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trans-[NiCl(CHCl2)(CN(2,6-(2,6-(i-Pr)2C6H3)2C6H3))2] | 1294005-11-0

中文名称
——
中文别名
——
英文名称
trans-[NiCl(CHCl2)(CN(2,6-(2,6-(i-Pr)2C6H3)2C6H3))2]
英文别名
——
trans-[NiCl(CHCl2)(CN(2,6-(2,6-(i-Pr)2C6H3)2C6H3))2]化学式
CAS
1294005-11-0
化学式
C63H75Cl3N2Ni
mdl
——
分子量
1025.35
InChiKey
OAAAKCVCPUOEQR-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

  • 作为产物:
    描述:
    氯仿[Ni(CN(2,6-(2,6-(i-Pr)2C6H3)2C6H3))3]乙醚 为溶剂, 以56.1%的产率得到trans-[NiCl(CHCl2)(CN(2,6-(2,6-(i-Pr)2C6H3)2C6H3))2]
    参考文献:
    名称:
    Protecting-Group-Free Access to a Three-Coordinate Nickel(0) Tris-isocyanide
    摘要:
    Details are presented regarding a convenient synthesis of the nickel trisisocyanide complex Ni(CNArDipp2)(3) (Ar-Dipp2 = 2,6-[i-Pr](2)C6H3)(2)C6H3). A previous synthesis of a Ni tris-isocyanide complex relied on a 11(I) coordination-site protection strategy to discourage the formation of a tetrakis-isocyano complex. However, protecting-group-free access to Ni(CNArr(Dipp2))3 is enabled by the encumbering m-terphenyl isocyanide CNArDipp2. Treatment of Ni(COD)2 with CNArDipp2 affords Ni(COD)(CNArDipp2)2, which is readily oxidized to NiI2(CNArDipp2)2 upon addition of I-2. Reduction of NiI2(CNArDipp2)2 with Mg metal gent:rates Ni(CNArDipp2)3 and does not require the addition of a third equivalent of CNArDipp2. Tris-isocyanide Ni(CNArDipp2)3 is active toward Lewis acid bindin)and oxidative addition reactions. Treatment of Ni(CNArDipp2)3 with TlOTf (OTf = [O3SCF3](-)) generates the salt [TINi(CNArDipp2)(3)] OTf, in which the Ni center functions as a Lewis base toward Tl. The Ni center in Ni(CNArDipp2)(3) also oxidativel adds across C-X bonds in a number of alkyl, aryl, and main-group halides and is accompanied by varying degrees of CNArDipp2 ligand loss. Formation of eta(2)-iminoacyl complexes deactivates the Ni center toward additional reactivity.
    DOI:
    10.1021/om200209w
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