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(thf)3Li(N,N-bis-(diphenylphosphino)amine) | 181944-94-5

中文名称
——
中文别名
——
英文名称
(thf)3Li(N,N-bis-(diphenylphosphino)amine)
英文别名
(tetrahydrofuran)3lithium bis(diphenylphosphino)amide;(THF)3Li(N(PPh2)2;lithium;bis(diphenylphosphanyl)azanide;oxolane
(thf)3Li(N,N-bis-(diphenylphosphino)amine)化学式
CAS
181944-94-5
化学式
C36H44LiNO3P2
mdl
——
分子量
607.639
InChiKey
QOCDCVYZDUUXMB-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

  • 作为反应物:
    参考文献:
    名称:
    Synthesis and structures of diphosphinoamide complexes of nickel, palladium and platinum
    摘要:
    Lithium bis(diphenylphosphino)amide, (THF)(3)LiN(PPh2)(2) reacts with Ni(COD)(2) or PtMe2(COD) to give the corresponding bimetallic complexes (THF)(3)LiN(PPh2)(2)Ni(COD) and (THF)(3)LiN(PPh2)(2)PtMe2. Reaction of (THF)(3)LiN(PPh2)(2)Ni(COD) with Me3SnCl gave the Ni-Sn derivative, also accessible from Me3SnN(PPh2)(2). The silyl derivatives Me3SiN(PPh2)(2)M [M = Ni(COD), PtMe2] were obtained similarly as red and colourless crystals, respectively. By contrast, the reaction with PdCl2(COD) afforded an insoluble yellow adduct which, on attempted recrystallisation afforded a small amount of a Pd(I) product, [PdCl{HN(PPh2)(2)}](2). The crystal structures of the Ni and Pt complexes are based on MP2N four-membered rings. The geometric parameters proved rather insensitive to changes in the N-main group element bond. In all cases the amido-nitrogen atom deviated slightly from trigonal-planar geometry, most probably as the consequence of packing forces. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2005.07.027
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文献信息

  • Highly Strained Heterometallacycles of Group 4 Metallocenes with Bis(diphenylphosphino)amide Ligands
    作者:Martin Haehnel、Sven Hansen、Anke Spannenberg、Perdita Arndt、Torsten Beweries、Uwe Rosenthal
    DOI:10.1002/chem.201201114
    日期:2012.8.20
    A study regarding coordination chemistry of the bis(diphenylphosphino)amide ligand Ph2P‐N‐PPh2 at Group4 metallocenes is presented herein. Coordination of N,N‐bis(diphenylphosphino)amine (1) to [(Cp2TiCl)2] (Cp=η5‐cyclopentadienyl) generated [Cp2Ti(Cl)P(Ph2)N(H)PPh2] (2). The heterometallacyclic complex [Cp2Ti(κ2‐P,P‐Ph2P‐N‐PPh2)] (3 Ti) can be prepared by reaction of 2 with n‐butyllithium as well
    本文介绍了有关第4组茂属上双(二苯基膦基)酰胺配体Ph 2 P-N-PPh 2的配位化学的研究。的协调N,N-双(二苯基膦基)胺(1)至[(CP 2的TiCl)2 ](CP =η 5 -环戊二烯基)中产生的[CP 2的Ti(Cl)的P(博士2)N(H)PPH 2 ](2)。所述heterometallacyclic复杂的[CP 2的Ti(κ 2 - P,P -Ph 2 P-N-PPH 2)](3的Ti)可以通过反应来制备2与Ñ丁基以及从该反应的已知二茂-炔复合物的[CP 2的Ti(η 2 -Me 3的SiC 2森达3)]与胺1。酰胺[(thf)3 Li N(PPh 2)2 }]与[CP 2 MCl 2 ](M = Zr,Hf)的反应产生相应的茂和ha茂属配合物[CP 2 M(Cl)κ 2 ‐ N,P ‐N(PPh 2)2 }](4 Zr和4 Hf)。的还原4 Zr的,得到
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