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-[RhCl(CO)(PPh2(C5F4N-4))2] | 528584-61-4

中文名称
——
中文别名
——
英文名称
trans-[RhCl(CO)(PPh2(C5F4N-4))2]
英文别名
——
trans-[RhCl(CO)(PPh2(C5F4N-4))2]化学式
CAS
528584-61-4
化学式
C35H20ClF8N2OP2Rh
mdl
——
分子量
836.85
InChiKey
VPWNRUYXDLJGRU-UHFFFAOYSA-M
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:
    di(rhodium)tetracarbonyl dichloride 、 Diphenyl(tetrafluoro-4-pyridyl)phosphine二氯甲烷 为溶剂, 以82%的产率得到trans-[RhCl(CO)(PPh2(C5F4N-4))2]
    参考文献:
    名称:
    Intramolecular Dehydrofluorinative Coupling of the Asymmetric Diphosphine Ph2PCH2CH2PPh(C5F4N-4) and Pentamethylcyclopentadienyl Ligands in a Rhodium Complex
    摘要:
    The tetrafluoropyridyl-substituted diphosphine Ph2PCH2CH2PPh(C5F4N-4) (1) has been prepared in three steps from dppe. Comparison of the spectroscopic properties between trans-[RhCl(CO){PPh2(C5F4N-4)}(2)] and analogous complexes of other fluorinated triaryl phosphines reveals the lower basicity of tetrafluoropyridylphosphines relative to pentafluorophenylphosphines. The reaction between [Cp*RhCl(mu-Cl)](2) and 1 in the presence of [BF4-] yielded racemic diastereoisomers of [CP*RhCl(1)] [BF4]. In the SRhRP and RRhSP pair of enantiomers the Cp* and tetrafluoropyridyl groups have a cis disposition about the Rh-P bond, and in the SRhSP and RRhRP pair the groups are trans. In situ NMR experiments reveal that the cis pair, in which the Cp* and tetrafluoropyridyl groups are close, underwent rapid dehydrofluorinative C-C coupling to give the respective enantiomers of [{eta(5),kappaP,kappap-C5Me4CH2-2-C5F3N-4-PPhCH2-CH2PPh2}RhCl] [BF4] (6.[BF4]. The trans pair did not undergo coupling, but isomerized to the cis pair on heating in ethanol. The reaction between [Cp*RhCl(mu-Cl)](2) and 1 in refluxing benzene afforded 6.[BF4] in 64% yield after anion metathesis. The structures of OPPh2-(C5F4N-4), the cis isomer of [Cp*RhCl(1)][BF4], and one enantiomer of 6.[BF4], which crystallizes as a conglomerate, have been determined by single-crystal X-ray diffraction.
    DOI:
    10.1021/om020874p
点击查看最新优质反应信息