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N-(4-((E)-2-(4-bromonaphthalen-1-yl)vinyl)phenyl)-4-((E)-2-(4-((E)-2-(pyridin-4-yl)vinyl)naphthalen-1-yl)vinyl)-N-(4-((E)-2-(4-((E)-2-(pyridin-4-yl)vinyl)naphthalen-1-yl)vinyl)phenyl)benzenamide | 1246751-65-4

中文名称
——
中文别名
——
英文名称
N-(4-((E)-2-(4-bromonaphthalen-1-yl)vinyl)phenyl)-4-((E)-2-(4-((E)-2-(pyridin-4-yl)vinyl)naphthalen-1-yl)vinyl)-N-(4-((E)-2-(4-((E)-2-(pyridin-4-yl)vinyl)naphthalen-1-yl)vinyl)phenyl)benzenamide
英文别名
N-[4-[(E)-2-(4-bromonaphthalen-1-yl)ethenyl]phenyl]-4-[(E)-2-[4-[(E)-2-pyridin-4-ylethenyl]naphthalen-1-yl]ethenyl]-N-[4-[(E)-2-[4-[(E)-2-pyridin-4-ylethenyl]naphthalen-1-yl]ethenyl]phenyl]aniline
N-(4-((E)-2-(4-bromonaphthalen-1-yl)vinyl)phenyl)-4-((E)-2-(4-((E)-2-(pyridin-4-yl)vinyl)naphthalen-1-yl)vinyl)-N-(4-((E)-2-(4-((E)-2-(pyridin-4-yl)vinyl)naphthalen-1-yl)vinyl)phenyl)benzenamide化学式
CAS
1246751-65-4
化学式
C68H48BrN3
mdl
——
分子量
987.053
InChiKey
NBGZPORTPJCWAP-ZUDDTQOOSA-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):
    18.8
  • 重原子数:
    72
  • 可旋转键数:
    13
  • 环数:
    11.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    29
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    4-乙烯基吡啶 、 tris(4-(2-(4-bromonaphthalen-1-yl)vinyl)phenyl)amine 在 palladium diacetate 、 三乙胺三(邻甲基苯基)磷 作用下, 以 乙腈 为溶剂, 以46%的产率得到N-(4-((E)-2-(4-bromonaphthalen-1-yl)vinyl)phenyl)-4-((E)-2-(4-((E)-2-(pyridin-4-yl)vinyl)naphthalen-1-yl)vinyl)-N-(4-((E)-2-(4-((E)-2-(pyridin-4-yl)vinyl)naphthalen-1-yl)vinyl)phenyl)benzenamide
    参考文献:
    名称:
    Novel D–π3–(A)1–3 multibranched chromophores as an efficient two-photon-induced polymerization initiator
    摘要:
    The ability of novel branched chromophores that contained a triphenylamine group as donor, naphthalene as pi-bridge and pyridyl as acceptor group, to act as two-photon absorption and two-photon induced polymerization initiators were investigated Linear and nonlinear optical spectra revealed that chromophores with large dipolar moment change gave strong intramolecular charge-transfer characteristics that exhibited enhanced two-photon absorption cross-section A variety of micro-objects were fabricated, using an acrylate matrix, that contained the novel chromophores as two-photon induced polymerization initiator Molecular energy levels, electrochemistry and linear absorption spectra, as well as one-photon fluorescence quenching measurements supported the hypothesis that two-photon induced polymerization proceeds via intermolecular charge-transfer from initiator to monomer and, that the chromophore firstly generates the exciton via two-photon absorption and then transfers charge to the acrylate monomer which then polymerises (C) 2010 Elsevier Ltd. All rights reserved
    DOI:
    10.1016/j.dyepig.2010.05.001
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文献信息

  • Novel D–π3–(A)1–3 multibranched chromophores as an efficient two-photon-induced polymerization initiator
    作者:Xiaomei Wang、Feng Jin、Weizhou Zhang、Xutang Tao、Xuan-Ming Duan、Minhua Jiang
    DOI:10.1016/j.dyepig.2010.05.001
    日期:2011.1
    The ability of novel branched chromophores that contained a triphenylamine group as donor, naphthalene as pi-bridge and pyridyl as acceptor group, to act as two-photon absorption and two-photon induced polymerization initiators were investigated Linear and nonlinear optical spectra revealed that chromophores with large dipolar moment change gave strong intramolecular charge-transfer characteristics that exhibited enhanced two-photon absorption cross-section A variety of micro-objects were fabricated, using an acrylate matrix, that contained the novel chromophores as two-photon induced polymerization initiator Molecular energy levels, electrochemistry and linear absorption spectra, as well as one-photon fluorescence quenching measurements supported the hypothesis that two-photon induced polymerization proceeds via intermolecular charge-transfer from initiator to monomer and, that the chromophore firstly generates the exciton via two-photon absorption and then transfers charge to the acrylate monomer which then polymerises (C) 2010 Elsevier Ltd. All rights reserved
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