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1,2-bis(benzylsulfanyl)-1H-phenalene

中文名称
——
中文别名
——
英文名称
1,2-bis(benzylsulfanyl)-1H-phenalene
英文别名
——
1,2-bis(benzylsulfanyl)-1H-phenalene化学式
CAS
——
化学式
C27H22S2
mdl
——
分子量
410.6
InChiKey
NVSSXNARHHLNOO-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):
    7.4
  • 重原子数:
    29
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    50.6
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • [EN] 1-FUNCTIONALIZED DIBENZOFURANS AND DIBENZOTHIOPHENES FOR ORGANIC LIGHT EMITTING DIODES (OLEDS)<br/>[FR] DIBENZOTHIOPHÈNES ET DIBENZOFURANNES FONCTIONNALISÉS EN 1 POUR DIODES ÉLECTROLUMINESCENTES ORGANIQUES (OLED)
    申请人:IDEMITSU KOSAN CO
    公开号:WO2016097983A1
    公开(公告)日:2016-06-23
    The present invention relates to compounds of formula(I), a process for their production and their use in electronic devices, especially electroluminescent devices. When used as charge transport material and/or host material for phosphorescent emitters in electroluminescent devices, the compounds of formula I may provide improved efficiency and reduced driving voltage of electroluminescent devices.
    本发明涉及公式(I)化合物,其生产过程以及它们在电子设备中的应用,特别是电致发光设备。当作为电荷传输材料和/或磷光发射体在电致发光设备中的主体材料时,公式I的化合物可能提供电致发光设备的改进效率和降低驱动电压。
  • [EN] AZADIBENZOTHIOPHENES FOR ELECTRONIC APPLICATIONS<br/>[FR] AZADIBENZOTHIOPHÈNES POUR APPLICATIONS ÉLECTRONIQUES
    申请人:BASF SE
    公开号:WO2015063046A1
    公开(公告)日:2015-05-07
    The present invention relates to compounds of formula (I), which are characterized in that they are substituted by benzimidazo[1,2-a]benzimidazo-5-yl and/or benzimidazo[1,2-a]benzimidazo-2,5- ylene groups and in that at least one of the substituents B1, B2, B3, B4, B5, B6, B7 and B8 represents N; a process for their production and their use in electronic devices, especially electroluminescent devices. When used as host material for phosphorescent emitters in electroluminescent devices, the compounds of formula (I) may provide improved efficiency, stability, manufacturability, or spectral characteristics of electroluminescent devices.
    本发明涉及式(I)的化合物,其特征在于它们被苯并咪唑[1,2-a]苯并咪唑-5-基和/或苯并咪唑[1,2-a]苯并咪唑-2,5-基取代,并且至少一个取代基B1、B2、B3、B4、B5、B6、B7和B8代表N;一种生产它们的方法以及它们在电子器件中的应用,特别是电致发光器件。当作为电致发光器件中荧光发射剂的主体材料时,式(I)的化合物可能提供电致发光器件的效率、稳定性、可制造性或光谱特性的改进。
  • [EN] BENZIMIDAZOLO[2,1-B][1,3]BENZOTHIAZOLES FOR ELECTRONIC APPLICATIONS<br/>[FR] BENZIMIDAZOLO[2,1-B][1,3]BENZOTHIAZOLES POUR DES APPLICATIONS ÉLECTRONIQUES
    申请人:BASF SE
    公开号:WO2015014791A1
    公开(公告)日:2015-02-05
    The present invention relates to compounds of formula (I), a process for their production and their use in electronic devices, especially electroluminescent devices. When used as charge transport material and/or host material for phosphorescent emitters in electroluminescent devices, the compounds of formula (I) may provide improved efficiency, stability, manufacturability and/or spectral characteristics of electroluminescent devices.
    本发明涉及式(I)的化合物,其制备方法以及它们在电子器件中的应用,特别是电致发光器件。当作为电荷传输材料和/或荧光发射体在电致发光器件中的主体材料时,式(I)的化合物可能提供电致发光器件的效率、稳定性、可制造性和/或光谱特性的改进。
  • [EN] INDOLE DERIVATIVES FOR ELECTRONIC APPLICATIONS<br/>[FR] DÉRIVÉS D'INDOLE POUR DES APPLICATIONS ÉLECTRONIQUES
    申请人:IDEMITSU KOSAN CO
    公开号:WO2016079667A1
    公开(公告)日:2016-05-26
    The present invention relates to compounds of formula (I), a process for their production and their use in electronic devices, especially electroluminescent devices. When used as charge transport material and/or host material for phosphorescent emitters in electroluminescent devices, the compounds of formula I may provide improved efficiency and reduced driving voltage of electro- luminescent devices.
