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5-[4-(2,6-Diphenylpyrimidin-4-yl)phenyl]-12,12-dimethylindeno[1,2-c]carbazole

中文名称
——
中文别名
——
英文名称
5-[4-(2,6-Diphenylpyrimidin-4-yl)phenyl]-12,12-dimethylindeno[1,2-c]carbazole
英文别名
5-[4-(2,6-diphenylpyrimidin-4-yl)phenyl]-12,12-dimethylindeno[1,2-c]carbazole
5-[4-(2,6-Diphenylpyrimidin-4-yl)phenyl]-12,12-dimethylindeno[1,2-c]carbazole化学式
CAS
——
化学式
C43H31N3
mdl
——
分子量
589.739
InChiKey
YQCDYAINOBANTM-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):
    10.8
  • 重原子数:
    46
  • 可旋转键数:
    4
  • 环数:
    9.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    30.7
  • 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

  • 作为产物:
    描述:
    5,12-二氢-12,12-二甲基茚并[1,2-c]咔唑4-(4-溴苯基)-2,6-二苯基嘧啶tris-(dibenzylideneacetone)dipalladium(0)三叔丁基膦sodium t-butanolate 作用下, 以 甲苯 为溶剂, 反应 24.0h, 以64.3%的产率得到5-[4-(2,6-Diphenylpyrimidin-4-yl)phenyl]-12,12-dimethylindeno[1,2-c]carbazole
    参考文献:
    名称:
    一种以氮杂苯为核心的有机化合物及其应用
    摘要:
    本发明公开了一种以氮杂苯为核心的有机化合物及其应用,所述化合物中氮杂苯为A(acceptor,)基团、二苯并五元杂环衍生物为D(donor)基团,形成D‑A或D-π-A结构。本发明化合物具有分子间不易结晶、不易聚集、具有良好成膜性的特点,本发明化合物分子中的刚性基团可以提高材料的热稳定性,本发明化合物作为发光层材料应用于OLED,制作出的OLED器件具有良好的光电性能,能够更好的满足面板制造企业的要求。
    公开号:
    CN107586299A
点击查看最新优质反应信息

