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2,3-Bis(4-hexoxyphenyl)pentacene-6,13-dione | 1610474-45-7

中文名称
——
中文别名
——
英文名称
2,3-Bis(4-hexoxyphenyl)pentacene-6,13-dione
英文别名
2,3-bis(4-hexoxyphenyl)pentacene-6,13-dione
2,3-Bis(4-hexoxyphenyl)pentacene-6,13-dione化学式
CAS
1610474-45-7
化学式
C46H44O4
mdl
——
分子量
660.853
InChiKey
FEIMACKVRDDIGM-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):
    13.2
  • 重原子数:
    50
  • 可旋转键数:
    14
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    2,3-Bis(4-hexoxyphenyl)pentacene-6,13-dione丙二腈四氯化钛 作用下, 以 吡啶二氯甲烷 为溶剂, 以43%的产率得到2-[13-(Dicyanomethylidene)-2,3-bis(4-hexoxyphenyl)pentacen-6-ylidene]propanedinitrile
    参考文献:
    名称:
    Pentacenequinone derivatives for preparation of gold nanoparticles: facile synthesis and catalytic application
    摘要:
    我们使用Suzuki-Miyaura偶联和Knoevenagel缩合协议,设计和合成了具有腈基的五环喹喔醌/五环喹喔二甲烷衍生物3、4和6。
    DOI:
    10.1039/c4ta00397g
  • 作为产物:
    描述:
    9,10-dibromo-6,13-pentacenequinone 、 4-己氧基苯硼酸频呢醇酯四(三苯基膦)钯potassium carbonate 作用下, 以 1,4-二氧六环 为溶剂, 以35%的产率得到2,3-Bis(4-hexoxyphenyl)pentacene-6,13-dione
    参考文献:
    名称:
    Pentacenequinone derivatives for preparation of gold nanoparticles: facile synthesis and catalytic application
    摘要:
    我们使用Suzuki-Miyaura偶联和Knoevenagel缩合协议,设计和合成了具有腈基的五环喹喔醌/五环喹喔二甲烷衍生物3、4和6。
    DOI:
    10.1039/c4ta00397g
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文献信息

  • Pentacenequinone derivatives: aggregation-induced emission enhancement, mechanism and fluorescent aggregates for superamplified detection of nitroaromatic explosives
    作者:Sandeep Kaur、Ankush Gupta、Vandana Bhalla、Manoj Kumar
    DOI:10.1039/c4tc01194e
    日期:——
    Suzuki–Miyaura coupling protocol. These derivatives form fluorescent aggregates in mixed aqueous media due to their aggregation-induced emission enhancement (AIEE) attributes. Interestingly, size dependent emission enhancement is observed in the case of derivatives 5–7 and the effect of increase in the number of pyridine rotors on fluorescence emission of pentacenequinone derivatives 6–7 in solution and
    并五苯醌衍生物5-9是通过Suzuki-Miyaura偶联方案合成的。这些衍生物由于其聚集诱导的发射增强(AIEE)属性,在混合的水性介质中形成了荧光聚集体。有趣的是,在衍生物5–7的情况下,观察到了尺寸依赖性的发射增强,并且吡啶转子数的增加对溶液中并处于聚集状态的并五苯醌衍生物6–7的荧光发射的影响证实了AIEE现象处于聚集的成本驱动生长并限制分子内旋转(RIR)。另一方面,导数8和9具有富电子苯基的施主-受主-施主类型的系统表现出分子间的电荷转移状态(ICT),并在混合的水性介质中形成荧光聚集体。除此之外,AIEE的特性还使并五苯醌衍生物5-9具有传感功能,例如检测硝基芳香族化合物。AIEE活性并五苯醌衍生物5–9的TLC条带为痕量硝基芳香族炸药的检测提供了一种更方便且更具成本效益的方法。
  • Pentacenequinone derivatives for preparation of gold nanoparticles: facile synthesis and catalytic application
    作者:Kamaldeep Sharma nee Kamaldeep、Sandeep Kaur、Vandana Bhalla、Manoj Kumar、Ankush Gupta
    DOI:10.1039/c4ta00397g
    日期:——

    We have designed and synthesized pentacenequinone/pentacenequinodimethane derivatives 3, 4 and 6 having nitrile groups using Suzuki–Miyaura coupling and Knoevenagel condensation protocols.

