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1,3-bis((4-(pyridin-3-yl)phenyl)ethynyl)benzene | 1333334-22-7

中文名称
——
中文别名
——
英文名称
1,3-bis((4-(pyridin-3-yl)phenyl)ethynyl)benzene
英文别名
1,3-bis((4-(pyridin-3-yl)phenyl)enyl)benzene;3-[4-[2-[3-[2-(4-Pyridin-3-ylphenyl)ethynyl]phenyl]ethynyl]phenyl]pyridine;3-[4-[2-[3-[2-(4-pyridin-3-ylphenyl)ethynyl]phenyl]ethynyl]phenyl]pyridine
1,3-bis((4-(pyridin-3-yl)phenyl)ethynyl)benzene化学式
CAS
1333334-22-7
化学式
C32H20N2
mdl
——
分子量
432.524
InChiKey
IJMKVGAVXWBUDQ-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):
    7.1
  • 重原子数:
    34
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    25.8
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    Pd(OTf)21,3-bis((4-(pyridin-3-yl)phenyl)ethynyl)benzene二甲基亚砜 为溶剂, 生成 [(1,3-bis((4-pyridin-3-yl)phenyl)ethynyl)benzene)4Pd2](OTf)4
    参考文献:
    名称:
    Synthesis and Properties of Metal–Ligand Complexes with Endohedral Amine Functionality
    摘要:
    A series of tetracationic M2L4 palladium-pyridyl complexes with endohedral amine functionality have been synthesized. The complexes were analyzed by NMR techniques (including Diffusion NMR and 2D NOESY), electrospray ionization (ESI) mass spectrometry, and X-ray crystallography. The solid state analysis shows a large change in crystal morphology upon introduction of the endohedral amine groups, caused by deleterious interactions between the amines and the triflate counterions from the coordination process. Combination of different ligands allows analysis of ligand exchange rates via NMR analysis, with half-lives on the order of 3 h, independent of the donor properties of the ligand. Self-sorting behavior is observed, with more electron-rich ligands being favored. The amine-containing and extended complexes are strongly fluorescent, giving quantum yields of up to 83%.
    DOI:
    10.1021/ic201092s
  • 作为产物:
    描述:
    对溴碘苯1,3-二乙炔苯 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodidecaesium carbonate二异丙胺 作用下, 以 乙醇甲苯 为溶剂, 反应 54.0h, 生成 1,3-bis((4-(pyridin-3-yl)phenyl)ethynyl)benzene
    参考文献:
    名称:
    Synthesis and Properties of Metal–Ligand Complexes with Endohedral Amine Functionality
    摘要:
    A series of tetracationic M2L4 palladium-pyridyl complexes with endohedral amine functionality have been synthesized. The complexes were analyzed by NMR techniques (including Diffusion NMR and 2D NOESY), electrospray ionization (ESI) mass spectrometry, and X-ray crystallography. The solid state analysis shows a large change in crystal morphology upon introduction of the endohedral amine groups, caused by deleterious interactions between the amines and the triflate counterions from the coordination process. Combination of different ligands allows analysis of ligand exchange rates via NMR analysis, with half-lives on the order of 3 h, independent of the donor properties of the ligand. Self-sorting behavior is observed, with more electron-rich ligands being favored. The amine-containing and extended complexes are strongly fluorescent, giving quantum yields of up to 83%.
    DOI:
    10.1021/ic201092s
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文献信息

  • Synthesis and Properties of Metal–Ligand Complexes with Endohedral Amine Functionality
    作者:Amber M. Johnson、Orly Moshe、Ana S. Gamboa、Brian W. Langloss、John F. K. Limtiaco、Cynthia K. Larive、Richard J. Hooley
    DOI:10.1021/ic201092s
    日期:2011.10.3
    A series of tetracationic M2L4 palladium-pyridyl complexes with endohedral amine functionality have been synthesized. The complexes were analyzed by NMR techniques (including Diffusion NMR and 2D NOESY), electrospray ionization (ESI) mass spectrometry, and X-ray crystallography. The solid state analysis shows a large change in crystal morphology upon introduction of the endohedral amine groups, caused by deleterious interactions between the amines and the triflate counterions from the coordination process. Combination of different ligands allows analysis of ligand exchange rates via NMR analysis, with half-lives on the order of 3 h, independent of the donor properties of the ligand. Self-sorting behavior is observed, with more electron-rich ligands being favored. The amine-containing and extended complexes are strongly fluorescent, giving quantum yields of up to 83%.
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