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| 149202-05-1

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
149202-05-1
化学式
C22H18N2OP*Na
mdl
——
分子量
380.361
InChiKey
ZXPBWMLTDOGIFS-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

反应信息

  • 作为反应物:
    描述:
    bis[(benzyldimethylamino)chloropalladium(II)] 、 四氢呋喃 为溶剂, 以80%的产率得到[2-[(dimethylamino-κN)methyl]phenyl-κC]-(4-diphenylphosphino-κP-3-methyl-1-phenyl-5-pyrazolato-κO)palladium(II)*0.5benzene
    参考文献:
    名称:
    Hybrid ligands. Structure of a palladium(II) complex containing a pyrazolol-derived phosphine ligand, [(o-C6H4CH2NMe2)Pd(Ph2P{C=C(O)N(Ph)N=C(Me)})]
    摘要:
    In the title compound, {2-[(dimethylamino-kappaN)-methyl]phenyl-kappaC}(4-diphenylphosphino-kappaP-3-me-thyl-1-phenyl-5-pyrazololato-kappaO)palladium(II) 0.5-benzene solvate, [Pd(C22H18N2OP)(C9H12N)].-0.5C6H6, the Pd atom, which is in a quasi-planar environment, is complexed by two chelating three-electron-donor ligands, with P and N atoms occupying trans positions. The plane defined by the aromatic pyrazole ring is coplanar with the metal plane. The angle between the N-bonded phenyl ring and the metal plane is 8-degrees.
    DOI:
    10.1107/s010827019300664x
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文献信息

  • An Efficient Keim‐Type Catalyst Based on an Electron‐Poor <i>P</i> , <i>O</i> ‐Chelate; Tuning the Selectivity of Ethylene Oligomerisation towards Short α‐Olefins
    作者:Pierre Kuhn、David Sémeril、Catherine Jeunesse、Dominique Matt、Pierre Lutz、Richard Welter
    DOI:10.1002/ejic.200401015
    日期:2005.4
    AbstractThe tertiary phosphane Ph2P‐pzONa, in which the phosphorus atom is substituted by an electron‐withdrawing pyrazol‐onato unit, reacts with trans‐[NiPhCl(PPh3)2] to afford quan‐titatively transP,P'‐[NiPh(Ph2P‐pzO)(PPh3)] (4), the first Keim‐type catalyst derived from an amide. In the absence of any cocatalyst, complex 4 converts ethylene in high selectivity and activity into α‐olefins. The product distribution is drastically shifted towards lower oligomers when compared to the outcome of the reaction carried out with the conventional SHOP catalyst. Thus, when operating at 1 bar, over 99 wt.‐% of the oligomers formed are C4–C16 oligomers. In ethylene‐free solvents, 4 was shown to slowly undergo reductive elimination to produce the stabilised phosphorus ylide Ph3P‐pzO (5). Both compounds (4 and 5) were characterised by single‐crystal X‐ray diffraction analyses. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005)
  • Matt, Dominique; Sutter-Beydoun, Nohma; Brunette, Jean-Pierre, Inorganic Chemistry, <hi>1993</hi>, vol. 32, # 16, p. 3488 - 3492
    作者:Matt, Dominique、Sutter-Beydoun, Nohma、Brunette, Jean-Pierre、Balegroune, Fadila、Grandjean, Daniel
    DOI:——
    日期:——
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