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[PdCl(η3-2-CH3-C3H4)(2-pyridyldiphenylphosphine(+1H))][CH3SO3] | 1105613-74-8

中文名称
——
中文别名
——
英文名称
[PdCl(η3-2-CH3-C3H4)(2-pyridyldiphenylphosphine(+1H))][CH3SO3]
英文别名
——
[PdCl(η3-2-CH3-C3H4)(2-pyridyldiphenylphosphine(+1H))][CH3SO3]化学式
CAS
1105613-74-8
化学式
CH3O3S*C21H22ClNPPd
mdl
——
分子量
556.358
InChiKey
XBTLBKSABDIJFN-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:
    参考文献:
    名称:
    Protonation of palladium(II)-allyl and palladium(0)-olefin complexes containing 2-pyridyldiphenylphosphine
    摘要:
    The pendant nitrogen atom of the Ph2PPy ligand in the Pd(II)-allyl complexes [PdCl(eta(3)-2-CH3C3H4)( Ph2PPy)] (1) and [Pd(eta(3)-2-CH3-C3H4)(Ph2PPy)(2)]BF4 (3) has been protonated with methanesulfonic acid to afford the corresponding pyridinium salts [PdCl(eta(3)-2-CH3-C3H4)(Ph2PPyH)](CH3SO3) (1a) and [Pd(eta(3)-2-CH3-C3H4)(Ph2PPyH)(2)](CH3SO3)(2)(BF4) (3a).Protonation strongly influences the H-1 and C-13 NMR spectral parameters of the allyl moieties of 1a and 3a whose signals resonate at lower fields with respect to the parent species indicating that upon protonation Ph2PPy becomes a weaker sigma-donor and a stronger Pi-acceptor. The allyl moiety, which in 1 is static, becomes dynamic in 1a, the observed syn-syn and anti-anti exchange being due to deligation of the protonated phosphine from the metal centre. Treatment of complex 3 with diethylamine in the presence of fumaronitrile gives the new Pd(0)-olefin complex [Pd(eta(2)-fumaronitrile)(PPh2Py)(2)] (4) which has been characterized by elemental analysis and NMR spectroscopy. Low temperature protonation of 4 with methanesulfonic acid leads to the bis-protonated species [Pd(eta(2)-fumaronitrile)(Ph2PPyH)(2)](CH3SO3)(2) (4a) which is stable only at temperatures < 0 degrees C. (C) 2008 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2008.09.063
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