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[N(CH2CH2NHC6F5)3]V=N(3,5-Me2C6H3) | 177778-09-5

中文名称
——
中文别名
——
英文名称
[N(CH2CH2NHC6F5)3]V=N(3,5-Me2C6H3)
英文别名
——
[N(CH2CH2NHC6F5)3]V=N(3,5-Me2C6H3)化学式
CAS
177778-09-5
化学式
C8H9N*C24H12F15N4*V
mdl
——
分子量
811.47
InChiKey
OCODOEPYZKTVDO-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):
    11.26
  • 重原子数:
    53.0
  • 可旋转键数:
    12.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    67.84
  • 氢给体数:
    0.0
  • 氢受体数:
    1.0

反应信息

  • 作为产物:
    描述:
    3,5-二甲基苯基异氰酸酯间二甲苯 为溶剂, 以47%的产率得到[N(CH2CH2NHC6F5)3]V=N(3,5-Me2C6H3)
    参考文献:
    名称:
    Synthesis of Vanadium(III), -(IV), and -(V) Complexes That Contain the Pentafluorophenyl-Substituted Triamidoamine Ligand [(C6F5NCH2CH2)3N]3-
    摘要:
    [N3N]V=O ([N3N](3-) = [(C6F5NCH2CH2)(3)N](3-)) was prepared from VOCl3 and H-3[N3N] in the presence of Et(3)N. Related arylimido complexes, [N3N]V=NAr (Ar = p-MeC(6)H(4), p-CF3C6H4, or p-FC6H4), were prepared in high yields from the known V(NAr)Cl-3(THF) complexes in a similar manner or by treating [N3N]V=O with an aryl isocyanate in refluxing m-xylene. New imido complexes also were prepared by reacting an imido complex with an aryl isocyanate over a period of 2 days in refluxing mesitylene. The reaction between VCl3(THF)(3) and H-3[N3N] in the presence of triethylamine gave [HNEt(3)]{[N3N]VCl} (3) when the reaction was carried out in ether and [N3N]V(CH3CN) (4a) when carried out in acetonitrile, while the reaction between VCl3(THF)(3) and H-3[N3N] in the presence of triethylamine and tert-butyl isocyanide gave green [N3N]V(t-BuNC). [N3N]V(CH3CN) reacts with propylene oxide to give [N3N]V=O and with diazoalkanes to give [N3N]V=NN=CHR (R = SiMe(3), CO2C2H5). An X-ray structure determination of 4a (C26H15N5F15V, a = 13.021(1) Angstrom, b = 13.021(1) Angstrom, c = 14.221(1) Angstrom, gamma = 120 degrees, rhombohedral, R3 (h), Z = 3) shows it to be a pseudo-trigonal-bipyramidal species with acetonitrile coordinated in the apical position. An attempt to prepare the iodo analog of 3 by adding Me(3)SiI in THF to it yielded green crystalline [N3N]V(THF) (5). An X-ray structure determination of 5 (C28H20N4F15OV, a = 15.390(7) Angstrom, b = 12.189(6) Angstrom, c = 16.368(7) Angstrom, beta = 109.96 (3)degrees, monoclinic, P2(1)/n, Z = 4) shows it to be a pseudo trigonal bipyramid containing 1 equiv of THF in the axial position in a structure that otherwise is similar to that of 4a. [HNEt(3)]{[N3N]VCl} reacts with ferrocenium triflate to yield [N3N]VCl, a species that can be reduced to 5 in THF by sodium amalgam.
    DOI:
    10.1021/ic951433j
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