文献信息

  • Organic light-emitting device
    申请人:SAMSUNG DISPLAY CO., LTD.
    公开号:US10020459B2
    公开(公告)日:2018-07-10
    An organic light-emitting device includes: a first electrode, a second electrode facing the first electrode, and an organic layer between the first electrode and the second electrode, the organic layer including: an emission layer, an electron transport region between the second electrode and the emission layer, and a mixed layer between the emission layer and the electron transport region, the mixed layer including a first material and a second material, the first material and the second material being selected from a pyrrolidine-based compound and a C10-C30 polycyclicaromatic hydrocarbon-based compound, and a triplet energy EgT1 of at least one selected from the first material and the second material being 2.2 eV or greater.
    一种有机发光器件包括:第一电极、面向第一电极的第二电极以及位于第一电极和第二电极之间的有机层,有机层包括:发射层、位于第二电极和发射层之间的电子传输区域以及位于发射层和电子传输区域之间的混合层:发射层,第二电极和发射层之间的电子传输区,以及发射层和电子传输区之间的混合层,混合层包括第一材料和第二材料,第一材料和第二材料选自吡咯烷基化合物和 C10-C30 多环芳烃基化合物,以及选自第一材料和第二材料的至少一种材料的三重能 EgT1 为 2.2 eV 或更高。
  • ORGANIC ELECTROLUMINESCENCE DEVICE
    申请人:IDEMITSU KOSAN CO., LTD.
    公开号:US20140084270A1
    公开(公告)日:2014-03-27
    An organic electroluminescence device includes an anode, a cathode, a first organic layer and an emitting layer including a luminescent material, in which the first organic layer and the emitting layer are interposed between the anode and the cathode in this sequence from the anode. The emitting layer contains a first material represented by the following formula (1-1) and a second material. The first organic layer contains a compound represented by the following formula (4).
  • ORGANIC LIGHT-EMITTING DEVICE
    申请人:SAMSUNG DISPLAY CO., LTD.
    公开号:US20150325801A1
    公开(公告)日:2015-11-12
    An organic light-emitting device includes: a first electrode, a second electrode facing the first electrode, and an organic layer between the first electrode and the second electrode, the organic layer including: an emission layer, an electron transport region between the second electrode and the emission layer, and a mixed layer between the emission layer and the electron transport region, the mixed layer including a first material and a second material, the first material and the second material being selected from a pyrrolidine-based compound and a C 10 -C 30 polycyclicaromatic hydrocarbon-based compound, and a triplet energy Eg T1 of at least one selected from the first material and the second material being 2.2 eV or greater.
  • ORGANIC LIGHT-EMITTING DEVICE AND DISPLAY APPARATUS INCLUDING THE SAME
    申请人:Samsung Display Co., Ltd.
    公开号:US20200203621A1
    公开(公告)日:2020-06-25
    An organic light-emitting device includes a first electrode; a second electrode; and an organic layer between the first electrode and the second electrode. The organic layer includes an emission layer. The emission layer includes a first compound, a second compound, and a third compound. The first compound is represented by Formula 1, the second compound is represented by Formula 2, the third compound is represented by Formula 3, and the first compound and the second compound are different from each other.
  • LIGHT-EMITTING ELEMENT MATERIAL CONTAINING PYRROMETHENE BORON COMPLEX, LIGHT-EMITTING ELEMENT, DISPLAY DEVICE, AND ILLUMINATION DEVICE
    申请人:Toray Industries, Inc.
    公开号:US20220407007A1
    公开(公告)日:2022-12-22
    The present invention provides a pyrromethene boron complex represented by the general formula (1), a light emitting element material having high luminance efficiency, and a light emitting element: wherein X 1 and X 2 each may be the same or different, and are selected from the group consisting of an alkyl group, a cycloalkyl group, a heterocyclic group, an alkenyl group, a cycloalkenyl group, an alkynyl group, a hydroxyl group, a thiol group, an alkoxy group, a cycloalkoxy group, an alkylthio group, an aryl ether group, an aryl thioether group, an aryl group, a heteroaryl group, halogen and a cyano group. These functional groups may further have a substituent. Ar 1 to Ar 4 each may be the same or different, and are a substituted or unsubstituted aryl group, or a substituted or unsubstituted heteroaryl group. The aryl group and the heteroaryl group may be either a monocyclic ring or a fused ring. However, when one or both of Ar 1 and Ar 2 is/are monocyclic ring(s), the monocyclic ring has one or more secondary alkyl groups, one or more tertiary alkyl groups, one or more aryl groups, or one or more heteroaryl groups as substituents, or has a methyl group and a primary alkyl group as two or more substituents in total. R 1 and R 2 each may be the same or different, and are a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heteroaryl group. R 3 to R 5 each may be the same or different, and are selected from the group consisting of a hydrogen atom, an alkyl group, a cycloalkyl group, a heterocyclic group, an alkenyl group, a cycloalkenyl group, an alkynyl group, an aryl group, a heteroaryl group, a hydroxyl group, a thiol group, an alkoxy group, an alkylthio group, an aryl ether group, an aryl thioether group, halogen, a cyano group, an aldehyde group, an acyl group, a carboxyl group, an ester group, an amide group, a sulfonyl group, a sulfonic acid ester group, a sulfonamide group, an amino group, a nitro group, a silyl group, and a ring structure with an adjacent group. These functional groups may further have a substituent. R 6 and R 7 each may be the same or different, and are selected from the group consisting of a hydrogen atom, an alkyl group, a cycloalkyl group, a heterocyclic group, an alkenyl group, a cycloalkenyl group, an alkynyl group, an aryl group, a heteroaryl group, a hydroxyl group, a thiol group, an alkoxy group, an alkylthio group, an aryl ether group, an aryl thioether group, halogen, a cyano group, an aldehyde group, an acyl group, a carboxyl group, an ester group, an amide group, a sulfonyl group, a sulfonic acid ester group, a sulfonamide group, an amino group, a nitro group and a silyl group. However, R 6 may be a bridging structure formed by covalent bond via one or two atoms with Ar 4 , and R 7 may be a bridging structure formed by covalent bond via one or two atoms with Ar 3 . These functional groups may further have a substituent.
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