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(η(5)-exo-6-(dichloromethyl)-1,3,5-trimethylcyclohexadienyl)(η(6)-mesitylene)iron(II) hexafluorophosphate | 137465-44-2

中文名称
——
中文别名
——
英文名称
(η(5)-exo-6-(dichloromethyl)-1,3,5-trimethylcyclohexadienyl)(η(6)-mesitylene)iron(II) hexafluorophosphate
英文别名
——
(η(5)-exo-6-(dichloromethyl)-1,3,5-trimethylcyclohexadienyl)(η(6)-mesitylene)iron(II) hexafluorophosphate化学式
CAS
137465-44-2
化学式
C19H25Cl2Fe*F6P
mdl
——
分子量
525.125
InChiKey
WCKRXZSAPWQNGW-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:
    [Fe(η(6)-1,3,5-trimethylbenzene)2](PF6)2 在 {N(CH2CH2O)3Al2(CH3)3}2 、 CH2Cl2 作用下, 以 二氯甲烷 为溶剂, 以45%的产率得到(η(5)-exo-6-(dichloromethyl)-1,3,5-trimethylcyclohexadienyl)(η(6)-mesitylene)iron(II) hexafluorophosphate
    参考文献:
    名称:
    烷基铝试剂与有机过渡金属芳烃配合物的相互作用:将烷基化物,卤代烷基化物和二氯甲基净添加到[(arene)2Fe] 2+阳离子中
    摘要:
    AlEt3 reacts with the hexafluorophosphate salts of Ar2Fe2+ cations (Ar = arene = benzene (1a), p-xylene (1b), mesitylene (1c), pentamethylbenzene (1d), hexamethylbenzene (1e)) in dichloromethane or 1,2-dichloroethane to afford ChArFe+ (Ch = cyclohexadienyl) cations. The major products, the hexafluorophosphate salts of 2a-e, result from net Et- addition to a single arene ring. The corresponding reactions with AlMe3 in CH2X2 (X = Cl, Br) are more complex and afford characterizable products for 1c,e only. The unexpected major products of these reactions are the hexafluorophosphate salts of the [(6-CH2X-Ch)ArFe]+ monocations 3c,e (X = Cl) and 4c,e (X = Br), derived from net addition of CH2X, rather than the expected methide addition products, 5a-e. 1c reacts with [N(CH2CH2O)3Al2Me3]2 (6), a compound that contains an octahedral aluminum methyl moiety, in dichloromethane to produce yet another ChArFe+ species, (eta(5)-exo-6-(dichloromethyl)-1,3,5-trimethylcyclohexadienyl)(eta(6)-mesitylene)iron(II) hexafluorophosphonate (7c[PF6]), which is the result of net addition of CHCl2-. The methide addition monocationic product 5c[PF6] can be prepared in low yield from AlMe3 or 6 and 1c if benzene and 1,2-dichloroethane, respectively, are utilized as solvent. The relevance of these reactions is discussed in the general context of transition-metal activation of Ar molecules. In addition to spectroscopic characterization, several compounds were characterized by X-ray crystallography. Full crystallographic details of the CH2Cl-Ch and CHCl2-Ch cations 3c and 7c, respectively, are presented and discussed in the context of related ChFe compounds: 3c[PF6], orthorhombic, Pcab, with a = 15.2496 (9) angstrom, b = 15.5537 (10) angstrom, c = 17.5146 (16) angstrom, Z = 8, R = 0.059, R(w) = 0.058 for 2506 independent, observed (I > 2.5-sigma(I)), and absorption-corrected reflections; 7c[PF6].(CH3)2CO, monoclinic, P2(1)/c, with a = 18.762 (3) angstrom, b = 8.758 (2) angstrom, c = 17.104 (3) angstrom, beta = 113.40 (2)-degrees, Z = 4, R = 0.049, R(w) = 0.055 for 2051 independent, observed (I > 2.5-sigma(I)), and absorption-corrected reflections.
    DOI:
    10.1021/om00037a057
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