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1,4-Bis(2-(4-methylphenyl)-vinyl)-2,5-dimethoxy-benzol | 10273-66-2

中文名称
——
中文别名
——
英文名称
1,4-Bis(2-(4-methylphenyl)-vinyl)-2,5-dimethoxy-benzol
英文别名
4,4'-(2,5-dimethoxy-1,4-phenylene)bis(ethene-2,1-diyl)bis(methylbenzene);2,5-dimethoxy-1,4-bis[(E)-2-(4-methylphenyl)ethenyl]benzene;1,4-dimethoxy-2,5-bis[(E)-2-(4-methylphenyl)ethenyl]benzene
1,4-Bis(2-(4-methylphenyl)-vinyl)-2,5-dimethoxy-benzol化学式
CAS
10273-66-2
化学式
C26H26O2
mdl
——
分子量
370.491
InChiKey
GEBXCURGGONPOB-WXUKJITCSA-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:
    28
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

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

  • 作为反应物:
    描述:
    甲醇1,4-Bis(2-(4-methylphenyl)-vinyl)-2,5-dimethoxy-benzol氢氧化钾 作用下, 以 四氢呋喃 为溶剂, 反应 3.0h, 以51.3%的产率得到3,3,6,6-tetramethoxy-1,4-bis<2-(4-methylphenyl)vinyl>cyclohexa-1,4-diene
    参考文献:
    名称:
    Irngartinger, Hermann; Lichtenthaeler, Jochen; Fenske, Dieter, Zeitschrift fur Naturforschung, B: Chemical Sciences, 1993, vol. 48, # 10, p. 1411 - 1418
    摘要:
    DOI:
  • 作为产物:
    参考文献:
    名称:
    Plastic Scintillators. II. The Synthesis of Some Distyrylbenzene Derivatives as Wavelength Shifters in Plastic Scintillators
    摘要:
    报告了2, 5-二甲氧基-1, 4-二苯乙烯衍生物及相关化合物的合成、吸收和荧光光谱。随后讨论了它们的吸收和荧光光谱。根据光谱数据,本文合成的部分化合物在塑料闪烁体中作为波长移变器的性能优于文献中描述的化合物。
    DOI:
    10.1246/bcsj.39.1547
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文献信息

  • Phenylenevinylene oligomers by Mizoroki-Heck cross coupling reaction. Structural and optoelectronic characterization
    作者:Sandra E. Estrada、Cristian Ochoa-Puentes、Cesar A. Sierra
    DOI:10.1016/j.molstruc.2016.12.032
    日期:2017.4
    spectroscopies. The results showed that, with only one exception, the ED and EW groups at the ends of OPV systems lead to a bathochromic shift. This effect is intensified with the introduction of methoxy groups on the central ring. Consistent with these, the HOMO-LUMO gaps (ΔE) decreases as the strength of ED and EW substituents increases. The ED and EW substituents also lead to a decrease in the Φ f values
    摘要 为了研究分子结构对全反式亚苯基亚乙烯基低聚物 (OPV) 光学性质的影响,16 种 1,4-二苯乙烯基苯衍生物( 1a-i 和 2a-g )具有不同的给电子(ED)功能。 ) 和吸电子 (EW) 基团通过 Mizoroki-Heck 交叉偶联反应以中等至良好的产率(40-95%)合成。所实施的方法,经过我们小组先前报道的小改动,可以获得所需的乙烯基构型以及一种新型 OPV 化合物 (1h)。在通过几种技术(例如 FTIR、 1 H、 13 C 和固态核磁共振)进行结构表征后,特别强调通过紫外-可见光和荧光光谱研究它们的光学特性。结果表明,除了一个例外,OPV 系统末端的 ED 和 EW 组导致红移。随着在中心环上引入甲氧基,这种效果得到加强。与这些一致,HOMO-LUMO 间隙(ΔE)随着 ED 和 EW 取代基强度的增加而减小。ED 和 EW 取代基也会导致 Φ f 值降低。这种在
  • One-pot synthesis and study of spectroscopic properties of oligo(phenylenevinylene)s
    作者:Krupa N. Patel、Ashutosh V. Bedekar
    DOI:10.1016/j.tetlet.2015.10.033
    日期:2015.11
    Two series of OPVs (oligo(phenylenevinylene)), that is, ((1E,1'E)-(2,5-dimethoxy-1,4-phenylene)bis (ethene-2,1-diyl))dibenzene derivatives and 4-((E)-4-((E)-styryl)styryl)pyridine derivatives with different functional groups of varying electronic properties have been synthesized by one-pot Wittig-Heck methodology. The synthesized derivatives have been studied for their optical properties. Amongst them the ((1E,1'E)-(2,5-dimethoxy-1,4-phenylene)bis(ethene-2,1-diyl))dibenzene derivatives with appropriate changes in the end group showed a significant impact on the UV absorption and emission spectra. Particularly NO2-OPV showed distinct solvatochromism in the wavelength range of 218 nm in different solvents. Whereas 4-((E)-4((E)-styryl)styryl)pyridine derivatives showed clear acidochromism which can be detected visually as well as spectroscopically. (C) 2015 Elsevier Ltd. All rights reserved.
  • Solid State Behaviour of Vinyl Quinones
    作者:Hermann Irngartinger、Jochen Lichtenthäler、Rüdiger Herpich、Birgit Stadler
    DOI:10.1080/10587259608039394
    日期:1996.2
    2,5-Bisvinyl-1,4-benzoquinones 1 and 2-vinyl-1,4-benzoquinones 2 substituted with aryl or ester end groups have been synthesized. The 2,5-bisstyryl-1,4-benzoquinones 1 (R=phenyl, p-tolyl, o-tolyl) crystallize with a 7 Angstrom-stacking axis. But only for the o-tolyl derivative the contacts between the vinyl groups are close enough to allow a four-center type photopolymerization. The ester derivative 1 (R=COOEt) has a layer structure and can be photooligomerized in the crystal. The generated cyclobutane subgroups have twofold symmetry. The vinylquinones 2 (R=aryl) may be dimerized photochemically in the crystal at the vinyl groups to centrosymmetric cyclobutanes. Crystals with 4 Angstrom stacking axis are also photoreactive.
  • PHOTOSENSITIVE RESIN COMPOSITION, PHOTOSENSITIVE ELEMENT, CURED PRODUCT, SEMICONDUCTOR DEVICE, METHOD FOR FORMING RESIST PATTERN, AND METHOD FOR PRODUCING CIRCUIT SUBSTRATE
    申请人:Hitachi Chemical Company, Ltd.
    公开号:US20170329220A1
    公开(公告)日:2017-11-16
    A photosensitive resin composition comprises: a resin having a phenolic hydroxyl group; a photosensitive acid generator; a compound having at least one selected from the group consisting of an aromatic ring, a heterocycle and an alicycle, and at least one selected from the group consisting of a methylol group and an alkoxyalkyl group; an aliphatic compound having two or more functional groups being at least one selected from the group consisting of an acryloyloxy group, a methacryloyloxy group, a glycidyloxy group, an oxetanyl alkyl ether group, a vinyl ether group and a hydroxyl group; and a compound having at least one skeleton selected from the group consisting of an anthracene skeleton, a phenanthrene skeleton, a pyrene skeleton, a perylene skeleton, a carbazole skeleton, a phenothiazine skeleton, a xanthone skeleton, a thioxanthone skeleton, an acridine skeleton, a phenylpyrazoline skeleton, a distyrylbenzene skeleton and a distyrylpyridine skeleton, or a benzophenone compound.
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