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sodium bis(tetrahydrofuran) tetrakis(decafluorodiphenylamido) titanium(III) | 518026-93-2

中文名称
——
中文别名
——
英文名称
sodium bis(tetrahydrofuran) tetrakis(decafluorodiphenylamido) titanium(III)
英文别名
——
sodium bis(tetrahydrofuran) tetrakis(decafluorodiphenylamido) titanium(III)化学式
CAS
518026-93-2
化学式
C8H16NaO2*C48F40N4Ti
mdl
——
分子量
1607.57
InChiKey
JFDHTCONYMAECV-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:
    四氢呋喃四氢呋喃氯化钛1,1'-亚氨基二(2,3,4,5,6-五氟苯) 、 sodium hydride 以 四氢呋喃 为溶剂, 以15%的产率得到sodium bis(tetrahydrofuran) tetrakis(decafluorodiphenylamido) titanium(III)
    参考文献:
    名称:
    Neutral and anionic transition metal complexes supported by decafluorodiphenylamido ligands: X-ray crystal structures of {Na(THF)2}{Ti[N(C6F5)2]4}, {K(η6-C6H5Me)2}{ZrCl2[N(C6F5)2]3}, K{VCl[N(C6F5)2]3}, Fe[N(C6F5)2]2(THF)2 and Co[N(C6F5)2]2(py)2
    摘要:
    Reaction of MN(C6F5)(2) (M = Na, K) with transition metal halides results in the formation of transition metal complexes incorporating decafluorodiphenylamido ligands. TiCl3(THF)(3) reacts with 3 equiv. NaN(C6F5)(2) to yield the 'metallate' complex {Na(THF)(2)}{Ti[N(C6F5)(2)](4)} (1). Single crystal X-ray diffraction studies reveal a tetrahedral titanium center complexed by four decafluorodiphenylamido ligands; while two THF ligands and four fluorine atoms coordinate the sodium cation. ZrCl4 reacts with 3 equiv. KN(C6F5)(2) to give {K(eta(6)-C7H8)(2)}{ZrCl2[N(C6F5)(2)](3)} (2). The F-19 NMR spectrum of 2 reveals phenyl resonances in a 2:1 ratio, consistent with a trigonal bipyramidal structure being maintained in solution. The crystal structure of 2 reveals a pseudooctahedral structure, with the sixth-coordination site being completed by a weak Zr-F interaction with a pentafluorophenyl group of an amido ligand. The potassium counterion interacts in an eta(6) fashion with two toluene rings in addition to a fluorine atom arising from one of the pentafluorophenyl groups. The reaction Of VCl3 with 3 equiv. KN(C6F5)(2) generates the 'metallate' complex K{VCl[N(C6F5)(2)](3)} (3); the solid state structure of 3 reveals a distorted trigonal bipyramid with the coordination sphere being completed by a weak V-F interaction with the ortho-fluorine of one of the fluorophenyl amido ligands. Exposure of FeCl3 to 3 ;equiv. KN(C6F5)(2) results in reduction of the metal center and the formation of the Fe(II) species Fe[N(C6F5)(2)](2)(THF)(2) (4). Compound 4 is tetrahedral in the solid state with none of the weak M-F contacts observed for 1, 2, 3 and 5. COI2 reacts with 2 equiv. NaN(C6F5)(2) in the presence of pyridine to produce the expected product Co[N(C6F5)(2)](2)(py)(2) (5); X-ray crystallography reveals a five-coordinate species in the solid state which is additionally stabilized by a weak Co-F interaction. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0277-5387(02)01258-5
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