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[((2,6-C6H3Et2)NHC(Me)CHC(Me)N(2,6-C6H3Et2))Gd3Cl3(THF)2][B(C6F5)4]] | 1225638-47-0

中文名称
——
中文别名
——
英文名称
[((2,6-C6H3Et2)NHC(Me)CHC(Me)N(2,6-C6H3Et2))Gd3Cl3(THF)2][B(C6F5)4]]
英文别名
[((2,6-C6H3Et2)NHC(Me)CHC(Me)N(2,6-C6H3Et2))2Gd2Cl3(tetrahydrofuran)2][B(C6F5)4]
[((2,6-C6H3Et2)NHC(Me)CHC(Me)N(2,6-C6H3Et2))Gd3Cl3(THF)2][B(C6F5)4]]化学式
CAS
1225638-47-0
化学式
C24BF20*C58H82Cl3Gd2N4O2
mdl
——
分子量
1967.22
InChiKey
JHENKCRVNGOATL-QDTPVHQTSA-K
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

  • 作为产物:
    描述:
    [GdCl2(THF)2(((2,6-C6H3Et2)NHC(Me)CHC(Me)N(2,6-C6H3Et2))]三苯碳四(五氟苯基)硼酸盐 在 isoprene 、 Al(CH3)3 作用下, 以 甲苯 为溶剂, 以38%的产率得到[((2,6-C6H3Et2)NHC(Me)CHC(Me)N(2,6-C6H3Et2))Gd3Cl3(THF)2][B(C6F5)4]]
    参考文献:
    名称:
    β-Diketiminato Rare-Earth Metal Complexes. Structures, Catalysis, and Active Species for Highly cis-1,4-Selective Polymerization of Isoprene
    摘要:
    Lithiation of the beta-diketimines (2,6-C6H3R2)NH=C(Me)CH=C(Me)N(2,6-C6H3R2) (R = Me (HL1), Et (HL2)) by nBuLi was followed by metathesis reaction with LnCl(3)(THF)(x) and Y(BH4)(3)(THF)(2) to afford the corresponding complexes L(1)LnCl(2)(THF)(2) (Ln = Gd (1), Nd (3), Dy (4), Er (5), Y (6)), (LGdCl2)-Gd-2(THF)2 (2), and (LY)-Y-1(BH4)(2)(THF) (8), respectively. Treatment of neutral HL1 with Y(CH2SiMe3)(3)(THF)(2) generated the bis(alkyl) complex 7, (LY)-Y-1(CH2SiMe3)(2)-(THF). Upon activation with [PhNHMe2][B(C6F5)(4)] and AliBu(3), complex 6 showed the highest cis1,4 selectivity (99.3%, T-p = 0 degrees C) toward the polymerization of isoprene, while complex 7 had a comparatively low cis-1,4 selectivity, and in contrast, complex 8 was completely inert. The influences of the ortho substituents of the N-aryl rings of the ligands, the types of central metals and cocatalysts, and addition sequence of the catalyst components had been thoroughly investigated. By means of X-ray diffraction and H-1 NMR spectroscopy analyses, the intermediates arising from the stoichiometric reactions among the catalyst components and the probable active species were elucidated, which facilitates further investigation of the mechanism for diene polymerization.
    DOI:
    10.1021/om100100r
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