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3-fluorophenyldifluoroborane | 32038-78-1

中文名称
——
中文别名
——
英文名称
3-fluorophenyldifluoroborane
英文别名
m-Fluorphenylbordifluorid;m-FC6H4BF2;Difluoro-(3-fluorophenyl)borane;difluoro-(3-fluorophenyl)borane
3-fluorophenyldifluoroborane化学式
CAS
32038-78-1
化学式
C6H4BF3
mdl
——
分子量
143.904
InChiKey
IGPGUJDHMUBJCJ-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):
    1.46
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    五氟(二氟碘)苯3-fluorophenyldifluoroborane二氯甲烷 为溶剂, 以73%的产率得到(m-fluorophenyl)(pentafluorophenyl)iodonium tetrafluoroborate
    参考文献:
    名称:
    摘要:
    Aryl(pentafluorophenyl)iodoniumtetrafluoroborates [Ar'Ar "I][BF4] (Ar' = C6F5, Ar " = C6H5, o-C6H4F, m-C6H4F p-C6H4F, 2,6-C6H3F2, 3,5-C6H3F2, 2,4,6-C6H2F3, 3,4,5-C6H2F3, C6F5) are prepared in good yields and high purity by the reaction of C6F6IF2 with Ar " BF2 in CH2Cl2. This convenient method can be applied generally to many iodonium compounds. Thermal and spectroscopic properties (H-1, C-13, F-19 NMR, IR, Raman) are reported and discussed. The solid state structures of six iodonium compounds show significant cation-anion interactions which result in two different arrangements: a dimer with a 8-membered ring or polymers with infinite zigzag chains. Ab initio calculations on prototypes of aryliodonium cations show relations between the kind of the aryl group (C6H5 vs. C6F5) and structural parameters as well as charges. By means of F-19 NMR the sigma (1)- and sigma (R)-constants of the [C6F5I](+)-substituent are determined.
    DOI:
    10.1002/1521-3749(200011)626:11<2419::aid-zaac2419>3.0.co;2-k
  • 作为产物:
    描述:
    间溴氟苯二氟化氢钾三氟化硼magnesium 作用下, 以 甲醇乙醚二氯甲烷 为溶剂, 反应 5.0h, 生成 3-fluorophenyldifluoroborane 、 alkaline earth salt of/the/ methylsulfuric acid
    参考文献:
    名称:
    (Fluoroorgano)fluoroboranes and -fluoroborates I: synthesis and spectroscopic characterization of potassium fluoroaryltrifluoroborates and fluoroaryldifluoroboranes
    摘要:
    A convenient preparation of K[ArBF3] (Ar= 2-C6H4F, 3-C6H4F, 4-C6H4F, 2,6-C6H3F2, 3,5-C6H3F2, 2,4,6-C6H2F3, 3,4,5-C6H2F3, 2,3,4,5-C6HF4 and C6F5) is offered and the IR and multinuclear NMR spectra of these salts are reported. Treatment of the trifluoroborate salts with BF3 in chlorocarbon solvents provides an easy synthetic route to the corresponding aryldifluoroboranes ArBF2. The multinuclear NMR spectra of ArBF2 are presented. The electron substituent effect of the [-BF3](-)-group shows this substituent as one of the strongest sigma-electron donors, while its pi-electron influence is negligible (sigma(I) = - 0.32, sigma(R) = - 0.07). (C) 2000 Elsevier Science S.A. All rights reserved.
    DOI:
    10.1016/s0022-328x(99)00690-7
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文献信息

  • Synthesis of Fluorine-Containing Aryl(halo)boranes from Potassium Aryl(fluoro)borates
    作者:V. V. Bardin、S. A. Prikhod’ko、M. M. Shmakov、A. Yu. Shabalin、N. Yu. Adonin
    DOI:10.1134/s1070363220010089
    日期:2020.1
    Fluorine-containing aryldihalogenoboranes have been obtained by the reaction of boron and aluminum chlorides and bromides with potassium aryltrifluoroborates K[ArBF3] under mild conditions. In a similar way, bis(pentafluorophenyl)halogenoboranes have been synthesized by the reaction with K[(C6F5)2BF2]. The reaction of K[C6F5BF3] with AlBr3 affords a mixture of C6F5BF2 and C6F5BCl2 due to fast conversion
    通过在温和的条件下使化铝与化物与芳基三硼酸K [ArBF 3 ]反应,可获得含的芳基二卤化硼烷。以类似的方式,通过与K [(C 6 F 5)2 BF 2 ]的反应合成了双(五氟苯基)卤代硼烷。K [C 6 F 5 BF 3 ]与AlBr 3的反应产生C 6 F 5 BF 2和C 6 F 5 BCl 2的混合物,这是由于AlBr 3快速转化为AlBrCl2。计算了BCl 2和BBr 2组的感应和共振参数。
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