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1-(2-bromophenyl)-2-(3-bromophenyl)ethene

中文名称
——
中文别名
——
英文名称
1-(2-bromophenyl)-2-(3-bromophenyl)ethene
英文别名
2,3'-(ethene-1,2-diyl)bis(bromobenzene);1-Bromo-2-[2-(3-bromophenyl)ethenyl]benzene
1-(2-bromophenyl)-2-(3-bromophenyl)ethene化学式
CAS
——
化学式
C14H10Br2
mdl
——
分子量
338.041
InChiKey
JLQYSGUXZCLDAR-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):
    5.6
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    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:
    描述:
    1-(2-bromophenyl)-2-(3-bromophenyl)ethene 作用下, 以 甲苯 为溶剂, 以0.9 g的产率得到trans-1-(2-bromophenyl)-2-(3-bromophenyl)ethene
    参考文献:
    名称:
    Ferromagnetic Spin Alignment in Head-to-Tail Coupled Oligo(1,4-phenyleneethynylene)s and Oligo(1,4-phenylenevinylene)s Bearing Pendant p-Phenylenediamine Radical Cations
    摘要:
    The intramolecular and long-range ferromagnetic coupling between p-phenylenediamine radical cations in head-to-tail coupled oligo(1,4-phenyleneethynylene)s and oligo(1,4-phenylenvinylene)s between neighbors and next-nearest neighbors is described. UV/vis/near-IR experiments show that the radical cations are localized in the pendant p-phenylenediamine units of the conjugated oligomers. The ESR spectra of these oligo(1,4-phenyleneethynylene) and oligo(1,4-phenylenvinylene) di(radical cation)s are consistent with those of a triplet state. A linear behavior is observed for the doubly integrated ESR intensity of the Delta M-s = +/-1 and Delta M-s = +/-2 signals with the inverse temperature (I similar to 1/T), consistent with Curie's law. This behavior indicates a triplet ground-state diradical with a large triplet-singlet energy gap or possibly a degeneracy of singlet and triplet states.
    DOI:
    10.1021/jo000548o
  • 作为产物:
    描述:
    3-溴苄溴 在 sodium hydride 作用下, 以 四氢呋喃 为溶剂, 反应 15.0h, 生成 1-(2-bromophenyl)-2-(3-bromophenyl)ethene
    参考文献:
    名称:
    신규 페난트렌 화합물, 이의 제조방법 및 이를 이용한 유기전자소자
    摘要:
    本发明涉及一种具有优异发光效率和寿命的新型苯并噻吩化合物,其制备方法以及包含该新型苯并噻吩化合物的有机电子器件。
    公开号:
    KR102006994B1
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文献信息

  • USE OF APPENDED DYES IN OPTICAL DATA STORAGE MEDIA
    申请人:Natarajan Arunkumar
    公开号:US20120052232A1
    公开(公告)日:2012-03-01
    The present disclosure relates to optical media and the formation and use of such media. In certain embodiments the optical media or a composition suitable for such media includes a polymeric matrix or substrate. A dye, such as an energy transfer dye is chemically appended to the polymeric matrix or substrate, such as by one or more covalent bonds.
  • US5521160A
    申请人:——
    公开号:US5521160A
    公开(公告)日:1996-05-28
  • 신규 페난트렌 화합물, 이의 제조방법 및 이를 이용한 유기전자소자
    申请人:SAMYANG CORPORATION 주식회사 삼양사(120110515934) Corp. No ▼ 110111-4720945BRN ▼101-86-66838
    公开号:KR102006994B1
    公开(公告)日:2019-08-02
    본 발명은 발광효율과 수명이 우수한 신규 페난트렌 화합물, 그의 제조방법 및 상기 신규 페난트렌 화합물을 포함하는 유기전기소자가 개시된다.
    本发明涉及一种具有优异发光效率和寿命的新型苯并噻吩化合物,其制备方法以及包含该新型苯并噻吩化合物的有机电子器件。
  • Ferromagnetic Spin Alignment in Head-to-Tail Coupled Oligo(1,4-phenyleneethynylene)s and Oligo(1,4-phenylenevinylene)s Bearing Pendant <i>p</i>-Phenylenediamine Radical Cations
    作者:Pauline J. van Meurs、René A. J. Janssen
    DOI:10.1021/jo000548o
    日期:2000.9.1
    The intramolecular and long-range ferromagnetic coupling between p-phenylenediamine radical cations in head-to-tail coupled oligo(1,4-phenyleneethynylene)s and oligo(1,4-phenylenvinylene)s between neighbors and next-nearest neighbors is described. UV/vis/near-IR experiments show that the radical cations are localized in the pendant p-phenylenediamine units of the conjugated oligomers. The ESR spectra of these oligo(1,4-phenyleneethynylene) and oligo(1,4-phenylenvinylene) di(radical cation)s are consistent with those of a triplet state. A linear behavior is observed for the doubly integrated ESR intensity of the Delta M-s = +/-1 and Delta M-s = +/-2 signals with the inverse temperature (I similar to 1/T), consistent with Curie's law. This behavior indicates a triplet ground-state diradical with a large triplet-singlet energy gap or possibly a degeneracy of singlet and triplet states.
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