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cis,cis,cis-2,5,8-tribenzyltrindane-2,5,8-tricarboxylic acid | 410074-26-9

中文名称
——
中文别名
——
英文名称
cis,cis,cis-2,5,8-tribenzyltrindane-2,5,8-tricarboxylic acid
英文别名
——
cis,cis,cis-2,5,8-tribenzyltrindane-2,5,8-tricarboxylic acid化学式
CAS
410074-26-9
化学式
C39H36O6
mdl
——
分子量
600.711
InChiKey
BROUXQXAEDMAFS-CQWHFZLFSA-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):
    5.92
  • 重原子数:
    45.0
  • 可旋转键数:
    9.0
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    111.9
  • 氢给体数:
    3.0
  • 氢受体数:
    3.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • C <sub>3v</sub>-symmetric anion receptors with guanidine recognition motifs for ratiometric sensing of fluoride
    作者:Won Kim、Suban K. Sahoo、Gi-Dong Kim、Heung-Jin Choi
    DOI:10.1039/c5ra26039f
    日期:——
    Two new tripodal receptors 3 and 4 derived from a trindane framework having guanidine groups acting as hydrogen bond acceptors are synthesized and characterized for the selective recognition of anions. The anion recognition ability of the receptors was evaluated by UV-vis absorption, fluorescence and 1H NMR methods. Both the receptors showed F− selective ratiometric chromogenic and fluorogenic responses
    合成了两个新的三脚架受体3和4,它们来自具有基作为氢键受体的三丁烷骨架,并被表征用于选择性识别阴离子。通过紫外可见吸收,荧光和1 H NMR方法评估受体的阴离子识别能力。两个受体显示˚F -测试的阴离子中,由于主-客体复合,接着由所支持的酰胺- NH质子的抽象选择性比率显色和荧光反应1个1 H NMR滴定研究。受体4与荧光单位表明较大的f -比受体选择性3通过给予视觉上可检测的蓝色荧光和显著开启在其可以通过连续加入F的切换来回410nm的荧光-和H +。此外,可逆和可再现的4的荧光状态可用于设计以二进制逻辑形式显示“写-读-擦除-读”功能的分子级顺序存储单元。
  • A novel C3v-symmetric molecular clip with tris(diamide) recognition sites on trindane platform for H2PO4− recognition
    作者:Gi-Dong Kim、Shilpa Bothra、Suban K. Sahoo、Heung-Jin Choi
    DOI:10.1016/j.tetlet.2018.03.055
    日期:2018.4
    To avoid the deprotonation events occurred in the receptor upon recognition of basic anions, a novel C-3v-symmetric anion receptor 2 with two amide groups appended in each arm was designed and synthesized by using the trindane tricarboxylic acid as tripodal molecular framework. The anion recognition ability by 2 was examined by H-1 NMR titration study in DMSO-d(6), which revealed that the addition of H2PO4 guests caused substantial downfield shifts of the amide-NH protons peaks due to the formation of a host-guest complex in 1:1 binding stoichiometry with the estimated binding constant (K-a) of 244 M-1. No noticeable binding of 2 was observed with other tested anions such as F-, Cl-, Br-, I-, NO3- and HSO4- under similar conditions. (C) 2018 Elsevier Ltd. All rights reserved.
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