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fac-Y(CH2SiMe3)3(1,4,7-trithiacyclononane) | 1043413-30-4

中文名称
——
中文别名
——
英文名称
fac-Y(CH2SiMe3)3(1,4,7-trithiacyclononane)
英文别名
fac-Y(CH2SiMe3)3([9]aneS3)
fac-Y(CH2SiMe3)3(1,4,7-trithiacyclononane)化学式
CAS
1043413-30-4
化学式
C18H45S3Si3Y
mdl
——
分子量
530.916
InChiKey
ZFNJOMFRCCKIJE-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:
    bis(tetrahydrofuran)tris(trimethylsilylmethyl)yttrium(III) 、 1,4,7-三硫环壬烷氘代甲苯 为溶剂, 生成 fac-Y(CH2SiMe3)3(1,4,7-trithiacyclononane)
    参考文献:
    名称:
    Synthesis, DFT Studies, and Reactions of Scandium and Yttrium Dialkyl Cations Containing Neutral fac-N3 and fac-S3 Donor Ligands
    摘要:
    Reaction of Sc(CH2SiMe3)(3)(THF)(2) with 1,4,7-trithiacyclononane gave Sc([9]aneS(3))(CH2SiMe3)(3), the first organometallic group 3 complex of [9]aneS(3) ([9]aneS(3) = 1,4,7-trithiacyclononane). The corresponding reaction for yttrium gave equilibrium mixtures of Y([9]aneS(3))(CH2SiMe3)(3) and starting materials. Density functional theory (DFT) was used to compare the energies of formation and metal-ligand interaction energies for M([9]aneS(3))R-3 with those for the previously reported fac-N-3 donor complexes M(fac-N-3)R-3 (R = Me or CH2SiMe3; fac-N-3 = 1,4,7-trimethyltriazacyclononane (Me-3[9]aneN(3)) or HC(Me(2)pz)(3)). Reaction of M(CH2SiMe3)(3)(THF)(2) with [NHMe2Ph][BAr4F] (Ar-F = C6F5) in the presence of a facecapping ligand L (L = HC(Me(2)pz)(3), Me-3[9]aneN(3), or [9]aneS(3)) gave the cationic complexes [M(L)(CH2SiMe3)2(THF)](+), which has been structurally characterized for M = Sc and L = [9]aneS3. The corresponding base-free cations [M(L)(CH2SiMe3)(2)](+) were studied by Si-29 NMR spectroscopy and/or DFT and found to possess beta-Si-C agostic alkyl groups in most instances. The isolated cations [Sc(fac-N-3)(CH2SiMe3)(2)(THF)](+) underwent THF substitution reactions with OPPh3 or pyridine, Sc-alkyl migratory insertion with carbodiimides, and C-H bond metathesis with PhCCH. The olefin polymerization capabilities of a series of complexes M(L)R3 have been determined. The scandium complexes were found to be very productive for ethylene polymerization for L (L = HC(Me(2)pz)(3), Me-3[9]aneN(3), or [9]aneS(3) and R = CH2SiMe3 when activated with 1 equiv of [CPh3][BAr4F]. When activated with 2 equiv of [CPh3][BAr4F], the compounds were also very active for the polymerization of 1-hexene.
    DOI:
    10.1021/om800279d
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