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[PdCl2(Me2NCN){N=C(NMe2)ON(C6H4Cl-p)CPh2}] | 1403456-44-9

中文名称
——
中文别名
——
英文名称
[PdCl2(Me2NCN){N=C(NMe2)ON(C6H4Cl-p)CPh2}]
英文别名
——
[PdCl<sub>2</sub>(Me<sub>2</sub>NCN){N=C(NMe<sub>2</sub>)ON(C<sub>6</sub>H<sub>4</sub>Cl-p)CPh<sub>2</sub>}]化学式
CAS
1403456-44-9
化学式
C25H26Cl3N5OPd
mdl
——
分子量
625.293
InChiKey
PCKZRVLMMNCBPQ-UHFFFAOYSA-L
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:
    参考文献:
    名称:
    A Palladium(II) Center Activates Nitrile Ligands toward 1,3-Dipolar Cycloaddition of Nitrones Substantially More than the Corresponding Platinum(II) Center
    摘要:
    Palladium(II)-coordinated NCR1 (R-1 = Et (1), NMe2 (2), Ph (3)) species react smoothly with acyclic nitrones such as the ketonitrones Ph2C=N(O)R-4 (R-4 = p-MeC6H4 (4), p-ClC6H4 (5)) and the aldonitrone p-MeC6H4CH=N(O)Me (6) in the corresponding nitrile media. This reaction proceeds as a consecutive two-step intermolecular cycloaddition to give the mono- and bis-2,3-dihydro-1,2,4-oxadiazole complexes [PdCl2((RCN)-C-1){N-a=C (R-1) ON (R-4)C-b((RR3)-R-2)}}((a-b)) (7a-13a; R-2, R-3 = Ph; R-4 = C6H4Me-p, R-1 = Et (7), NMe2 (8), Ph (9); R4 = C6H4C1-p, = Et (10), NMe2 (11), Ph (12); R2 = H, R-3 = C6H4Me-p, R-4 = Me, R-1 = NMe2 (13)) and [PdCl2{Na= C(R-1)ON(R-4)Cb((RR3)-R-2)}(2)]((a-b)) (7b-13b), respectively. Inspection of the obtained data and their comparison with the previous results indicate that the Pd-II centers provide substantially greater activation of RCN ligands toward the 1,3-dipolar cycloaddition than the relevant Pt-II centers. The palladium(II)-mediated 1,3-dipolar cycloaddition of ketonitrones to nitriles is reversible. All complexes were characterized by elemental analyses (C, H, N), high-resolution ESI-MS, and IR and H-1 and C-13{H-1} NMR spectroscopy. The structure of trans7b was determined by single-crystal X-ray diffraction. Metal-free 5-NR'2-2,3-dihydro-1,2,4-oxadiazoles (7c-13c) were liberated from the corresponding (2,3-dihydro-1,2,4-oxadiazole)2Pd(II) complexes by treatment with 1,2-(diphenylphosphino)ethane, and the heterocycles were characterized by high-resolution ESI+-MS and H-1 and 13C{IFI} spectroscopy.
    DOI:
    10.1021/ic301866y
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