WO2016141691A1 - 有机电子材料 - Google Patents

有机电子材料 Download PDF

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WO2016141691A1
WO2016141691A1 PCT/CN2015/088709 CN2015088709W WO2016141691A1 WO 2016141691 A1 WO2016141691 A1 WO 2016141691A1 CN 2015088709 W CN2015088709 W CN 2015088709W WO 2016141691 A1 WO2016141691 A1 WO 2016141691A1
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substituted
group
unsubstituted
alkyl
phenyl
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PCT/CN2015/088709
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English (en)
French (fr)
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鲁锦鸿
李哲
陈金鑫
蔡丽菲
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广东阿格蕾雅光电材料有限公司
北京阿格蕾雅科技发展有限公司
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Application filed by 广东阿格蕾雅光电材料有限公司, 北京阿格蕾雅科技发展有限公司 filed Critical 广东阿格蕾雅光电材料有限公司
Priority to DE112015006276.9T priority Critical patent/DE112015006276B4/de
Priority to US15/557,097 priority patent/US10347843B2/en
Priority to KR1020177025531A priority patent/KR101992318B1/ko
Priority to JP2017547496A priority patent/JP6516861B2/ja
Publication of WO2016141691A1 publication Critical patent/WO2016141691A1/zh

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    • C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
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Definitions

  • the invention relates to a novel organic electroluminescent material, which is deposited into a thin film by vacuum evaporation, and is applied as a blue electroluminescent material on an organic electroluminescent diode, and belongs to the technical field of organic electroluminescent device display.
  • organic electroluminescent devices As a new display technology, organic electroluminescent devices have self-luminous, wide viewing angle, low power consumption, high efficiency, thin, rich color, fast response, wide temperature range, low driving voltage, flexible and bendable Transparent display panels and environmentally friendly features, therefore, organic electroluminescent device technology can be applied to flat panel displays and next-generation lighting, as well as backlights for LCDs.
  • An organic electroluminescent device is a device prepared by spin coating or depositing an organic material between two metal electrodes.
  • a classic three-layer organic electroluminescent device comprises a hole transport layer, a light emitting layer and an electron transport layer. The holes generated by the anode pass through the hole transport layer and the electrons generated by the cathode are combined by the electron transport layer to form excitons in the light-emitting layer, and then emit light.
  • the organic electroluminescent device can emit red light, green light, and blue light by changing the material of the light emitting layer. Therefore, stable, high-efficiency and color-purity organic electroluminescent materials play an important role in the application and promotion of organic electroluminescent devices, and are also an urgent need for the application of OLEDs for large-area panel displays.
  • red and green materials have recently achieved great development and are also in line with the market demand for panels.
  • blue light materials there are also a series of commercial materials, among which the distyrylbiphenyl (DPVBi) compounds of Idemitsu Kosan Co., Ltd., which were used in the early days, were prepared from such compounds.
  • the devices have higher efficiency, but often the stability of these materials is relatively poor.
  • the luminescent color of such compounds belongs to sky blue, and y>0.15 in the CIE value. Therefore, due to its poor temperature and impure color, the application of such compounds in full color display devices is greatly limited.
  • Another type of blue light material is Kodak's ADN and tetra-tert-butyl fluorene, but these compounds have relatively poor luminous efficiency and poor stability, so they cannot be used in large quantities.
  • the invention overcomes the defects of the above compounds and provides a series of organic electroluminescent materials having good thermal stability, high luminous efficiency and high luminous purity, and the organic electroluminescent device prepared therefrom has good electroluminescence efficiency and color. Excellent in purity and long life.
  • the organic electronic material of the present invention has the structural formula of the formula (I):
  • R 1 - R 17 are independently represented by hydrogen, deuterium, halogen, cyano, nitro, C1-C8 alkyl, C1-C8 alkoxy, C6-C30 substituted or unsubstituted aryl, C3 a substituted or unsubstituted heteroaryl aryl group of C30, a C2-C8 substituted or unsubstituted olefinic group, a C2-C8 substituted or unsubstituted alkynyl group, wherein Ar 1 -Ar 3 A C6-C60 substituted or unsubstituted aryl group, a C3-C60 substituted or unsubstituted heteroaryl group having one or more hetero atoms, a triaromatic (C6-C30) amine group.
