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| 262854-89-7

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
262854-89-7
化学式
CF3O3S*C34H30F15MoN6
mdl
——
分子量
1052.64
InChiKey
NAZJRLKDOBAHOW-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

  • 作为反应物:
    描述:
    异氰酸叔丁酯 以 not given 为溶剂, 生成
    参考文献:
    名称:
    Synthesis of [(Me3SiNCH2CH2)3N]3- and [(C6F5NCH2CH2)3N]3- Complexes of Molybdenum and Tungsten That Contain CO, Isocyanides, or Ethylene
    摘要:
    Paramagnetic complexes of the type [N3N]MoL ([N3N](3-) = [(Me3SiNCH2CH2)(3)N](3-); L = CO, RNC, C2H4) have been prepared by displacing dinitrogen from [N3N]Mo(N-2). [N3N]Mo(CO) was reduced by magnesium powder in the presence of Me3SiCl to yield the diamagnetic oxycarbyne complex [N3N]Mo=COSiMe3, while oxidation of [N3N]Mo(CN-t-Bu) with [Cp2Fe]OTf yielded {[N3N]Mo(CN-t-Bu)}OTf. Thermolysis of [N3N]Mo(CN-t-Bu) resulted in loss of a t-Bu radical to yield [N3N]Mo(CN), which was structurally characterized, [N3NFML ([N3NF](3-) = [(C6F5NCH2CH2)(3)N](3-) M = Mo, W; L = CO, RNC) complexes have been prepared by one-electron reduction of [N3NF]M(OTf) in the presence of L. An X-ray study of [N3NF]W(CN-t-Bu) showed it to contain a bend isocyanide ligand. Anionic CO complexes were prepared by the two-electron reduction of [N3NF]M(OTf) in the presence of CO. An X-ray study of {[N3NF]W(CO)(2)}Na(ether)(3) revealed it to have a pseudo-octahedral structure in which sodium is bound to the CO trans tb the amine donor atom. Treatment of {[N3NF]M(CO)}(-) complexes with Me3SiCl gave oxycarbyne complexes [N3NF]M=COSiMe3. Reaction of [N3NF]WCO with V(Mes)(3)(THF) yielded [N3NF]W(CO)V(Mes)(3), the structure of which was determined in an X-ray study. Cationic [N3NF](3-) complexes could be prepared that contain up to 3 equiv of isocyanide. An X-ray study of {[N3NF]W(CN-t-Bu)(3)}BPh4 showed it to be a seven-coordinate species with one isocyanide located in the equatorial plane and the other two isocyanide ligands in the apical pocket. Reduction of [N3NF]W(OTf) under ethylene gave [N3NF]W(C2H4), which could be oxidized to yield diamagnetic {[N3NF]W(C2H4)}OTf.
    DOI:
    10.1021/om990748u
  • 作为产物:
    描述:
    N(CH2CH2NC6F5)3Mo(CNBu-t)四氢呋喃 为溶剂, 生成
    参考文献:
    名称:
    Synthesis of [(Me3SiNCH2CH2)3N]3- and [(C6F5NCH2CH2)3N]3- Complexes of Molybdenum and Tungsten That Contain CO, Isocyanides, or Ethylene
    摘要:
    Paramagnetic complexes of the type [N3N]MoL ([N3N](3-) = [(Me3SiNCH2CH2)(3)N](3-); L = CO, RNC, C2H4) have been prepared by displacing dinitrogen from [N3N]Mo(N-2). [N3N]Mo(CO) was reduced by magnesium powder in the presence of Me3SiCl to yield the diamagnetic oxycarbyne complex [N3N]Mo=COSiMe3, while oxidation of [N3N]Mo(CN-t-Bu) with [Cp2Fe]OTf yielded {[N3N]Mo(CN-t-Bu)}OTf. Thermolysis of [N3N]Mo(CN-t-Bu) resulted in loss of a t-Bu radical to yield [N3N]Mo(CN), which was structurally characterized, [N3NFML ([N3NF](3-) = [(C6F5NCH2CH2)(3)N](3-) M = Mo, W; L = CO, RNC) complexes have been prepared by one-electron reduction of [N3NF]M(OTf) in the presence of L. An X-ray study of [N3NF]W(CN-t-Bu) showed it to contain a bend isocyanide ligand. Anionic CO complexes were prepared by the two-electron reduction of [N3NF]M(OTf) in the presence of CO. An X-ray study of {[N3NF]W(CO)(2)}Na(ether)(3) revealed it to have a pseudo-octahedral structure in which sodium is bound to the CO trans tb the amine donor atom. Treatment of {[N3NF]M(CO)}(-) complexes with Me3SiCl gave oxycarbyne complexes [N3NF]M=COSiMe3. Reaction of [N3NF]WCO with V(Mes)(3)(THF) yielded [N3NF]W(CO)V(Mes)(3), the structure of which was determined in an X-ray study. Cationic [N3NF](3-) complexes could be prepared that contain up to 3 equiv of isocyanide. An X-ray study of {[N3NF]W(CN-t-Bu)(3)}BPh4 showed it to be a seven-coordinate species with one isocyanide located in the equatorial plane and the other two isocyanide ligands in the apical pocket. Reduction of [N3NF]W(OTf) under ethylene gave [N3NF]W(C2H4), which could be oxidized to yield diamagnetic {[N3NF]W(C2H4)}OTf.
    DOI:
    10.1021/om990748u
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