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[Hf(η5-C5H4SiMe2(CH2CH=CH2))Cl3*DME] | 867043-72-9

中文名称
——
中文别名
——
英文名称
[Hf(η5-C5H4SiMe2(CH2CH=CH2))Cl3*DME]
英文别名
——
[Hf(η5-C5H4SiMe2(CH2CH=CH2))Cl3*DME]化学式
CAS
867043-72-9
化学式
C4H10O2*C10H15Cl3HfSi
mdl
——
分子量
538.286
InChiKey
QRFPJVOKIXCHJT-UHFFFAOYSA-K
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:
    [Hf(η5-C5H4SiMe2(CH2CH=CH2))Cl3*DME]苄基氯化镁四氢呋喃乙醚 为溶剂, 以33%的产率得到[Hf(η5-C5H4SiMe2(CH2CH=CH2))(CH2Ph)3]
    参考文献:
    名称:
    Allyldimethylsilylcyclopentadienyl Hafnium Complexes:  Formation and Trapping of Hafnocenium Cations
    摘要:
    The mixed silyl-stannyl-cyclopentadiene C5H4[SiMe2(CH2CH=CH2)] [Sn(nBu)(3)] was synthesized by reaction of the lithium salt Li[C5H4{SiMe2(CH2CH=CH2)}] with the corresponding chlorotrialkyltin and then reacted with HfCl4 to prepare the monocyclopentadienyl complex [Hf{eta(5)-C5H4SiMe2(CH2CH=CH2)}Cl-3 center dot DME] (DME = dimethoxyethane). Reaction of this compound with Na(C5H5) or Li(C5H5) afforded low yields of the dichloro hafhocene [Hf(eta(5)-C5H5){eta(5)-C5H4SiMe2(CH2CH=CH2)}Cl-2], which was also isolated more efficiently by transmetalation of the lithium salt Li[C5H4{SiMe2(CH2CH=CH2)}] with [Hf(eta(5)-C5H5)Cl-3 center dot DME]. Alkylation of the mono- and dicyclopentadienyl complexes with MgCl(CH2Ph) or LiMe gave the tribenzyl monocyclopentadienyl [Hf(eta(5)-C5H4SiMe2(CH2CH=CH2)}(CH2Ph)(3)] or the dialkyl hafhocene derivatives [Hf(eta(5)-C5H5){eta(5)-C5H4SiMe2(CH2CH=CH2)R-2] (R = Me, CH2Ph). The reaction of the dibenzyl hafhocene with the Lewis acid B(C6F5)(3) was monitored by NMR spectroscopy at variable temperature. Formation of the hafhocenium cationic species [Hf(eta(5) -C5H5){eta(5)-C5H4SiMe2(CH2-eta(2)-CH=CH2)}(CH2Ph)(+) was initially observed, which then slowly transformed into the metallacyclic alkyl [Hf(eta(5)-C5H5){eta(5)-C5H4SiMe2CH2CH(CH2Ph)eta(1)-CH2}](+) cation, resulting from the benzyl migratory insertion of the allylic alkene moiety. Reaction of these intermediate cationic species with KOtBu gave the neutral dicyclopentadienyl hafhocene compounds [Hf(eta(5)-C5H5){eta(5)-C5H4SiMe2(CH2CH=CH2)}(CH2Ph)(OtBu)] and [Hf(eta(5)-C5H5){eta(5)-C5H4SiMe2[CH2CH(CH2Ph)-eta(1)-CH2]}(OtBu)], which were characterized by elemental analyses and NMR spectroscopy.
    DOI:
    10.1021/om050437l
  • 作为产物:
    描述:
    乙二醇二甲醚二甲基硫dimethyl-prop-2-enyl-(1-tributylstannylcyclopenta-2,4-dien-1-yl)silane氯化铪二氯甲烷 为溶剂, 以59%的产率得到[Hf(η5-C5H4SiMe2(CH2CH=CH2))Cl3*DME]
    参考文献:
    名称:
    Allyldimethylsilylcyclopentadienyl Hafnium Complexes:  Formation and Trapping of Hafnocenium Cations
    摘要:
    The mixed silyl-stannyl-cyclopentadiene C5H4[SiMe2(CH2CH=CH2)] [Sn(nBu)(3)] was synthesized by reaction of the lithium salt Li[C5H4{SiMe2(CH2CH=CH2)}] with the corresponding chlorotrialkyltin and then reacted with HfCl4 to prepare the monocyclopentadienyl complex [Hf{eta(5)-C5H4SiMe2(CH2CH=CH2)}Cl-3 center dot DME] (DME = dimethoxyethane). Reaction of this compound with Na(C5H5) or Li(C5H5) afforded low yields of the dichloro hafhocene [Hf(eta(5)-C5H5){eta(5)-C5H4SiMe2(CH2CH=CH2)}Cl-2], which was also isolated more efficiently by transmetalation of the lithium salt Li[C5H4{SiMe2(CH2CH=CH2)}] with [Hf(eta(5)-C5H5)Cl-3 center dot DME]. Alkylation of the mono- and dicyclopentadienyl complexes with MgCl(CH2Ph) or LiMe gave the tribenzyl monocyclopentadienyl [Hf(eta(5)-C5H4SiMe2(CH2CH=CH2)}(CH2Ph)(3)] or the dialkyl hafhocene derivatives [Hf(eta(5)-C5H5){eta(5)-C5H4SiMe2(CH2CH=CH2)R-2] (R = Me, CH2Ph). The reaction of the dibenzyl hafhocene with the Lewis acid B(C6F5)(3) was monitored by NMR spectroscopy at variable temperature. Formation of the hafhocenium cationic species [Hf(eta(5) -C5H5){eta(5)-C5H4SiMe2(CH2-eta(2)-CH=CH2)}(CH2Ph)(+) was initially observed, which then slowly transformed into the metallacyclic alkyl [Hf(eta(5)-C5H5){eta(5)-C5H4SiMe2CH2CH(CH2Ph)eta(1)-CH2}](+) cation, resulting from the benzyl migratory insertion of the allylic alkene moiety. Reaction of these intermediate cationic species with KOtBu gave the neutral dicyclopentadienyl hafhocene compounds [Hf(eta(5)-C5H5){eta(5)-C5H4SiMe2(CH2CH=CH2)}(CH2Ph)(OtBu)] and [Hf(eta(5)-C5H5){eta(5)-C5H4SiMe2[CH2CH(CH2Ph)-eta(1)-CH2]}(OtBu)], which were characterized by elemental analyses and NMR spectroscopy.
    DOI:
    10.1021/om050437l
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