  • R 1 - R 17 are independently represented by hydrogen, halogen, cyano, nitro, C1-C8 alkyl, C1-C8 alkoxy, C2-C8 substituted or unsubstituted olefinic alkyl, C2- a C8 substituted or unsubstituted alkynyl group, a C1-C4 alkyl substituted or unsubstituted phenyl group, a C1-C4 alkyl substituted or unsubstituted naphthyl group, or a C1-C4 alkyl group substituted or unsubstituted fluorene
  • Ar 1 -Ar 3 independently represents a C1-C4 alkyl group or a C6-C30 aryl-substituted phenyl group, a C1-C4 alkyl group or a C6-C30 aryl-substituted naphthyl group, a phenyl group, a
  • R 1 -R 2 may independently be preferably represented by hydrogen, halogen, C1-C4 alkyl, C1-C4 alkyl substituted or unsubstituted phenyl, C1-C4 alkyl substituted or unsubstituted naphthalene Or a C1-C4 alkyl-substituted or unsubstituted fluorenyl group; wherein R 3 - R 17 may independently be preferably represented by hydrogen, halogen, C1-C4 alkyl, C1-C4 alkyl substituted or not Substituted phenyl, C1-C4 alkyl substituted or unsubstituted naphthyl, preferably Ar 1 -Ar 3 independently represents phenyl, tolyl, xylyl, tert-butylphenyl, naphthyl, pyridyl, Methylnaphthalene, biphenyl, diphenylphen
  • R 3 - R 17 are preferably hydrogen
  • R 1 , R 2 may independently and preferably represent hydrogen, methyl, ethyl, propyl, isopropyl, t-butyl, phenyl, biphenyl, naphthalene.
  • Ar 1 -Ar 3 independently represents phenyl, pyridyl, tolyl, xylyl, naphthyl, methylnaphthalene, biphenyl, diphenylphenyl, naphthylbenzene Base, diphenylbiphenyl, (9,9-dialkyl)fluorenyl, (9,9-dimethyl substituted or unsubstituted phenyl) anthracenyl, 9,9-spiropurinyl.
  • R 3 - R 17 are preferably hydrogen; R 1 , R 2 independently represent hydrogen, methyl, or a fluorenyl group; and Ar 1 , Ar 2 , and Ar 3 independently represent a phenyl group, a naphthyl group.
  • organic electronic materials are used in the field of organic electroluminescent devices, organic solar cells, organic thin film transistors or organic photoreceptors.
  • the organic electronic material provided by the present invention can be fabricated into an organic electroluminescent device comprising an anode, a cathode and one or more organic layers, at least one of which contains an organic electronic material as described in Structural Formula I.
  • the plurality of organic layers are respectively a hole injection layer, a hole transport layer, a light-emitting layer, an electron transport layer or/and an electron injection layer, and it is particularly noted that the organic layer may not necessarily exist in each layer as needed. .
  • the hole transport layer, the electron transport layer, and the light-emitting layer contain the organic material as described in Structural Formula 1.
  • the hole transport layer and the hole injection layer in the present invention have a good hole transporting property and are capable of efficiently transporting holes from the anode to the organic light-emitting layer. It may include small molecules and high molecular organic materials, and may include, but is not limited to, triarylamine compounds, biphenyldiamine compounds, thiazole compounds, oxazole compounds, imidazole compounds, terpenoids, phthalocyanine compounds, Hexanitrile hexaazatriphenylene, 2,3,5,6-tetrafluoro-7,7',8,8'-tetracyanodimethyl-p-benzoquinone (F4-TCNQ), polyvinyl Carbazole, polythiophene, polyethylene, polybenzenesulfonic acid.
  • the organic electroluminescent layer of the present invention may contain, in addition to the compound of the structural formula (I) of the present invention, the following compounds, but is not limited thereto, naphthalene compounds, terpenoids, terpenoids, phenanthrene compounds, and quinones. Compounds, fluoranthene compounds, terpenoids, pentacene compounds, terpenoids, diarylene compounds, triphenylamine vinyl compounds, amine compounds, benzimidazoles, furan compounds, organic metal chelate Compound.
