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(C5Me5)2Y[iPrNC(H)NiPr-κ2N,N′] | 1392226-64-0

中文名称
——
中文别名
——
英文名称
(C5Me5)2Y[iPrNC(H)NiPr-κ2N,N′]
英文别名
——
(C<sub>5</sub>Me<sub>5</sub>)<sub>2</sub>Y[<sup>i</sup>PrNC(H)N<sup>i</sup>Pr-κ<sup>2</sup>N,N′]化学式
CAS
1392226-64-0
化学式
C27H45N2Y
mdl
——
分子量
486.574
InChiKey
XMGCGPQJWYRVHX-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:
    (C5Me5)2Y(μ-H)YH(C5Me5)2N,N'-二异丙基碳二亚胺甲基环己烷 为溶剂, 以99%的产率得到(C5Me5)2Y[iPrNC(H)NiPr-κ2N,N′]
    参考文献:
    名称:
    Reactivity of the Y3+ Tuck-Over Hydride Complex, (C5Me5)2Y(μ-H)(μ-CH2C5Me4)Y(C5Me5)
    摘要:
    The trivalent yttrium tuck-over hydride complex, (C5Me5)(2)Y(mu-H)(mu-eta(1):eta(5)-CH2C5Me4)Y(C5Me5), 1, acts as a reductant in reactions in which the (mu-H)(-) hydride ligand and the bridging Y-C alkyl anion linkage in the mu-eta(1):eta(5)-CH2C5Me4)(2-) ligand combine to form a C-H bond in (C5Me5)(-) and deliver two electrons to a substrate. Complex 1 reacts with PhSSPh, AgOTf (OTf = OSO2CF3), and Et3NHBPh4 to form [(C5Me5)(2)Y(mu-SPh)](2), [(C5Me5)(2)Y(mu-OTf)](2), and (C5Me5)(2)Y(mu-Ph)(2)BPh2, respectively. The reactivity of the Y-H and Y-CH2C5Me4 linkages in 1 was probed via carbodiimide insertion reactions. (PrN)-Pr-i=C=(NPr)-Pr-i inserts into both Y-H and Y-C bonds to yield (C5Me5)[(PrNC)-Pr-i(H)(NPr)-Pr-i]Y{mu-eta(5)-C5Me4CH2[(PrNCNPr)-Pr-i-Pr-i]}Y(C5Me5)(2). Carbodiimide insertion with [(C5Me5)(2)YH](2), 2, was also examined for comparison, and (C5Me5)(2)Y[(PrNC)-Pr-i(H)(NPr)-Pr-i-kappa N-2,N'] was isolated and structurally characterized. To examine the possibility of selective reactivity of the bridging ligands, mu-H versus mu-CH2C5Me4, trimethylsilylchloride was reacted with 1, and the tuck-over chloride complex, (C5Me5)(2)Y(mu-Cl)(mu-eta(1):eta(5)-CH2C5Me4)Y(C5Me5), was isolated.
    DOI:
    10.1021/om300546t
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