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1,3-bis(8-(p-nitrophenylaminocarbonylamino)-3,6-di-tertbutyl-9H-carbazol-1-yl)urea

中文名称
——
中文别名
——
英文名称
1,3-bis(8-(p-nitrophenylaminocarbonylamino)-3,6-di-tertbutyl-9H-carbazol-1-yl)urea
英文别名
1,3-bis[3,6-ditert-butyl-8-[(4-nitrophenyl)carbamoylamino]-9H-carbazol-1-yl]urea
1,3-bis(8-(p-nitrophenylaminocarbonylamino)-3,6-di-tertbutyl-9H-carbazol-1-yl)urea化学式
CAS
——
化学式
C55H60N10O7
mdl
——
分子量
973.144
InChiKey
DUUZHHSPYODOLC-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):
    12.9
  • 重原子数:
    72
  • 可旋转键数:
    10
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    247
  • 氢给体数:
    8
  • 氢受体数:
    7

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

  • 作为产物:
    描述:
    3,6-二叔丁基咔唑 在 palladium on activated charcoal 、 硝酸乙酸酐溶剂黄146三氟乙酸 作用下, 以 四氢呋喃乙醇二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 6.0h, 生成 1,3-bis(8-(p-nitrophenylaminocarbonylamino)-3,6-di-tertbutyl-9H-carbazol-1-yl)urea
    参考文献:
    名称:
    Bis(carbazolyl)ureas as Selective Receptors for the Recognition of Hydrogenpyrophosphate in Aqueous Media
    摘要:
    Recognition properties of the novel bis(carbazole) tris-ureidic-based receptors 1 and 2 toward different anions have been studied by H-1 NMR and absorption and emission spectroscopy, as well as by DFT calculations. Receptor 1, in which the two urea-functionalized arms are decorated with p-nitrophenyl rings, behaves as a highly selective chromogenic molecular probe for hydrogenpyrophosphate anion in a competitive medium (acetonitrile/water, 70/30). Receptor 2, bearing two urea arms decorated with photoactive pyrenyl rings, acts as a highly selective fluorescent molecular probe for hydrogenpyrophosphate anion in either acetonitrile or an aqueous mixture (acetonitrile/water, 85/15). Receptor 2 exhibits a dual monomer-excimer emission spectrum and undergoes a remarked ratiometry in acetonitrile in the presence of hydrogenpyrophosphate: the excimer band disappears, whereas the monomer band is slightly increased. However, in the aqueous mixture, a strong increase of the excimer emission band was observed, while the monomer emission bands remained almost unaffected. The resulting binding modes and spectroscopic features are explained by suitable structures of model complexes for both receptors. In such complexes, a peripheral cooperative effect was found, alleviating the excess of negative charge in the guest toward the outer surface of the host, as well as the required enlargement on its internal cavity.
    DOI:
    10.1021/jo401430d
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文献信息

  • Bis(carbazolyl)ureas as Selective Receptors for the Recognition of Hydrogenpyrophosphate in Aqueous Media
    作者:Guzman Sanchez、Arturo Espinosa、David Curiel、Alberto Tarraga、Pedro Molina
    DOI:10.1021/jo401430d
    日期:2013.10.4
    Recognition properties of the novel bis(carbazole) tris-ureidic-based receptors 1 and 2 toward different anions have been studied by H-1 NMR and absorption and emission spectroscopy, as well as by DFT calculations. Receptor 1, in which the two urea-functionalized arms are decorated with p-nitrophenyl rings, behaves as a highly selective chromogenic molecular probe for hydrogenpyrophosphate anion in a competitive medium (acetonitrile/water, 70/30). Receptor 2, bearing two urea arms decorated with photoactive pyrenyl rings, acts as a highly selective fluorescent molecular probe for hydrogenpyrophosphate anion in either acetonitrile or an aqueous mixture (acetonitrile/water, 85/15). Receptor 2 exhibits a dual monomer-excimer emission spectrum and undergoes a remarked ratiometry in acetonitrile in the presence of hydrogenpyrophosphate: the excimer band disappears, whereas the monomer band is slightly increased. However, in the aqueous mixture, a strong increase of the excimer emission band was observed, while the monomer emission bands remained almost unaffected. The resulting binding modes and spectroscopic features are explained by suitable structures of model complexes for both receptors. In such complexes, a peripheral cooperative effect was found, alleviating the excess of negative charge in the guest toward the outer surface of the host, as well as the required enlargement on its internal cavity.
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