    我们使用Suzuki-Miyaura偶联和Knoevenagel缩合协议,设计和合成了具有腈基的五环喹喔醌/五环喹喔二甲烷衍生物3、4和6。
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同类化合物

6,13-五并苯醌 5,7,12,14-并五苯四酮 penta[2,3-b:9,10-b']dithiophene-6,14-dione 2,3,9,10-tetrakis(4-dodecyloxyphenylethynyl)-6,13-pentacenequinone 2,3,9,10-tetrachloropentacene-6,13-dione 2,9-bis(trifluoromethylsulfonyloxy)-6,13-pentacenequinone ethyl 7,14-dioxo-2-tosyl-1,2,3,4,7,14-hexahydrotetraceno[2,3-g]isoquinoline-3-carboxylate 2,9-bis(trifluoromethylsulfonyloxy)-5,7,12,14-pentacenediquinone 2,9-bis(triisopropylsilylethynyl)-5,7,12,14-pentacenediquinone 2,10-bis(trifluoromethylsulfonyloxy)-5,7,12,14-pentacenediquinone 2,10-bis(triisopropylsilylethynyl)-5,7,12,14-pentacenediquinone 2,3,9,10-tetramethoxycarbonylpentacene-6,13-quinone 2,3,9,10-tetramethyl-1,4,6,8,11,13-pentacenehexone 2,9-bis(trifluoromethylsulfonyloxy)-6,13-pentacenequinone 2,9-bis(triisopropylsilylethynyl)pentacene-6,13-dione 2,3-bis(di-N-phenylrhodamine B)-6,13-pentacenequinone 1,2,3,4,8,9,10,11-octafluoro-6,13-pentacenequinone 2,9-bis(tert-butyldimethylsilyloxy)pentacene-6,13-dione 2,9-bis(4-hexylthienyl)pentacene-6,13-dione 2,10-dibromo-pentacenequinone 2,9-dibromo-pentacenequinone 6,8,15,17-tetrakis-(p-tert-butylphenyl)-7,16-quinone 6,15-bis(p-tert-butylphenyl)-8,17-diphenyl-7,16-quinone 9,9,25,25-Tetraethyl-8,10,24,26-tetraoxaoctacyclo[15.15.0.03,15.05,13.07,11.019,31.021,29.023,27]dotriaconta-1(32),3(15),4,6,11,13,17,19,21,23(27),28,30-dodecaene-2,16-dione 2,9-dimethylpentacene-5,7,12,14-tetrone 8,19-bis(3,5-di-tert butyl phenyl)-6,10,17,21-nonacene tetraone 2,3-bis(dodecyloxy)pentacene-6,13-dione 1,2,3,4-tetrafluoropentacene-6,13-dione 5-(4-trifluoromethylphenyl)-14-phenylpentacene-6,13-dione 4-(6,13-dioxo-14-phenyl-6,13-dihydropentacen-5-yl)benzoic acid methyl ester 5-phenyl-14-(thiophen-2-yl)pentacene-6,13-dione 1-fluoropentacene-6,13-dione 2,9-bis(tert-butyldimethylsiloxy)-5,7,12,14-pentacenediquinone 2,10-bis(tert-butyldimethylsiloxy)-5,7,12,14-pentacenediquinone 2,9-difluoropentacene-5,7,12,14-tetrone 5,7,12,14-tetrakis(2-(triethylsilyl)ethyl)pentacene-6,13-dione 5,14-dimethoxypentacene-6,13-dione 6,8,15,17-tetraphenylheptacene-7,16-quinone 6,13-diphenyl-pentacene-5,7,12,14-tetraone 1,4,8,11-tetramethoxypentacene-6,13-dione 2,3-bis(4-((2-methoxynaphthalen-2-yl)-methyleneamino)phenyl)-6,13-pentacenequinone 1,4-diacetoxy-5,7,14,16-tetrakis(4-tert-butylphenyl)-6,8,13,15-hexacenetetrone heptacene-5,7,9,14,16,18-hexone 2,3-dimethylpentacene-6,13-dione 23,26,29,32,35,38-Hexaoxahexacyclo[20.16.0.03,20.05,18.07,16.09,14]octatriaconta-1,3,5(18),7,9,11,13,15,19,21-decaene-6,17-dione 1,2,3,4,8,12,13,14,15,19-deca(4'-t-butylphenylthio)nonacene-6,10,17,21-tetraone 5-(4-bromophenyl)-14-phenylpentacene-6,13-dione 5,9,14,18-tetrakis(4-(trifluoromethyl)phenyl)heptacene-7,16-dione 2-(methoxycarbonyl)-3-((methoxycarbonyl)methyl)-1,11,13-trimethoxy-5,7,12,14-pentacenediquinone 2-(N-phenylrhodamine B)-6,13-pentacenequinone