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[Pt(dppe)((2,4,6-(i-Pr)3C6H2)PCH2PMe(2,4,6-(i-Pr)3C6H2))](triflate) | 1392328-68-5

中文名称
——
中文别名
——
英文名称
[Pt(dppe)((2,4,6-(i-Pr)3C6H2)PCH2PMe(2,4,6-(i-Pr)3C6H2))](triflate)
英文别名
[Pt(dppe)(meso-(isityl)PCH2PMe(isityl))](OTf);[Pt(dppe)(meso-IsPCH2PMeIs)](OTf)
[Pt(dppe)((2,4,6-(i-Pr)<sub>3</sub>C<sub>6</sub>H<sub>2</sub>)PCH<sub>2</sub>PMe(2,4,6-(i-Pr)<sub>3</sub>C<sub>6</sub>H<sub>2</sub>))](triflate)化学式
CAS
1392328-68-5
化学式
CF3O3S*C58H75P4Pt
mdl
——
分子量
1240.28
InChiKey
XOSAZKYEBKOBOS-WCSNVULCSA-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):
    15.69
  • 重原子数:
    71.0
  • 可旋转键数:
    12.0
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.39
  • 拓扑面积:
    57.2
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

反应信息

  • 作为产物:
    描述:
    2-溴-1,3,5-三异丙苯 在 lithium aluminium tetrahydride 、 sodium trimethylsilanolatemagnesium 作用下, 以 四氢呋喃乙醚二氯甲烷 为溶剂, 反应 22.0h, 生成 [Pt(dppe)((2,4,6-(i-Pr)3C6H2)PCH2PMe(2,4,6-(i-Pr)3C6H2))](triflate)
    参考文献:
    名称:
    Synthesis, Structure, Dynamics, and Selective Methylation of Platinum and Palladium Diphosphametallacyclobutane Complexes
    摘要:
    Treatment of M(dppe)Cl-2 (M = Pd, Pt) or Pt((R,R)-Me-DuPhos)Cl-2 with IsHPCH(2)PHIs (1; Is = isityl = 2,4,6-(i-Pr)(3)C6H2) and 2 equiv of NaOSiMe3 gave the mononuclear diphosphametallacyclobutane complexes M(dppe)(IsPCH(2)PIs) (M = Pd (2), Pt (3)), or Pt((1,R)-Me-DuPhos)(IsPCH(2)PIs) (4). Dynamic processes involving phosphorus inversion and rotation about the P-C (1s) bonds in 2-4 were characterized by variable-temperature NMR spectroscopy, which suggested that each existed as a single C-2-symmetric diastereomer in solution, consistent with their solid-state structures determined by X-ray crystallography. The MiniPhos derivative IsMePCH(2)PMeIs (5) was prepared as a 5.5/1 rac/meso mixture by sequential arylation and methylation of Cl2PCH2PCl2. Alternatively, the catalyst precursor Pt((1,R)-Me-DuPhos)(Ph)(Cl) mediated alkylation of secondary phosphines in the presence of NaOSiMe3 to yield selectively meso-5 either from PHMe(1s) and CH2I2 or from 1 and MeI. Recrystallization and chromatography yielded diastereomerically enriched rac-5 and meso-5. Treatment of M(dppe)(OTf)(2) (M = Pd, Pt) or Pt((R,R)-Me-DuPhos)(OTf)(2) with meso-5 gave the dications meso-[M(diphos)(IsMePCH(2)PMeIs)][OTf](2) (M(diphos) = Pd(dppe) (6), Pt(dppe) (8), Pt((R,R)-Me-DuPhos) (10)). Similar reactions of rac-5 yielded the dications rac-[M(diphos)(IsMePCH(2)PMeI(5))][OTf](2) (M(diphos) = Pd(dppe) (7), Pt(dppe) (9)) and a 1/1 mixture of the C-2-symmetric diastereomers [Pt((R,R)-Me-DuPhos)(IsMePCH(2)PMeIs)][OTf](2) (11a,b). Treatment of 2 and 3 with 2 equiv of methyl triflate gave the dications 6-9 as ca. 1/1 meso/rac mixtures, and methylation of 4 selectively gave one of the C-2-symmetric diastereomers, 11a. These alkylations proceeded via the observable monomethylated intermediates [M(diphos)(IsMePCH(2)PIs)][OTf] (12-14).
    DOI:
    10.1021/om3005367
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