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(η(5)-C5Me4Et)ZrF3 | 173725-09-2

中文名称
——
中文别名
——
英文名称
(η(5)-C5Me4Et)ZrF3
英文别名
——
(η(5)-C5Me4Et)ZrF3化学式
CAS
173725-09-2
化学式
C11H17F3Zr
mdl
——
分子量
297.475
InChiKey
RSAIOARCGCZDPN-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

反应信息

  • 作为反应物:
    描述:
    (η(5)-C5Me4Et)ZrF3三甲基铝正己烷 为溶剂, 以70%的产率得到[((η(5)-C5Me4Et)Zr)3Al6Me8(μ3-CH2)2(μ4-CH)4(μ3-CH)]
    参考文献:
    名称:
    Reactions of (η5-C5Me5)ZrF3, (η5-C5Me4Et)ZrF3, (η5-C5Me5)2ZrF2, (η5-C5Me5)HfF3, and (η5-C5Me5)TaF4 with AlMe3. Structure of the First Hafnium−Aluminum−Carbon Cluster
    摘要:
    The reaction of Cp*ZrF3 (1) (Cp* = eta(5)-C(5)Me(5)) and AlMe(3) resulted in the formation of cis-{[Cp*ZrMe(mu(2)-F)][(mu(2)-F)(2)AlMe(2)]}(2) (6) and [(Cp*Zr)(3)Al(6)Me(8)(mu(3)-CH2)(2)(mu(4)-CH)(4)(mu(3)-CH)] (7), respectively. Analogously, (eta(5)-C(5)Me(4)Et)ZrF3 (3) reacts with AlMe(3) in a molar ratio of 1:5 with I methane elimination to give the Zr3Al6C7 cluster of composition {[(eta(5)-C(5)Me(4)Et)Zr](3)Al(6)Me(8)(mu(3)-CH2)(2)(mu(4)-CH)(4)(mu(3)-CH)} (8), which has been characterized by elemental analysis and H-1 NMR and mass spectrometry. Reaction of 2 equiv of AlMe(3) with CP*2ZrF2 (2) leads quantitatively to Cp*(2)ZrMe(2) (12). Reaction of Cp*HfF3 (4) with AlMe(3) in an equimolar ratio gives {[Cp*HfMe (mu(2)-F)][(mu(2)-F)(2)AlMe(2)]}(2) (9) stereospecifically as its cis isomer in high yield. 9 crystallizes in the space group P2(1)/c with four molecules in the elemental cell (Z = 16). From the reaction of 1 equiv of Cp*HfF3 (4) with 3 equiv of AlMe(3), Cp*HfMe(3) (10) can be obtained in a yield of 85%. As a byproduct of this reaction the Hf3Al6C7 cluster [(Cp*Hf)(3)Al(6)Me(8)(mu(3)-CH2)(2)(mu(4)-CH)(4)(mu(3)-CH)] (11) can be isolated in a yield of 5%. The characterization of 11 by single-crystal X-ray diffraction and H-1, C-13 NMR and mass spectroscopic data will be discussed. Cp*TaF4 (5) reacts with a 5-fold excess of AlMe(3), leading quantitatively to Cp*TaMe(4) (13) without further decomposition via C-H activation processes.
    DOI:
    10.1021/om950590n
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