  • the organic electron transporting material used in the organic electronic device of the present invention is required to have good electron transporting property, and can efficiently transport electrons from the cathode to the light emitting layer, and the following compounds can be selected, but are not limited thereto, oxazole, thiazole Compounds, triazoles, triazazines, triazabenzenes, porphyrins, diazonium compounds, silicon-containing heterocyclic compounds, quinoline compounds, phenanthroline compounds , metal chelate, fluorine-substituted benzene compound.
  • the organic electronic device of the present invention may be provided with an electron injecting layer which can efficiently inject electrons from the cathode into the organic layer, mainly selected from alkali metal or alkali metal compounds, or selected from alkaline earth metals.
  • an alkaline earth metal compound the following compounds may be selected, but are not limited thereto, lithium, lithium fluoride, lithium oxide, lithium nitride, lithium quinolate, hydrazine, cesium carbonate, 8-hydroxyquinolinium, calcium, Calcium fluoride, calcium oxide, magnesium, magnesium fluoride, magnesium carbonate, magnesium oxide.
  • the device experiments show that the organic electronic material of the invention according to formula (I) has good thermal stability, high luminous efficiency and high luminous purity.
  • the organic electroluminescent device fabricated using the organic light-emitting material has the advantages of good electroluminescence efficiency, excellent color purity, and long life.
  • Figure 1 is a structural view of a device of the present invention
  • 10 represents a glass substrate
  • 20 represents an anode
  • 30 represents a hole injection layer
  • 40 represents a hole transport layer
  • 50 represents a light-emitting layer
  • 60 represents an electron transport layer
  • 70 represents an electron injection layer
  • 80 represents an electron injection layer. It is a cathode.
  • Figure 3 is a 13 C NMR chart of Compound 89.
  • Figure 5 is a TGA diagram of Compound 89.
  • Example 6 is a graph showing voltage-current density of Example 4, Example 5, and Comparative Example 1.
  • Example 7 is a graph of brightness-CIEy of Example 4, Example 5 and Comparative Example 1.
  • Example 8 is an electroluminescence spectrum of Example 4, Example 5 and Comparative Example 1.
  • Example 9 is a graph showing current density-current efficiency of Example 4, Example 5 and Comparative Example 1.
  • the transparent conductive ITO glass substrate 10 (with the anode 20 on the surface) was sequentially washed with a detergent solution and deionized water, ethanol, acetone, deionized water, and then treated with oxygen plasma for 30 seconds.
  • NPB was evaporated to form a hole transport layer 40 having a thickness of 30 nm.
  • a compound 3 having a thickness of 30 nm was vapor-deposited on the hole transport layer as the light-emitting layer 50.
  • the prepared device had a voltage of 3.58 V at an operating current density of 20 mA/cm 2 , a current efficiency of 3.21 cd/A, and a CIEy coordinate of 0.0853 at a luminance of 1000 cd/m 2 to emit blue light.
  • the prepared device had a voltage of 3.84 V at an operating current density of 20 mA/cm 2 , a current efficiency of 2.83 cd/A, a CIEy coordinate of 0.0888 at a luminance of 1000 cd/m 2 , and emission of blue light.
  • the prepared device had a voltage of 4.00 V at an operating current density of 20 mA/cm 2 , a current efficiency of 2.46 cd/A, a CIEy coordinate of 0.0952 at a luminance of 1000 cd/m 2 , and emission of blue light.
  • Examples 4 and 5 are specific applications of the materials of the present invention.
  • the devices produced, which emit blue light, have higher efficiency and brightness than the comparative examples.
  • the material of the present invention has high stability, and the organic electroluminescent device prepared by the present invention has high efficiency and light purity.

