X-ray Crystal Structure Determination of trans-Ru(H)(SPh)(dppe)2 and trans-[Os(H)(O2)(dppe)2](O3SCF3)
    摘要:
    The compounds trans-M(H)(SPh)(dppe)(2) (M = Ru (1Ru), Os (1Os); dppe = 1,2-bis(diphenylphosphino)ethane) are synthesized by reaction of NaSPh with trans-[Ru(H-2)(H)(dppe)(2)]BPh4 or with trans-Os(H)(Br)(dppe)2 in THF under Ar. They are characterized by H-1 and P-31 NMR, IR, FAB mass spectroscopy, elemental analyses, and cyclic voltammetry. The crystal structure determination of 1Ru verifies the trans, octahedral geometry, which is distorted by ring-ring interactions. The thiophenoxide ligand is coordinated to the metal in a bent configuration, with the phenyl ring sandwiched between two phenyl rings of one of the dppe ligands. The reaction of complexes 1 with 1 equiv of HBF4 . Et2O leads to the formation of the very reactive hydride thiol complexes trans-[M(H)-(HSPh)(dppe)(2)]BF4 (M = Ru (2Ru), Os (2Os)). Analogous complexes to 1Os and 2Os with SC6H4-4-F -F instead of SPh are also described. In all cases there is no evidence for the existence of the tautomeric dihydrogen complex trans-[M(H-2)(SAr)(dppe)(2)](+). Zn the presence of excess acid the diprotonated complex trans-[Os(H-2)(HSPh)-(dppe)(2)](BF4)(2) (3Os) is formed at 233 K where the T-1(min) of the H-2 ligand at 400 MHz is similar to 34 ms so that 0.98 less than or equal to d(HH) less than or equal to 1.24 Angstrom. Under certain conditions the labile PhSH ligand of 3Os is substituted by water to give trans[Os(H-2)(OH2)(dppe)(2)](BF4)2 (4OS). The thiol complexes 2 react rapidly with H-2(g) to give the complexes trans[M(H-2)H(dppe)(2)]BF4 (5Ru, 5Os). Complexes 3Os and 4Os also react with H-2 to give 5Os. N-2 and O-2(1 atm) displace the thiol in 2Os in CH2Cl2 to produce trans-[Os(H)(L)(dppe)(2)](+) (L eta(1)-N-2 (6Os), eta 2-O-2(7OS)). trans[Os(H)(O-2)(dppe)(2)]OTf . 3C(6)H(6) is characterized by X-ray diffraction.
    DOI:
    10.1021/ic971050g
点击查看最新优质反应信息