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4,4'-(naphthalene-1,8-diyl)dibenzimidamide nonanedioate | 1610972-98-9

中文名称
——
中文别名
——
英文名称
4,4'-(naphthalene-1,8-diyl)dibenzimidamide nonanedioate
英文别名
——
4,4'-(naphthalene-1,8-diyl)dibenzimidamide nonanedioate化学式
CAS
1610972-98-9
化学式
C9H16O4*C24H20N4
mdl
——
分子量
552.673
InChiKey
GIYHEKOMYATKQE-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):
    6.63
  • 重原子数:
    41.0
  • 可旋转键数:
    12.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    174.34
  • 氢给体数:
    6.0
  • 氢受体数:
    4.0

反应信息

  • 作为产物:
    描述:
    1,8-bis(4-amidinophenyl)naphthalene dihydrochloride 在 、 sodium hydroxide 作用下, 以 二甲基亚砜 为溶剂, 反应 0.08h, 生成 4,4'-(naphthalene-1,8-diyl)dibenzimidamide nonanedioate
    参考文献:
    名称:
    Fluorescent detection of amidinium-carboxylate and amidinium formation using a 1,8-diphenylnaphthalene-based diamidine: dicarboxylic acid recognition with high fluorescence efficiency
    摘要:
    A 1,8-diphenyinaphthalene-based diamidine (1) 'turn-on' fluorescent probe for the detection of dicarboxylic acids has been designed and synthesized. The fluorescence spectra of the diamidine 1 with carboxylic acids that showed two different fluorescence bands, which corresponded to the amidinium-carboxylate (lambda(em)=410-430 nm) and amidinium (lambda(em)=440-470 nm as a broad band, which consisted from two peaks) formation, were confirmed by DOSY NMR and TD-DFT calculations. The complexation of diamidine 1 with dicarboxylic acids, which have sufficient distances between the two carboxylic groups for binding to the diamidine 1 (dicarboxylic acids 3, 4, and alpha,omega-dicarboxylic acids 6 (C-6-C-20)), showed the formation of 1:1 complexes (i.e., amidinium-carboxylate formation). On the other hand, for the complexation with monocarboxylic acids and dicarboxylic acids having insufficient distances between the two carboxylic groups (benzoic acid 5, acetic acid 7, and alpha,omega-dicarboxylic acids 6 (C-3-C-5)), formation of the amidinium (1.2H(+)) was observed. Relatively similar binding constants (10(-5)) for the complexation of the diamidine 1 with dicarboxylic acids 6, which depend on their chain length (strain), were observed due to the flexibility of the 1,8-diphenylnaphthalene unit. Additionally, for the complexation of the diamidine 1 with dicarboxylic acids, higher fluorescence quantum yields (Phi(fl): up to 80%) were observed when compared to the binding of the diamidine 2 (Phi(fl): up to 35%). (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2014.03.036
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