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3,4,6,7-tetrathio-9-hydroxyphenalen-1-one | 1425265-61-7

中文名称
——
中文别名
——
英文名称
3,4,6,7-tetrathio-9-hydroxyphenalen-1-one
英文别名
8-Hydroxy-2,3,11,12-tetrathiapentacyclo[11.3.1.04,16.07,15.010,14]heptadeca-1(16),4,7(15),8,10(14),13(17)-hexaen-6-one;8-hydroxy-2,3,11,12-tetrathiapentacyclo[11.3.1.04,16.07,15.010,14]heptadeca-1(16),4,7(15),8,10(14),13(17)-hexaen-6-one
3,4,6,7-tetrathio-9-hydroxyphenalen-1-one化学式
CAS
1425265-61-7
化学式
C13H4O2S4
mdl
——
分子量
320.438
InChiKey
LCJSJNLTGFXLEC-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):
    3.5
  • 重原子数:
    19
  • 可旋转键数:
    0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    139
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    三氟甲磺酸3,4,6,7-tetrathio-9-hydroxyphenalen-1-one劳森试剂 作用下, 以 氯苯 为溶剂, 反应 36.0h, 以8%的产率得到1,2,4,5,7,8-hexathiophenalenylium triflate
    参考文献:
    名称:
    Hexathiophenalenylium Cations: Syntheses, Structures, and Redox Chemistry
    摘要:
    Preparations of two hexathiophenalenylium compounds as stable salts from the reaction of 3,4,6,7-tetrathio-9-hydroxyphenalenone with Lawesson's reagent have been reported. The presence of three disulfide linkages on the periphery of the core phenalenyl unit is confirmed by X-ray crystallographic characterizations. Electrochemical cell potentials are lower than those of related dithio- and tetrathio-bridged phenalenyl radicals, and the hexathiophenalenyl radical shows a strong electron paramagnetic resonance (EPR) signal in the solid state.
    DOI:
    10.1021/ol400452f
  • 作为产物:
    描述:
    1,3,6,8-tetramethoxynaphthalene 在 盐酸吡啶盐酸盐三乙胺potassium thioacetate 作用下, 以 二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 95.0h, 生成 3,4,6,7-tetrathio-9-hydroxyphenalen-1-one
    参考文献:
    名称:
    Hexathiophenalenylium Cations: Syntheses, Structures, and Redox Chemistry
    摘要:
    Preparations of two hexathiophenalenylium compounds as stable salts from the reaction of 3,4,6,7-tetrathio-9-hydroxyphenalenone with Lawesson's reagent have been reported. The presence of three disulfide linkages on the periphery of the core phenalenyl unit is confirmed by X-ray crystallographic characterizations. Electrochemical cell potentials are lower than those of related dithio- and tetrathio-bridged phenalenyl radicals, and the hexathiophenalenyl radical shows a strong electron paramagnetic resonance (EPR) signal in the solid state.
    DOI:
    10.1021/ol400452f
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文献信息

  • Synthesis of Tetrachalcogenide-Substituted Phenalenyl Derivatives: Preparation and Solid-State Characterization of Bis(3,4,6,7-tetrathioalkyl-phenalenyl)boron Radicals
    作者:Pradip Bag、Sushanta K. Pal、Mikhail E. Itkis、Arindam Sarkar、Fook S. Tham、Bruno Donnadieu、Robert C. Haddon
    DOI:10.1021/ja405814f
    日期:2013.9.4
    We report the synthesis and properties of a series of spiro-bis(3,4,6,7-tetrachalcogenide-substituted-phenalenyl)boron salts and two of the corresponding tetrathioalkyl-substituted spiro-bis(phenalenyl)boron radicals [tetrathiomethyl (10) and tetrathioethyl (11)] in which all of the active positions of the phenalenyl (PLY) nucleus are functionalized. In the solid state, radicals 10 and 11 exist as a weak pi-dimers due to the steric congestion of the thioalkyl groups in the superimposed PLY units. As a result, the spins are localized in the isolated (nonsuperimposed) PLY rings, and the structure, magnetic susceptibility measurements, and band structure calculations confirm that these PLY units are unable to undergo strong intermolecular interaction as a result of the orientation of the thioalkyl groups.
  • Hexathiophenalenylium Cations: Syntheses, Structures, and Redox Chemistry
    作者:Pradip Bag、Fook S. Tham、Bruno Donnadieu、Robert C. Haddon
    DOI:10.1021/ol400452f
    日期:2013.3.15
    Preparations of two hexathiophenalenylium compounds as stable salts from the reaction of 3,4,6,7-tetrathio-9-hydroxyphenalenone with Lawesson's reagent have been reported. The presence of three disulfide linkages on the periphery of the core phenalenyl unit is confirmed by X-ray crystallographic characterizations. Electrochemical cell potentials are lower than those of related dithio- and tetrathio-bridged phenalenyl radicals, and the hexathiophenalenyl radical shows a strong electron paramagnetic resonance (EPR) signal in the solid state.
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