    本发明涉及公式(I)的化合物,其制备过程以及其在电子设备中的应用,特别是在电致发光设备中作为电荷传输材料和/或荧光发射体的载体材料时,公式I的化合物可以提供电致发光设备的改进效率和降低驱动电压。
  • [EN] 2,9-FUNCTIONALIZED BENZIMIDAZOLO[1,2-A]BENZIMIDAZOLES AS HOSTS FOR ORGANIC LIGHT EMITTING DIODES (OLEDS)<br/>[FR] BENZIMIDAZOLO[1,2-A] BENZIMIDAZOLES 2,9-FONCTIONNALISÉ UTILISÉS COMME HÔTES POUR DIODES ÉLECTROLUMINESCENTES ORGANIQUES (OLED)
    申请人:IDEMITSU KOSAN CO LTD IKC
    公开号:WO2016016791A1
    公开(公告)日:2016-02-04
    The present invention relates to compounds of formula (I), a process for their production and their use in electronic devices, especially electroluminescent devices. When used as charge transport material and/or host material for phosphorescent emitters in electroluminescent devices, the compounds of formula (I) may provide improved efficiency and reduced driving voltage of electroluminescent devices.
    本发明涉及式(I)化合物、其生产过程以及它们在电子器件中的使用,特别是在电致发光器件中。当作为电荷传输材料和/或电致发光器件中的荧光材料时,式(I)化合物可能提供电致发光器件的改进效率和降低驱动电压。
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同类化合物

迫萘合環己-1,3-二酮 赫金青霉素 萘嵌苯酮 富拉烯酮 9-羟基-萘嵌苯-1-酮 9-甲基氨基-萘嵌苯-1-酮 9-巯基-萘嵌苯-1-酮 9-去甲基FR-901235 9-二甲基氨基-1H-萘嵌苯-1-酮 9-丁氧基-1H-萘嵌苯-1-酮 6b,7a-二氢-7H-环丙并[a]苊烯-7-胺盐酸盐(1:1) 6-羟基-3-甲基-1H-萘嵌苯-1-酮 6-羟基-1H-萘嵌苯-1-酮 6-溴-1H-萉 6-氨基-1-萉酮 3-羟基-1H-PHENALEN-1-酮 2-甲氧基非那烯酮 2-甲基-1-氧代-1H-非那烯-3-乙酸 2-氯-6-(3-羟基丙基)氨基-1H-萉-1-酮 2,3-二氢-6-甲氧基萘嵌苯-1-酮 2,3-二氢-1H-萉 2,3-二氢-1H-苯并-1-酮 1H-非那烯并[2,1-d][1,3]噻唑 1H-非那烯 1H-萘嵌苯-1-酮腙 1-硫酮-9-甲基氨基-非那烯 (R)-8,9-二氢-4,5,6,7-四羟基-1,8,8,9-四甲基-3H-非那烯并(1,2-b)呋喃-3-酮 2-hydroxy-2-piperidino-phenalene-1,3-dione 9-[(4-pyrimidin-2-yl)piperazin-1-yl]-1H-phenalen-1-one N-[2-(4,9-dimethoxy-2,3-dihydro-1H-1-phenalenyl)ethyl]butanamide N-[2-(9-methoxy-2,3-dihydro-1H-1-phenalenyl)ethyl]butanamide 9-methyl-9-(2-methylpropenyl)-8,9-dihydrophenaleno[1,2-b]furan-7-one 3-((cyclohexylmethyl)amino)-6-(cyclohexylthio)-1-oxo-1H-phenalene-2-carbonitrile 9-(4-benzylpiperazin-1-yl)-1H-phenalen-1-one perchlorophenalenyl radical 6-((4-bromophenyl)thio)-1-oxo-1H-phenalene-2,3-dicarbonitrile methyl 3-((6-((4-bromophenyl)thio)-2-cyano-1-oxo-1H-phenalen-3-yl)amino)propanoate 3-((6-((4-bromophenyl)thio)-2-cyano-1-oxo-1H-phenalen-3-yl)amino)propanoic acid 3-((6-((4-bromophenyl)thio)-2-cyano-1-oxo-1H-phenalen-3-yl)amino)-N-(2-(2-hydroxyethoxy)ethyl)propanamide 1,1-dimethyl-1a,11b-dihydro-1H-benzo[k]cyclopropa[4,5]cyclopent[1,2,3-cd]fluoranthene 6-(cyclopentylthio)-1-oxo-1H-phenalene-2,3-dicarbonitrile 5-propyl-9-hydroxyphenalenone N-[2-(4,9-dimethoxy-2,3-dihydro-1H-1-phenalenyl)ethyl]propanamide N-[2-(4-methoxy-2,3-dihydro-1H-1-phenalenyl)ethyl]propanamide N-benzyl-1,2,3,10-tetrahydronaphtho[1,8-fg]indol-7-yl trifluoromethanesulfonate N-benzyl-7-ethyl-1,2,3,10-tetrahydronaphtho[1,8-fg]indole 1-oxo-1H-phenalene-2,3-dicarbonitrile 1-((1-oxo-1H-phenalen-2-yl)methyl)pyridinium chloride 9-[(2-hydroxyethyl)(methyl)amino]-1H-phenalen-1-one 6-phenylsulfanyl-2,3-dicyanophenalenone