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[PdClMe(1-CH2P(4-OCH3C6H4)2-4-CH2P(3-CF3C6H4)2-C6H4)] | 917392-79-1

中文名称
——
中文别名
——
英文名称
[PdClMe(1-CH2P(4-OCH3C6H4)2-4-CH2P(3-CF3C6H4)2-C6H4)]
英文别名
[Pd(1-[bis(3-trifluoromethyl)phosphinomethyl]-2-[bis(4-methoxyphenyl)phosphinomethyl]benzene)Cl(CH3)]
[PdClMe(1-CH2P(4-OCH3C6H4)2-4-CH2P(3-CF3C6H4)2-C6H4)]化学式
CAS
917392-79-1
化学式
C37H33ClF6O2P2Pd
mdl
——
分子量
827.479
InChiKey
NGGQTSSCBZOTRW-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

  • 作为反应物:
    参考文献:
    名称:
    Carbonylation studies of Pd-methyl complexes modified with 1,4-Cs-symmetrical diphosphine ligands
    摘要:
    Neutral palladium methyl chloride 2a-d [PdCH3((PP)-P-boolean AND')Cl] and cationic palladium methyl acetonitrile mono-triflate 3a-d [PdCH3((PP)-P-boolean AND')(CH3CN)](CF3SO3).complexes were synthesized and fully characterized ((PP)-P-boolean AND' = 1a-d). All the neutral and cationic complexes containing a C-s-symmetric diphosphine exist in solution as a mixture of geometric isomers. The carbonylation at atmospheric pressure of the neutral and cationic complexes revealed that migratory insertion of carbon monoxide is not stereospecific in these systems. The neutral and cationic acyl complexes were formed in situ as mixtures of stereoisomers, which were characterized by means of NMR spectroscopy.The crystal structures of [Pd(1a)Cl](2)(OTf)(2) and 2d are described. (c) 2006 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2006.06.038
  • 作为产物:
    描述:
    chloromethyl(1,5-cyclooctadiene)palladium(II) 、 1-CH2P(4-OCH3C6H4)2-4-CH2P(3-CF3C6H4)2-C6H4二氯甲烷 为溶剂, 以91%的产率得到[PdClMe(1-CH2P(4-OCH3C6H4)2-4-CH2P(3-CF3C6H4)2-C6H4)]
    参考文献:
    名称:
    Carbonylation studies of Pd-methyl complexes modified with 1,4-Cs-symmetrical diphosphine ligands
    摘要:
    Neutral palladium methyl chloride 2a-d [PdCH3((PP)-P-boolean AND')Cl] and cationic palladium methyl acetonitrile mono-triflate 3a-d [PdCH3((PP)-P-boolean AND')(CH3CN)](CF3SO3).complexes were synthesized and fully characterized ((PP)-P-boolean AND' = 1a-d). All the neutral and cationic complexes containing a C-s-symmetric diphosphine exist in solution as a mixture of geometric isomers. The carbonylation at atmospheric pressure of the neutral and cationic complexes revealed that migratory insertion of carbon monoxide is not stereospecific in these systems. The neutral and cationic acyl complexes were formed in situ as mixtures of stereoisomers, which were characterized by means of NMR spectroscopy.The crystal structures of [Pd(1a)Cl](2)(OTf)(2) and 2d are described. (c) 2006 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2006.06.038
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文献信息

  • NovelCs-Symmetric 1,4-Diphosphine Ligands in the Copolymerization of Propene and Carbon Monoxide: High Regio- and Stereocontrol in the Catalytic Performance
    作者:Antonella Leone、Giambattista Consiglio
    DOI:10.1002/hlca.200590002
    日期:2005.2
    New Cs-symmetric aryl 1,4-diphosphine ligands were synthesized and tested in the copolymerization of carbon monoxide and propene. The electronic properties of the two different P-atoms did not affect the high enantioselectivity of the catalyst precursors, thus resulting in high ‘regio’- and ‘stereoregular’ copolymers.
    新Ç小号-对称芳1,4-二膦配体的合成和在一氧化碳丙烯的共聚合进行试验。两种不同的P原子的电子特性不会影响催化剂前体的高对映选择性,因此会产生高“区域”和“立体规则”共聚物。
  • High-pressure NMR study of migratory CO-insertion in palladium–methyl complexes modified with Cs-symmetrical 1,4-diphosphines
    作者:Antonella Leone、Sebastian Gischig、Cornelis J. Elsevier、Giambattista Consiglio
    DOI:10.1016/j.jorganchem.2007.01.020
    日期:2007.4
    Carbonylation of the palladium complexes [PdCH3((PP)-P-boolean AND')Cl] ((PP)-P-boolean AND'= 1a, 1b, 1c, 1d, 1e) and [PdCH3((PP)-P-boolean AND')(CH3CN)](OTf) was investigated by means of high-pressure NMR with the determination of the half-life times t(1/2). The results were rationalized on the basis of the electronic properties of the diphosphines and the nature of the solvento ligand in the first coordination sphere. The crystal structures of the complexes [Pd(1b)Cl-2] and [Pd(1b)(H2O)(2)](OTf)(2) are described (1b = 1-(diphenylphosphinomethyl)-2-[bis(3- trifluoromethylphenyl)phosphinomethyl]benzene). (c) 2007 Elsevier B.V. All rights reserved.
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