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| 1386955-32-3

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1386955-32-3
化学式
C31H68ClN6O2Si2Yb
mdl
——
分子量
821.584
InChiKey
JWYSATATWUELRF-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:
    描述:
    乙二醇二甲醚乙二醇二甲醚 为溶剂, 以82%的产率得到
    参考文献:
    名称:
    Syntheses of lanthanide monochloride and monoborohydride complexes supported by bridged bis(guanidinate) ligand and the use of borohydride complexes in polymerization of cyclic esters
    摘要:
    Reaction of LnCl(3) with bridged bis(guanidinate) lithium salt LLi2 (1) (L = iPr(Me3Si)NC(NiPr) N(CH2)(3)NC(NiPr)N(SiMe3)iPr) afforded the monochlorides LLnCl(THF)(2) (Ln = Nd (2), Yb (3), Y (4)) and LYbCl(DME) (5) (DME 1,2-dimethoxyethane). Complexes 2-5 were structurally characterized. Treatment of the chlorides with NaBH4 gave the monoborohydride complexes LLnBH(4)(DME) (Ln = Nd (6), Yb (7), Y (8)). X-ray crystal structure analyses of 6-8 revealed each complex was monomer with the central metal ligated by one L, one eta(3)-BH4 group and one DME. Complexes 6-8 initiate ring-opening polymerization (ROP) of epsilon-caprolactone (epsilon-CL), L-lactide (L-LA) and rac-lactide (rac-LA) as single-site initiators. The highest activity and the best molecular mass control for all the three monomers were found for the Nd system 6. The ROP of epsilon-CL in toluene with 6 gave the polymers with the (M) over bar (n exp) in good agreement with the (M) over bar (n theo) ((M) over bar (n) = the number averaged molar mass) at the molar ratio of monomer to 6 up to 600 and moderate molar mass distributions ((M) over bar (w)/(M) over bar (n) 1.43-1.52) ((M) over bar (w) the weight averaged molar mass). The ROP of L-LA with 6 in THF afforded the polymers with controlled molar mass and relatively narrow (M) over bar (w)/(M) over bar (n). Complexes 6-8 are active in the ROP of rac-LA affording poly(LA) with a slight heterotactic bias (Pr = 0.62-0.72). (C) 2012 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2012.05.011
  • 作为产物:
    描述:
    四氢呋喃氯化镱(III) 、 以 四氢呋喃 为溶剂, 以80%的产率得到
    参考文献:
    名称:
    Syntheses of lanthanide monochloride and monoborohydride complexes supported by bridged bis(guanidinate) ligand and the use of borohydride complexes in polymerization of cyclic esters
    摘要:
    Reaction of LnCl(3) with bridged bis(guanidinate) lithium salt LLi2 (1) (L = iPr(Me3Si)NC(NiPr) N(CH2)(3)NC(NiPr)N(SiMe3)iPr) afforded the monochlorides LLnCl(THF)(2) (Ln = Nd (2), Yb (3), Y (4)) and LYbCl(DME) (5) (DME 1,2-dimethoxyethane). Complexes 2-5 were structurally characterized. Treatment of the chlorides with NaBH4 gave the monoborohydride complexes LLnBH(4)(DME) (Ln = Nd (6), Yb (7), Y (8)). X-ray crystal structure analyses of 6-8 revealed each complex was monomer with the central metal ligated by one L, one eta(3)-BH4 group and one DME. Complexes 6-8 initiate ring-opening polymerization (ROP) of epsilon-caprolactone (epsilon-CL), L-lactide (L-LA) and rac-lactide (rac-LA) as single-site initiators. The highest activity and the best molecular mass control for all the three monomers were found for the Nd system 6. The ROP of epsilon-CL in toluene with 6 gave the polymers with the (M) over bar (n exp) in good agreement with the (M) over bar (n theo) ((M) over bar (n) = the number averaged molar mass) at the molar ratio of monomer to 6 up to 600 and moderate molar mass distributions ((M) over bar (w)/(M) over bar (n) 1.43-1.52) ((M) over bar (w) the weight averaged molar mass). The ROP of L-LA with 6 in THF afforded the polymers with controlled molar mass and relatively narrow (M) over bar (w)/(M) over bar (n). Complexes 6-8 are active in the ROP of rac-LA affording poly(LA) with a slight heterotactic bias (Pr = 0.62-0.72). (C) 2012 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2012.05.011
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