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| 176112-54-2

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
176112-54-2
化学式
C41H37ClO2P3Pt*F6P
mdl
——
分子量
1030.16
InChiKey
MQAPWPDGYUSUFW-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:
    一氧化碳四氢呋喃氘代乙腈 为溶剂, 生成
    参考文献:
    名称:
    Reactivity of Platinum−Oxygen Bonds:  Kinetic and Mechanistic Studies of the Carbonylation of Platinum Aryloxide Complexes and the Formation of (Aryloxy)carbonyls
    摘要:
    The reactions of [Pt(triphos)(Cl)][Cl] (1) {triphos = bis[2-diphenylphosphino)ethyl]phenylphosphine} with NaOC6H4-p-R, in the presence of NaPF6, yields the aryloxy complexes [Pt(triphos)(OC6H4-p-R)][PF6] (R = OMe (2a), Me (2b), H (2c), F (2d), Cl (2e)). Upon reaction of 2a-e with carbon monoxide at pressures from 10 to 134 psi in acetonitrile the (aryloxy)carbonyl complexes [Pt(triphos)C(O)OC6H4-p-R)][PF6] (3a-e) were obtained. The molecular structure of [Pt(triphos)(C(O)OC6H4-p-Me)][PF6] (3b) was determined by X-ray diffraction. Complex 3b crystallized in the monoclinic space group P2(1)/n (no. 14) with a = 10.797(1) Angstrom, b = 19.927(3) Angstrom, c = 19.113(2) Angstrom, beta = 98.07(1)degrees, V = 4071(2) Angstrom(3), and Z = 4. The structure was solved and refined to R = 0.035 and R(w) = 0.040 for 3958 reflections with I > 3 sigma(I). The kinetics of the carbonylation of 2a-e to form 3a-e were studied by P-31{H-1} NMR. Rates of carbonylation exhibit a first order dependence on [CO], but are independent of the concentration of free aryloxide in solution. Rates of aryloxide ligand exchange were also found to be significantly faster than rates of carbonylation. The rates of carbonylation depend on the para-substituent of the aryloxy ligand and follow the order F (2d) > Me (2b) > OMe (2a). These observations are interpreted in terms of a carbonylation mechanism that proceeds via a migratory insertion pathway, rather than by nucleophilic attack at coordinated carbon monoxide by free or dissociated aryloxide.
    DOI:
    10.1021/ja952680p
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