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Dithiophosphoric acid O,O'-dinaphthalen-1-yl ester | 50566-50-2

中文名称
——
中文别名
——
英文名称
Dithiophosphoric acid O,O'-dinaphthalen-1-yl ester
英文别名
——
Dithiophosphoric acid O,O'-dinaphthalen-1-yl ester化学式
CAS
50566-50-2
化学式
C20H15O2PS2
mdl
——
分子量
382.444
InChiKey
GCDJYVDLUBSDOT-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):
    6.61
  • 重原子数:
    25.0
  • 可旋转键数:
    4.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    18.46
  • 氢给体数:
    1.0
  • 氢受体数:
    3.0

反应信息

  • 作为反应物:
    描述:
    Dithiophosphoric acid O,O'-dinaphthalen-1-yl estersodium 作用下, 以 甲苯 为溶剂, 反应 3.0h, 以88.55%的产率得到
    参考文献:
    名称:
    Synthesis and Characterization of O,O'-Bis(α-Naphthyl, β-Naphthyl, and 2, 3, 5-Trimethylphenyl)Dithiophosphate Ligands
    摘要:
    O,O'-Bis(alpha-Naphthyl, beta-Naphthyl and 2,3,5-trimethylphenyl) dithiophosphate ligands have been isolated as triethylammonium salts, (alpha-C10H7O-, beta-C10H7O, and (CH3)(3)C6H2O)(2)PS2HNEt3, by the reaction of alpha-C10H7OH, beta-C10H7OH, or (CH3)(3)C6H2OH with P2S5 in presence of Et3N, in 4:1:2 molar ratio in chloroform under anhydrous conditions. Acidic form of these ligands, (alpha-C10H7O-, beta-C10H7O-, or (CH3)(3)C6H2O)(2)PS2H, have been obtained by the direct reaction of alpha-C10H7OH, beta-C10H7OH-, or (CH3)(3)C6H2OH with P2S5 in 4:1 molar ratio in presence of microwaves under solvent-free conditions. Both forms of the ligands have been converted into corresponding sodium salts, (alpha-C10H7O-, beta-C10H7O-, or (CH3)(3)C6H2O)(2)PS2Na. These compounds have been characterized by elemental analyses (C, H, N, and S) and mass, IR, and NMR (H-1, C-13 and P-31) spectroscopic studies.Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file.
    DOI:
    10.1080/10426507.2012.680081
  • 作为产物:
    描述:
    萘酚tetraphosphorus decasulfide 作用下, 反应 0.07h, 以99.3%的产率得到Dithiophosphoric acid O,O'-dinaphthalen-1-yl ester
    参考文献:
    名称:
    Synthesis and Characterization of O,O'-Bis(α-Naphthyl, β-Naphthyl, and 2, 3, 5-Trimethylphenyl)Dithiophosphate Ligands
    摘要:
    O,O'-Bis(alpha-Naphthyl, beta-Naphthyl and 2,3,5-trimethylphenyl) dithiophosphate ligands have been isolated as triethylammonium salts, (alpha-C10H7O-, beta-C10H7O, and (CH3)(3)C6H2O)(2)PS2HNEt3, by the reaction of alpha-C10H7OH, beta-C10H7OH, or (CH3)(3)C6H2OH with P2S5 in presence of Et3N, in 4:1:2 molar ratio in chloroform under anhydrous conditions. Acidic form of these ligands, (alpha-C10H7O-, beta-C10H7O-, or (CH3)(3)C6H2O)(2)PS2H, have been obtained by the direct reaction of alpha-C10H7OH, beta-C10H7OH-, or (CH3)(3)C6H2OH with P2S5 in 4:1 molar ratio in presence of microwaves under solvent-free conditions. Both forms of the ligands have been converted into corresponding sodium salts, (alpha-C10H7O-, beta-C10H7O-, or (CH3)(3)C6H2O)(2)PS2Na. These compounds have been characterized by elemental analyses (C, H, N, and S) and mass, IR, and NMR (H-1, C-13 and P-31) spectroscopic studies.Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file.
    DOI:
    10.1080/10426507.2012.680081
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文献信息

  • Transition metal complexes of organothiophosphorous ligands V.Some aryl esters and amides of dithiophosphoric acid and their nickel(II) and cobalt(II and III)complexes
    作者:R. Micu-Semeniuc、L. Dumitrescu-Silaghi、I. Haiduc
    DOI:10.1016/s0020-1693(00)89489-x
    日期:1979.1
    decasulfide reacted with phenoxyethanol, α and β-naphthol, ortho-toluidine, ortho-aminophenol and ortho-phenylenediamine to give aryl esters or amides of dithiophosphoric acids. These were used as ligands in the synthesis of some nickel(II) and cobalt(II and III) complexes. With para-toluidine only the amide (p-CH3C6H4NH)3PS was isolated.
    摘要四化碳与苯氧基乙醇,α和β-萘酚邻甲苯胺,邻氨基苯酚邻苯二胺反应,生成二硫代磷酸的芳基酯或酰胺。这些在某些(II)和(II和III)配合物的合成中用作配体。用对甲苯胺仅分离出酰胺(p-CH 3 C 6 H 4 NH)3 PS。
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