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[(C5H4Me)2Zr(C6F5)(ATMS)][B(C6F5)4] | 900791-33-5

中文名称
——
中文别名
——
英文名称
[(C5H4Me)2Zr(C6F5)(ATMS)][B(C6F5)4]
英文别名
[(C5H4Me)2Zr(C6F5)(allyltrimethylsilane)][B(C6F5)4]
[(C5H4Me)2Zr(C6F5)(ATMS)][B(C6F5)4]化学式
CAS
900791-33-5
化学式
C24BF20*C24H28F5SiZr
mdl
——
分子量
1209.83
InChiKey
BPULUCUCTSEOGH-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

反应信息

  • 作为产物:
    描述:
    [(C5H4Me)2Zr(C6F5)(C6D5Cl)][B(C6F5)4] 、 烯丙基三甲基硅烷 以 further solvent(s) 为溶剂, 生成 [(C5H4Me)2Zr(C6F5)(ATMS)][B(C6F5)4]
    参考文献:
    名称:
    Nonchelated Alkene and Alkyne Complexes of d0 Zirconocene Pentafluorophenyl Cations
    摘要:
    This paper describes the generation and properties of nonchelated d(0) zirconocene-aryl-alkene and alkyne adducts that are stabilized by the presence of beta-SiMe3 substituents on the substrates and the weak nucleophilicity of the -C6F5 ligand. The cationic complexes [(C5H4R)(2)Zr(C6F5)][B(C6F5)(4)] (4a: R) H, 4b: R) Me) were generated by methide abstraction from (C5H4R)(2)Zr(C6F5) Me by Ph3C+. NMR studies show that 4a,b contain an o-CF center dot center dot center dot Zr dative interaction and probably coordinate a PhCl molecule in PhCl solution. Addition of allyltrimethylsilane (ATMS) to 4a, b in C6D5Cl solution at low temperature produces an equilibrium mixture of (C5H4R)(2)Zr(C6F5)(H2CdCHCH2SiMe3)(+) (7a, b), 4a, b, and free ATMS. Similarly, addition of propargyltrimethylsilane (PTMS) to 4a produces an equilibrium mixture of Cp2Zr(C6F5)( HCtCCH(2)SiMe(3))(+) (8a), 4a, and free PTMS. The NMR data for 7a, b, and 8a are consistent with highly unsymmetrical substrate coordination and substantial polarization of the substrate multiple bond with significant positive charge buildup at C-int and negative charge buildup at C-term. PTMS binds to 4a more strongly than ATMS does. The ATMS adducts undergo nondissociative alkene face exchange ("alkene flipping"), i. e., exchange of the (C5H4R)(2)Zr(C6F5)(+) unit between the two alkene enantiofaces without decomplexation of the alkene, on the NMR time scale.
    DOI:
    10.1021/ja057524p
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