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6,15-hexacenequinone | 13214-71-6

中文名称
——
中文别名
——
英文名称
6,15-hexacenequinone
英文别名
6,15-hexacenedione;hexacene-6,15-dione;Hexacen-6,15-dion;Hexacen-6,15-chinon;Hexacen-chinon-6,15
6,15-hexacenequinone化学式
CAS
13214-71-6
化学式
C26H14O2
mdl
——
分子量
358.396
InChiKey
MGVJQYXHFHWDRW-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

物化性质

  • 沸点:
    634.6±25.0 °C(Predicted)
  • 密度:
    1.370±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.6
  • 重原子数:
    28
  • 可旋转键数:
    0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    6,15-hexacenequinone盐酸 、 tin(ll) chloride 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 反应 7.0h, 生成 6,15-diphenylhexacene
    参考文献:
    名称:
    重新审视六边形的稳定性。
    摘要:
    使用Strating-Zwanenberg光脱羰基反应制备并六苯(1)。发现化合物1在溶液中极不稳定,经历二聚化和氧化。但是,当在聚合物基质中生成1时,在环境条件下可存活超过12小时。使用醌还原法合成了在6和15位上被苯基,对叔丁基苯基和三甲苯基取代的己烯,但这些化合物在溶液中也不稳定。
    DOI:
    10.1021/ol0709376
  • 作为产物:
    参考文献:
    名称:
    The preparation and reactions of naphtho[1,2-c]furan and naphtho[2,3-c]furan
    摘要:
    DOI:
    10.1021/jo00370a004
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文献信息

  • Functionalized Higher Acenes:  Hexacene and Heptacene
    作者:Marcia M. Payne、Sean R. Parkin、John E. Anthony
    DOI:10.1021/ja051798v
    日期:2005.6.1
    We have extended our functionalization strategy for pentacene to the higher acenes hexacene and heptacene. Provided a large enough alkyne substituent is used, these large aromatic rods are both stable and soluble and can be characterized spectroscopically as well as by single-crystal X-ray diffraction.
    我们已将并五苯的功能化策略扩展到更高级的并苯六苯和七苯。如果使用足够大的炔烃取代基,这些大芳烃棒既稳定又可溶,并且可以通过光谱和单晶 X 射线衍射进行表征。
  • DIOXAANTHANTHRENE-BASED COMPOUND, LAMINATED STRUCTURE AND MOLDING METHOD THEREOF, AND ELECTRONIC DEVICE AND PRODUCTION METHOD THEREOF
    申请人:Sony Corporation
    公开号:EP2767540A1
    公开(公告)日:2014-08-20
    Provided is a dioxaanthanthrene compound represented by, for example, the following structural formula (1).
    提供的是一种二氧蒽化合物,例如,可以用以下结构式(1)表示。
  • Synthesis and Stability of Soluble Hexacenes
    作者:Balaji Purushothaman、Sean R. Parkin、John E. Anthony
    DOI:10.1021/ol100178s
    日期:2010.5.7
    The synthesis of new silylethyne-substituted hexacene derivatives to investigate their solubility, stability, and π-stacking is reported. It was found that “butterfly” dimerization, rather than photooxidation, is the dominant decomposition pathway for these molecules and that stability can be enhanced by functionalization to prevent close contact between specific regions of the aromatic core. Dimerization
    报道了合成新的甲硅烷基乙炔取代的并六苯衍生物以研究其溶解性,稳定性和π堆积的方法。发现“蝴蝶”二聚而不是光氧化是这些分子的主要分解途径,并且可以通过官能化防止芳族核的特定区域之间的紧密接触来增强稳定性。二聚体区域选择性可以通过适当地设计生色团的固态排列来改变。
  • ORGANIC SEMICONDUCTOR COMPOSITION, ORGANIC SEMICONDUCTOR ELEMENT, AND PROCESS FOR PRODUCING THE SAME
    申请人:KONICA CORPORATION
    公开号:EP1498456A1
    公开(公告)日:2005-01-19
    Disclosed is an organic semiconductor composition containing particles and an organic semiconducting compound combining with the particles.
    公开了一种有机半导体组合物,其中含有颗粒和与颗粒结合的有机半导体化合物。
  • RESIN COMPOSITION FOR PRINTING PLATE
    申请人:Asahi Kasei Chemicals Corporation
    公开号:EP2100907A1
    公开(公告)日:2009-09-16
    Disclosed is a polymer having excellent solvent resistance which can be produced by using a polycarbonate diol having a repeating unit represented by the formula (1) and/or (2), having a hydroxyl group at both termini, and having a number average molecular weight of from 300 to 50,000: wherein R1 represents a linear or branched hydrocarbon group having 2 to 50 carbon atoms; and n represents an integer of 2 to 50, wherein R2 represents a linear or branched hydrocarbon group having 10 to 50 carbon atoms.
    本发明公开了一种具有优异耐溶剂性的聚合物,该聚合物可通过使用一种聚碳酸酯二元醇来生产,该二元醇具有由式(1)和/或(2)表示的重复单元,其两个末端均带有羟基,且平均分子量在 300 至 50,000 之间: 其中 R1 代表具有 2 至 50 个碳原子的线性或支链烃基;n 代表 2 至 50 的整数、 其中 R2 代表具有 10 至 50 个碳原子的直链或支链烃基。
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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