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  • Engineering & Computer Science (AREA)
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  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Optics & Photonics (AREA)
  • Electroluminescent Light Sources (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Photovoltaic Devices (AREA)

Abstract

提供了式(I) 所示的有机电子材料，属于有机电致发光器件显示材料技术领域。该有机电子材料具有较好热稳定性，高发光效率，高发光纯度。采用该有机发光材料制作的有机电致发光器件具有电致发光效率良好和色纯度优异以及寿命长的优点。

Description

有机电子材料 技术领域
本发明涉及新型的有机电致发光材料，通过真空蒸渡沉积成薄膜，作为蓝光电致发光材料应用在有机电致发光二极管上，属于有机电致发光器件显示技术领域。
背景技术
有机电致发光器件作为一种新型的显示技术，具有自发光、宽视角、低能耗、效率高、薄、色彩丰富、响应速度快、适用温度范围广、低驱动电压、可制作柔性可弯曲与透明的显示面板以及环境友好等独特优点，因此，有机电致发光器件技术可以应用在平板显示器和新一代照明上，也可以作为LCD的背光源。
有机电子发光器件为在两个金属电极之间通过旋涂或者沉积一层有机材料而制备的器件，一个经典的三层有机电致发光器件包含空穴传输层，发光层和电子传输层。由阳极产生的空穴经空穴传输层跟由阴极产生的电子经电子传输层结合在发光层形成激子，而后发光。有机电致发光器件可以通过改变发光层的材料来发射红光，绿光和蓝光。因而，稳定的，高效的和色彩纯的有机电致发光材料对有机电致发光器件的应用和推广具有重要作用，同时也是OLEDs大面积面板显示的应用推广的迫切需求。
在三原色(红，蓝，绿)当中，红光和绿光材料最近已经取得了很大的发展，也符合面板的市场需求。对于蓝光材料，也有一系列的商品化的材料，其中早期用得比较多的为出光兴产(Idemitsu Kosan Co.,Ltd)的二苯乙烯基联苯(DPVBi)类化合物，以这类化合物制备的器件具有较高的效率，但是往往这些材料的稳定性比较差，更有甚地，这类化合物的发光的颜色属于天蓝光，往往CIE值中的y>0.15。所以由于其不好的温度性和不纯的颜色很大程度地限制了这类化合物在全彩显示器件中的应用。另外一类蓝光材料为柯达公司的ADN和四叔丁基苝，但是这些化合物的发光效率比较差，而且稳定性也不好，从而无法大量使用。
Figure PCTCN2015088709-appb-000001
发明内容
本发明就是克服上面化合物的缺陷，提供一系列具有较好热稳定性，高发光效率，高发光纯度的有机电致蓝光材料，由它制备的有机电致发光器件具有电致发光效率良好和色纯度优异以及寿命长的优点。
本发明所述的有机电子材料具有式(I)所述的结构式：
Figure PCTCN2015088709-appb-000002
其中，R1-R17独立地表示为氢，氘原子，卤素，氰基，硝基，C1-C8烷基、C1-C8烷氧基，C6-C30的取代或者未取代的芳基，C3-C30的取代或者未取代的含有一个或者多个的杂原子芳基，C2-C8取代或者未取代的烯烷基，C2-C8取代或者未取代的炔烷基，其中，Ar1-Ar3独立地表示C6-C60取代或者未取代的芳基，C3-C60的取代或者未取代的带有一个或者多个杂原子的杂芳基，三芳香(C6-C30)胺基。
优选：其中，R1-R17独立地表示为氢，卤素，氰基，硝基，C1-C8烷基、C1-C8烷氧基，C2-C8取代或者未取代的烯烷基，C2-C8取代或者未取代的炔烷基，C1-C4烷基取代或未取代的苯基，C1-C4烷基取代或未取代的萘基，或结合成C1-C4烷基取代或未取代的芴基；Ar1-Ar3独立地表示C1-C4烷基或者C6-C30芳基取代的苯基，C1-C4烷基或者C6-C30芳基取代的萘基，苯基，萘基，吡啶基，N-C6-C30的芳基或者C1-C4的烷基取代的咔唑基，二苯并噻吩基，二苯并呋喃基，蒽基，菲基，芘基，苝基，荧蒽基，(9,9-二烷基)芴基，(9,9-二烷基取代或未取代芳基)芴基，9,9-螺芴基。
