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Pt(CH2SiMe3)2(di-2-pyridyl ketone) | 1304142-81-1

中文名称
——
中文别名
——
英文名称
Pt(CH2SiMe3)2(di-2-pyridyl ketone)
英文别名
——
Pt(CH2SiMe3)2(di-2-pyridyl ketone)化学式
CAS
1304142-81-1
化学式
C19H30N2OPtSi2
mdl
——
分子量
553.711
InChiKey
LXVNPWXXYVIORG-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

  • 作为反应物:
    描述:
    Pt(CH2SiMe3)2(di-2-pyridyl ketone)碘甲烷丙酮 为溶剂, 以64%的产率得到cis-PtI(Me)(CH2SiMe3)2(di-2-pyridyl ketone)
    参考文献:
    名称:
    Trimethylsilylplatinum(IV) complexes as reaction intermediates
    摘要:
    The oxidative addition of I-2, PhCH2Br and MeI with [Pt(CH2SiMe3)(2)(DPK)], 1, DPK = di-2-pyridyl ketone, occurred with trans stereochemistry to give [PtI2(CH2SiMe3)(2)(DPK)], [PtBr(CH2Ph)(CH2SiMe3)(2)(DPK)] and [PtIMe(CH2SiMe3)(2)(DPK)], respectively. Complex 1 reacted with acids HX (X = Cl or CF3CO2) to give initially the hydridoplatinum complexes [PtHX(CH2SiMe3)(2)(DPK)], but these complexes were thermally unstable and decomposed largely by alpha-silyl migration to give compounds such as [PtX(SiMe3)Me-2(DPK)], as determined by monitoring the reactions by NMR at low temperature. With excess acid, HX, at room temperature, the products were largely [PtX2(DPK)], CH4 and Me3SiX with Me4Si as a minor product only. The mechanism of the easy Si-CH2 bond cleavage is discussed. (C) 2010 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.ica.2010.11.018
  • 作为产物:
    描述:
    2-二吡啶基酮 、 Pt2(CH2SiMe3)4(.mi.-SMe2)2 以 乙醚 为溶剂, 以74%的产率得到Pt(CH2SiMe3)2(di-2-pyridyl ketone)
    参考文献:
    名称:
    Trimethylsilylplatinum(IV) complexes as reaction intermediates
    摘要:
    The oxidative addition of I-2, PhCH2Br and MeI with [Pt(CH2SiMe3)(2)(DPK)], 1, DPK = di-2-pyridyl ketone, occurred with trans stereochemistry to give [PtI2(CH2SiMe3)(2)(DPK)], [PtBr(CH2Ph)(CH2SiMe3)(2)(DPK)] and [PtIMe(CH2SiMe3)(2)(DPK)], respectively. Complex 1 reacted with acids HX (X = Cl or CF3CO2) to give initially the hydridoplatinum complexes [PtHX(CH2SiMe3)(2)(DPK)], but these complexes were thermally unstable and decomposed largely by alpha-silyl migration to give compounds such as [PtX(SiMe3)Me-2(DPK)], as determined by monitoring the reactions by NMR at low temperature. With excess acid, HX, at room temperature, the products were largely [PtX2(DPK)], CH4 and Me3SiX with Me4Si as a minor product only. The mechanism of the easy Si-CH2 bond cleavage is discussed. (C) 2010 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.ica.2010.11.018
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