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2,7-bis(ferrocenylethynyl)-9,9-dihexylfluorene | 841243-95-6

中文名称
——
中文别名
——
英文名称
2,7-bis(ferrocenylethynyl)-9,9-dihexylfluorene
英文别名
——
2,7-bis(ferrocenylethynyl)-9,9-dihexylfluorene化学式
CAS
841243-95-6
化学式
C49H50Fe2
mdl
——
分子量
750.63
InChiKey
QXRHKXKPXUPBSP-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):
    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

  • 作为产物:
    描述:
    二茂铁乙炔9,9-二己基-2,7-二溴代芴 在 Pd(O2CCH3)2 、 PPh3 、 CuI 作用下, 以 further solvent(s) 为溶剂, 以80%的产率得到2,7-bis(ferrocenylethynyl)-9,9-dihexylfluorene
    参考文献:
    名称:
    Carbon-rich organometallics: synthesis and characterization of new ferrocenyl end-capped bis(butadiynyl) fluorene derivatives
    摘要:
    A new series of ferrocenyl end-capped bis(butadiynyl) fluorene complexes [(eta(5)-C5H5)Fe(eta(5)-C5H4)CdropCCdropCRCdropCCdropC-(eta(5)-C5H4)Fe(eta(5)-C5H5)] (R = fluoren-9-one-2,7-diyl, 1; 9,9-dihexylfluorene-2,7-diyl, 2; 9-ferrocenylmethylenefluorene-2,7-diyl, 3; 9-ferrocenylphenylmethylenefluorene-2,7-diyl, 4) have been synthesized in moderate yields by the oxidative coupling reactions of ethynylferrocene with half equivalents of the appropriate diethynylfluorene derivatives. All the new complexes have been characterized by FTIR. NMR and UV-vis spectroscopies and fast atom bombardment mass spectrometry. The molecular structures of selected molecules have been determined by X-ray crystallographic techniques. The electronic absorption and redox properties of these carbon-rich molecules were investigated and the data were compared with those for the corresponding 2,7-bis(ferrocenylethynyl)fluorene counterparts. Cyclic voltammetry indicates that the half-wave potential of the terminal ferrocenyl moieties becomes more anodic when the number of ethynyl units increases and when the 9-substituent of the central fluorene ring changes from an electron-donating group to an electron-deficient group. (C) 2004 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2004.09.008
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