优选：其中，R1-R2可以独立地优选表示为氢，卤素，C1-C4的烷基，C1-C4烷基取代或未取代的苯基，C1-C4烷基取代或未取代的萘基，或结合成C1-C4烷基取代或未取代的芴基；其中，R3-R17可以独立地优选表示为氢，卤素，C1-C4的烷基，C1-C4烷基取代或未取代的苯基，C1-C4烷基取代或未取代的萘基，优选Ar1-Ar3为独立地表示苯基，甲苯基，二甲 苯基，叔丁基苯基，萘基，吡啶基，甲基萘，联苯基，二苯基苯基，萘基苯基，二苯基联苯基，二芳香胺基苯基，N-苯基咔唑基，(9,9-二烷基)芴基，(9,9-二烷基取代或未取代苯基)芴基，9,9-螺芴基。
优选：其中，R3-R17优选为氢，R1，R2可以独立优选表示为氢，甲基，乙基，丙基，异丙基，叔丁基，苯基，联苯基，萘基，或结合成芴基；Ar1-Ar3为独立地表示苯基，吡啶基，甲苯基，二甲苯基，萘基，甲基萘，联苯基，二苯基苯基，萘基苯基，二苯基联苯基，(9,9-二烷基)芴基，(9,9-二甲基取代或未取代苯基)芴基，9,9-螺芴基。
优选：R3-R17优选为氢；R1，R2为独立地表示氢，甲基，或结合成芴基；Ar1，Ar2，Ar3为独立地表示苯基，萘基。
优选：
Figure PCTCN2015088709-appb-000003
上述有机电子材料在有机电致发光器件，有机太阳能电池，有机薄膜晶体管或有机光感受器领域的应用。
如上面提到的，本发明的具体实施例如下，但不限于所列举的结构：
Figure PCTCN2015088709-appb-000004
Figure PCTCN2015088709-appb-000005
Figure PCTCN2015088709-appb-000006
Figure PCTCN2015088709-appb-000007
Figure PCTCN2015088709-appb-000008
Figure PCTCN2015088709-appb-000009
Figure PCTCN2015088709-appb-000010
Figure PCTCN2015088709-appb-000011
Figure PCTCN2015088709-appb-000012
Figure PCTCN2015088709-appb-000013
Figure PCTCN2015088709-appb-000014
Figure PCTCN2015088709-appb-000015
Figure PCTCN2015088709-appb-000016
Figure PCTCN2015088709-appb-000017
Figure PCTCN2015088709-appb-000018
Figure PCTCN2015088709-appb-000019
Figure PCTCN2015088709-appb-000020
Figure PCTCN2015088709-appb-000021
Figure PCTCN2015088709-appb-000022
Figure PCTCN2015088709-appb-000023
Figure PCTCN2015088709-appb-000024
Figure PCTCN2015088709-appb-000025
Figure PCTCN2015088709-appb-000026
Figure PCTCN2015088709-appb-000027
Figure PCTCN2015088709-appb-000028
Figure PCTCN2015088709-appb-000029
本发明提供的有机电子材料可以制成有机电致发光器件，该器件包含阳极，阴极和一层或多层有机层，所述有机层中至少有一层含有如结构式I所述的有机电子材料。
所述多层有机层分别为空穴注入层，空穴传输层，发光层，电子传输层或/和电子注入层，需要特别指出，上述有机层可以根据需要，这些有机层不必每层都存在。
所述空穴传输层，电子传输层和发光层中含有如结构式1所述的有机材料。
本发明中的空穴传输层和空穴注入层，所需材料具有很好的空穴传输性能，能够有效地把空穴从阳极传输到有机发光层上。可以包括小分子和高分子有机材料，可以包含如下，但是不限于这些，三芳香胺化合物，联苯二胺化合物，噻唑化合物，恶唑化合物，咪唑类化合物，芴类化合物，酞菁类化合物，六氰基六杂三苯(hexanitrile hexaazatriphenylene)，2,3,5,6-四氟-7,7',8,8'-四氰二甲基对苯醌(F4-TCNQ)，聚乙烯基咔唑，聚噻吩，聚乙烯，聚苯磺酸。
本发明的有机电致发光层，除含有本发明的结构式(I)化合物外，还可以含有如下化合物，但是不限于此，萘类化合物，芘类化合物，芴类化合物，菲类化合物，屈类化合物，荧蒽类化合物，蒽类化合物，并五苯类化合物，苝类化合物，二芳乙烯类化合物，三苯胺乙烯类化合物，胺类化合物，苯并咪唑类化合物，呋喃类化合物，有机金属螯合物。
