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[2-MeOC6H4NC(tBu)N(C6H3-iPr2-2,6)]YbN(SiMe3)2(THF) | 1535208-06-0

中文名称
——
中文别名
——
英文名称
[2-MeOC6H4NC(tBu)N(C6H3-iPr2-2,6)]YbN(SiMe3)2(THF)
英文别名
——
[2-MeOC<sub>6</sub>H<sub>4</sub>NC(tBu)N(C<sub>6</sub>H<sub>3</sub>-iPr<sub>2</sub>-2,6)]YbN(SiMe<sub>3</sub>)<sub>2</sub>(THF)化学式
CAS
1535208-06-0
化学式
C34H59N3O2Si2Yb
mdl
——
分子量
771.072
InChiKey
XVPIPTOEFLUTIF-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

  • 作为产物:
    描述:
    bis[N,N-bistrimethylsilylamido]bis(tetrahydrofuran)ytterbium(II) 、 以 甲苯 为溶剂, 反应 1.0h, 以78%的产率得到[2-MeOC6H4NC(tBu)N(C6H3-iPr2-2,6)]YbN(SiMe3)2(THF)
    参考文献:
    名称:
    Divalent Heteroleptic Ytterbium Complexes – Effective Catalysts for Intermolecular Styrene Hydrophosphination and Hydroamination
    摘要:
    New heteroleptic Yb(II)-amide species supported by amidinate and 1,3,6,8-tetra-tert-butylcarbazol-9-yl ligands [2-MeOC6H4NC(tBu)N-(C6H3-iPr(2)-2,6)]YbN(SiMe3)(2)(THF) (6) and [1,3,6,8-tBu(4)C(12)H(4)N]Yb[N(SiMe3)(2)](THF)(n) (n = 1 (7), 2 (8)) were synthesized using the amine elimination approach. Complex 6 features an unusual kappa(1)-N,kappa(2)-O,eta(6)-arene coordination mode of the amidinate ligand onto Yb(II). Complexes 7 and 8 represent the first examples of lanthanide complexes with pi-coordination of carbazol-9-yl ligands. Complexes 6 and 7, as well as the amidinate-Yb(II)-amide [tBuC(NC6H3-iPr(2)-2,6)(2)]YbN(SiMe3)(2)(THF) (5), are efficient pre-catalysts for the intermolecular hydrophosphination and hydroamination of styrene with diphenylphosphine, phenylphosphine, and pyrrolidine to give exclusively the anti-Markovnikov monoaddition product. For both types of reaction, the best performances were observed with carbazol-9-yl complex 7 (TONs up to 92 and 48 mol/mol at 60 degrees C, respectively).
    DOI:
    10.1021/ic4027859
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