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N,N,N-Tributyl-N-(2-methylnaphthalene)ammonium bromide | 25316-74-9

中文名称
——
中文别名
——
英文名称
N,N,N-Tributyl-N-(2-methylnaphthalene)ammonium bromide
英文别名
N-(2-Naphthyl methyl)-N,N,N-tributyl ammonium bromide;tributyl(naphthalen-2-ylmethyl)azanium;bromide
N,N,N-Tributyl-N-(2-methylnaphthalene)ammonium bromide化学式
CAS
25316-74-9
化学式
Br*C23H36N
mdl
——
分子量
406.45
InChiKey
BVJPRZIBQNQARS-UHFFFAOYSA-M
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):
    3.56
  • 重原子数:
    25
  • 可旋转键数:
    11
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    参考文献:
    名称:
    Photoinduced Electron-Transfer Reactions:  Highly Efficient Cleavage of C−N Bonds and Photogeneration of Tertiary Amines
    摘要:
    The photocleavage of tertiary amine from tetraphenylborates complexed, via ammonium ions, to various chromophore electron accepters has been studied by laser-flash photolysis. Electron transfer from the berate anions to acceptor excited states is determined to be the primary photochemical step leading to homolytic C-N bond scission and concomitant formation of the corresponding tertiary amine. This pathway was established by direct observation of p-benzoylbenzyl (7a), p-acetylbenzyl (7b), beta-naphthylmethyl (7c), and 7-methoxycoumarin-4-methyl (7d) after laser-flash photolysis from N-(4-benzoyl)benzyl-N,N,N-tributylammonium tetraphenylborate (1a), N-(4-acetyl)benzyl-N,N,N-trimethylammonium tetraphenylborate (1b) N,N,N-tributyl-N-(2-methylnaphthalene)ammonium tetraphenylborate (1c), and N,N,N-tributyl-N-(4-methyl-7-methoxycoumarin)ammonium tetraphenylborate (1d), respectively. The presence of radicals (7a-7d) was also suggested by the reaction products. Comparison of the rate constants for quenching of the tripler states from excited (1a, 1b) and singlet states from (1c, 1d) reveals the efficiency of C-N bond cleavage. Quenching constants in the range of 10(9)-10(12) M-1 s(-1) were observed. Differences are accounted for in terms of variations in the electron-accepting excited states and structural characteristics of the chromophore accepters.
    DOI:
    10.1021/jp972855c
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