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4-(1,10-phenanthrolin-5-yl)aniline | 1334286-49-5

中文名称
——
中文别名
——
英文名称
4-(1,10-phenanthrolin-5-yl)aniline
英文别名
——
4-(1,10-phenanthrolin-5-yl)aniline化学式
CAS
1334286-49-5
化学式
C18H13N3
mdl
——
分子量
271.321
InChiKey
BPZQQISYIBJEFA-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

物化性质

  • 沸点:
    478.8±40.0 °C(Predicted)
  • 密度:
    1.281±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.03
  • 重原子数:
    21.0
  • 可旋转键数:
    1.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    51.8
  • 氢给体数:
    1.0
  • 氢受体数:
    3.0

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    A Heterobimetallic Ruthenium–Gadolinium Complex as a Potential Agent for Bimodal Imaging
    摘要:
    Trinuclear heterobimetallic Ln(III)-Ru-II cornplexes (Ln = Eu, Gd) based on a 1,10-phenanthroline ligand bearing a diethylenetriaminepentaacetic acid (DTPA) core have been synthesized and fully characterized by a range of experimental techniques. The O-17 NMR and proton nuclear magetic relaxation dispersion (NMRD) measurements of Gd-III-Ru-II show that, in comparison to the parent Gd-DTPA, this complex exhibits improved relaxivity, which is the result of an increase of the rotational correlation time. Relaxometry and ultrafiltration experiments indicate that the 1,10-phenanthroline ligand has a high affinity for noncovalent binding to human serum albumin, which results in a high relaxivity r(1) of 14.3 s(-1) mM(-1) at 20 MHz and 37 degrees C. Furthermore, the Ln(III)-Ru-II complexes (Ln = Eu, Gd) show an intense light absorption in the visible spectral region due to metal-to-ligand charge transfer (MLCT) transitions. Upon excitation into the MLCT band at 440 nm, the complexes exhibit a bright-red luminescence centered at 610 nm, with a quantum yield of 4.7%. The luminescence lifetime equals 540 ns and is therefore long enough to exceed the fluorescent background. Monometallic lanthanide complexes have also been synthesized, and the Eu-III analogue shows a characteristic red luminescence with a quantum yield of 0.8%. Taking into account the relaxometric and luminescent properties, the developed Gd-III-Ru-II complex can be considered as a potential in vitro bimodal imaging agent.
    DOI:
    10.1021/ic200726t
  • 作为产物:
    描述:
    tert-butyl [4-(1,10-phenanthrolin-5-yl)phenyl]carbamate三氟乙酸 作用下, 以 二氯甲烷 为溶剂, 以81%的产率得到4-(1,10-phenanthrolin-5-yl)aniline
    参考文献:
    名称:
    A Heterobimetallic Ruthenium–Gadolinium Complex as a Potential Agent for Bimodal Imaging
    摘要:
    Trinuclear heterobimetallic Ln(III)-Ru-II cornplexes (Ln = Eu, Gd) based on a 1,10-phenanthroline ligand bearing a diethylenetriaminepentaacetic acid (DTPA) core have been synthesized and fully characterized by a range of experimental techniques. The O-17 NMR and proton nuclear magetic relaxation dispersion (NMRD) measurements of Gd-III-Ru-II show that, in comparison to the parent Gd-DTPA, this complex exhibits improved relaxivity, which is the result of an increase of the rotational correlation time. Relaxometry and ultrafiltration experiments indicate that the 1,10-phenanthroline ligand has a high affinity for noncovalent binding to human serum albumin, which results in a high relaxivity r(1) of 14.3 s(-1) mM(-1) at 20 MHz and 37 degrees C. Furthermore, the Ln(III)-Ru-II complexes (Ln = Eu, Gd) show an intense light absorption in the visible spectral region due to metal-to-ligand charge transfer (MLCT) transitions. Upon excitation into the MLCT band at 440 nm, the complexes exhibit a bright-red luminescence centered at 610 nm, with a quantum yield of 4.7%. The luminescence lifetime equals 540 ns and is therefore long enough to exceed the fluorescent background. Monometallic lanthanide complexes have also been synthesized, and the Eu-III analogue shows a characteristic red luminescence with a quantum yield of 0.8%. Taking into account the relaxometric and luminescent properties, the developed Gd-III-Ru-II complex can be considered as a potential in vitro bimodal imaging agent.
    DOI:
    10.1021/ic200726t
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