本发明的有机电子器件使用的有机电子传输材料要求具有很好的电子传输性能，能够有效地把电子从阴极传输到发光层中，可以选择如下化合物，但是不限于此，氧杂恶唑，噻唑类化合物，三氮唑类化合物，三氮嗪类化合物，三氮杂苯类化合物，喔啉类化合物，二氮蒽类化合物，含硅杂环类化合物，喹啉类化合物，菲啰啉类化合物，金属螯合物，氟取代苯类化合物。
本发明的有机电子器件根据需要，可以加入一层电子注入层，该电子注入层可以有效的把电子从阴极注入到有机层中，主要选自碱金属或者碱金属的化合物，或选自碱土金属或者碱土金属的化合物，可以选择如下化合物，但是不限于此，锂，氟化锂，氧化锂，氮化锂，8-羟基喹啉锂，铯，碳酸铯，8-羟基喹啉铯，钙，氟化钙，氧化钙，镁，氟化镁，碳酸镁，氧化镁。
器件实验表明，本发明如式(I)所述的有机电子材料，具有较好热稳定性，高发光效率，高发光纯度。采用该有机发光材料制作的有机电致发光器件具有电致发光效率良好和色纯度优异以及寿命长的优点。
附图说明
图1为本发明的器件结构图，
其中10代表为玻璃基板，20代表为阳极，30代表为空穴注入层，40代表为空穴传输层，50代表为发光层，60代表为电子传输层，70代表为电子注入层，80代表为阴极。
图2为化合物89的1H NMR图。
图3为化合物89的13C NMR图。
图4为化合物89的HPLC图。
图5为化合物89的TGA图。
图6为实施例4,实施例5及比较例1的电压–电流密度曲线图
图7为实施例4,实施例5及比较例1的亮度–CIEy坐标图
图8为实施例4,实施例5及比较例1的电致发光光谱
图9为实施例4,实施例5及比较例1的电流密度–电流效率曲线图
具体实施方式
为了更详细叙述本发明，特举以下例子，但是不限于此。
(其中下面的化合物1a、1b、1e、1h，3a、89a为市售的常用材料)
实施例1
Figure PCTCN2015088709-appb-000030
中间体1c的合成
向反应烧瓶中加入1a(240.00g,0.88mol),1b(496.32g,1.76mol),Pd(PPh3)4(20.35g,17.60mmol)，碳酸钾(302.52g,2.20mol)，甲苯(2400mL)，纯水(1200mL)。抽放氮气三次后开启加热，待反应液温度达到95-105℃，保持此温度反应8-12h，取样TLC及HPLC，原料反应完全。停止加热，降温至20-30℃，抽滤，滤液分出有机层，水层再用乙酸乙酯萃取，合并有机层，再用水洗，无水硫酸镁干燥，抽滤，滤液浓缩得到暗黄色固体粗产品。石油醚重结晶，得到灰白色固体产品，收率90％，纯度95％。
中间体1d的合成
向反应烧瓶中加入相应比例的1c(302g,0.78mol),B(OEt)3(142g,0.97mol),n-BuLi/THF(1.6M,600mL),无水THF(3000mL)，抽放氮气三次后冷却降温至反应液温度至-75～-65℃，缓慢滴加n-BuLi/THF溶液，控制反应液温度在-75～-65℃，滴加完毕后，继续保持此温度反应0.5-1h。后将一定量的B(OEt)3滴加进去，控制反应液温度在-75～-65℃，滴加完毕后，继续保持此温度反应0.5-1h，后反应液移至室温自然升温反应4-6h，然后加入2M 稀盐酸，调节PH值至2-3，搅拌约1h，停止反应。加入乙酸乙酯萃取，水层再用EA萃取，合并有机层，无水硫酸镁干燥，抽滤，滤液浓缩得到得到灰白色固体产品，纯度95％，收率62.5％。
中间体1f的合成
向反应烧瓶中加入1d(150g,0.43mol),1e(500g,0.86mol),Pd(PPh3)4(5.0g,0.44mmol)，碳酸钾(130g,0.92mol)，甲苯(1000mL)，纯水(500mL),抽放氮气三次开启加热，待反应液温度达到95-105℃，保持此温度反应8-12h，取样TLC及HPLC，原料反应完全。停止加热，降温至20-30℃，抽滤，滤液分出有机层，水层再用乙酸乙酯萃取，合并有机层，无水硫酸镁干燥，抽滤，滤液浓缩得到暗黄色固体粗产品，纯度80％，收率78.1％。
中间体1g的合成
向反应烧瓶中加入1f(210g,0.42mol),NBS(135g,0.71mol),DMF(5L)。抽放氮气三次开启加热，待反应液温度达到60-65℃，保持此温度反应6-8h，取样TLC及HPLC，原料反应完全。停止加热，降温至20-30℃，反应液倒入冰水中，析出暗黄色固体，抽滤得到黄色固体，烘干得到1g粗产品。粗产品加入DCM/MeOH至溶液稍微变混浊，继续搅拌约30min，析出大量固体，抽滤，得到浅黄色固体产品，收率约54.05％，纯度98.5％
1H NMR(300MHz,CDCl3)δ8.64(d,J＝8.8Hz,2H),7.99–7.90(m,4H),7.87(t,J＝1.6Hz,1H),7.78(dd,J＝9.3,2.3Hz,6H),7.61(ddd,J＝8.8,6.5,1.1Hz,2H),7.56–7.48(m,6H),7.46–7.38(m,4H).
