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| 178743-62-9

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
178743-62-9
化学式
C21H39NOsP*F6P
mdl
——
分子量
671.685
InChiKey
MBTMLXRCFWJYDP-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:
    六氟磷酸钾(η6-C6H6)OsI2(P-i-Pr3) 、 Na(1+)*ONC(CH3)C(CH3)3(1-)=NaONC(CH3)C(CH3)3 以 甲醇 为溶剂, 以67%的产率得到
    参考文献:
    名称:
    Sodium oximates as starting materials for the synthesis of half-sandwich-type arene(oximato) and arene(azavinylidene) osmium complexes
    摘要:
    The reaction of [C6H6OsI2((PPr3)-Pr-i)] (1) with Na[ON=CR(2)](R(2)=Ph(2), Me(2), C(CH2)(5)) in the presence of KPF6 leads to the formation of the oximato osmium(II) complexes [C6H6Os(eta(2)-ON=CR(2))((PPr3)-Pr-i)]PF6 (6, 7, 8b) in almost quantitative yield. The mesitylene compounds [(mes)Os(eta(2)-ON=CR'R '')(PR(3))]PF6 (9-14) have been prepared similarly using [(mes)OsCl2(PR(3))] (3-5) as starting materials. The synthesis of [C6H6Os(eta(2)-ON=CMe(t)Bu)((PPr3)-Pr-i)]PF6 (17) has been achieved from [C6H6OsCl2((PPr3)-Pr-i)] (16) which in turn is prepared from [C6H6Os(eta(2)-O2C=O)((PPr3)-Pr-i)] (15) and excess Me(3)SiCl. Reaction of 1, [C6H6OsI2(PMe(t)Bu(2))] (2) and 3 (PR(3) = (PPr3)-Pr-i) with Na[ON=CMe(t)Bu] in the presence of KPF6, in methanol as solvent, unexpectedly yields the azavinylidene complexes [(arene)Os(=N=CMe(t)Bu)(PR(3))]PF6 (18b, 19, 20). The X-ray structural analysis of 18b reveals the presence of a nearly linear Os-N-C fragment with an Os-N distance that is in agreement with typical osmium-nitrogen double bond lengths. Related azavinylideneosmium compounds [(arene)Os(=N=CR'R '')(PR(3))]PF6 (21-26) have been obtained on treatment of the corresponding oximato complexes 7, 10 or 14 with either HN=CR'R '' or, for R'=H and R ''=Ph, the trimethylsilyl derivative.
    DOI:
    10.1016/0022-328x(95)06010-t
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