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[ErCl2(THF)2(((2,6-C6H3Me2)NHC(Me)CHC(Me)N(2,6-C6H3Me2))] | 1145686-48-1

中文名称
——
中文别名
——
英文名称
[ErCl2(THF)2(((2,6-C6H3Me2)NHC(Me)CHC(Me)N(2,6-C6H3Me2))]
英文别名
[ErCl2(tetrahydrofuran)2((2,6-C6H3Me2)NHC(Me)CHC(Me)N(2,6-C6H3Me2))]
[ErCl2(THF)2(((2,6-C6H3Me2)NHC(Me)CHC(Me)N(2,6-C6H3Me2))]化学式
CAS
1145686-48-1
化学式
C29H41Cl2ErN2O2
mdl
——
分子量
687.823
InChiKey
ZIZDFVXTDJDLTE-GRBIFZQPSA-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

反应信息

  • 作为产物:
    描述:
    [N(2,6-dimethylphenyl)C(Me)]2CH2 、 erbium trichloride*3.5THF 在 n-C4H9Li 作用下, 以 四氢呋喃正己烷 为溶剂, 以55.4%的产率得到[ErCl2(THF)2(((2,6-C6H3Me2)NHC(Me)CHC(Me)N(2,6-C6H3Me2))]
    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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