13C NMR(76MHz,CDCl3)δ142.67(s),142.03(s),141.26(s),140.69(s),137.83(s),137.52(s),131.87(s),131.24(s),130.44(s),129.09(s),128.80(s),128.38–127.40(m),127.18(s),126.05–125.21(m),123.08(s),77.74(s),77.31(s),76.89(s),30.10(s).
化合物1的合成
向500ml三口烧瓶中依次加入1g(9.5g,16.92mmol),1h(6.41g,30.51mmol),Pd(PPh3)4(1.5g,1.3mmol)，碳酸钾(5.84g,42.3mmol)，甲苯(150mL)，纯水(75mL)。抽放氮气三次后105℃下反应。由液相检测停反应时间，约12h左右。反应开始时反应液为催化剂的土黄色，之后慢慢变成黄色溶液，停反应后上层为清亮浅黄色，下层为水。停止反应后，过滤，用乙酸乙酯洗滤渣直至滤渣中无产物，收集滤液，旋干，大量的灰白色固体析出，收集 滤渣干燥，得到目标产物，纯度98％。真空升华得到纯度为99.5％灰白色固体粉末。
1H-NMR(300MHz,CDCl3)δ8.10–8.21(d，2H)，7.96–7.98(dd，3H)，7.87–7.89(m，2H)，7.81–7.86(m，4H)，7.78–7.81(d，4H),7.62–7.65(m，2H)，7.59(s，1H)，7.51–7.57(m，5H)，7.45–7.48(m，2H)，7.36–7.43(m，7H)，3.88(s，2H).
实施例2
化合物3的合成
Figure PCTCN2015088709-appb-000031
向500ml三口烧瓶中依次加入1g(9.5g,16.92mmol),3a(7.25g,30.46mmol),Pd(PPh3)4(1.5g,1.3mmol)，碳酸钾(5.84g,42.3mmol)，甲苯(150mL)，纯水(75mL)。抽放氮气三次后105℃下反应。由液相检测停反应时间，约12h左右。反应开始时反应液为催化剂的土黄色，之后慢慢变成黄色溶液，停反应后上层为清亮浅黄色，下层为水。停止反应后，过滤，用乙酸乙酯洗滤渣直至滤渣中无产物，收集滤液，旋干，大量的灰白色固体析出，收集滤渣干燥，得到目标产物，纯度98％。真空升华得到纯度为99.7％灰白色固体粉末。
1H-NMR(300MHz,CDCl3)δ8.1–8.2(d，2H)，7.96–7.99(dd，3H)，7.88–7.89(m，2H)，7.81–7.86(m，4H)，7.78–7.81(d，4H),7.61–7.65(m，2H)，7.59(s，1H)，7.51–7.56(m，5H)，7.46–7.48(m，2H)，7.35–7.43(m，7H)，1.61(s，6H).
实施例3
化合物89的合成
Figure PCTCN2015088709-appb-000032
向反应容器中依次加入1g(10.0g,17.8mmol),89a(7.1g,19.6mmol),Pd(PPh3)4(432.2mg,0.35mmol),K2CO3(6.14g,44.5mmol),甲苯(300mL)和水(150mL)，对装置进行除氧、通入氮气保护，然后加热到100℃反应过夜。用DCM：PE＝1:5的比例点板，产物点在365nm波长的紫外灯下发强烈的蓝光，Rf值在0.2左右。将反应液用硅胶抽滤，然后将滤饼用乙酸乙酯(100mL)洗涤两次，分液，用乙酸乙酯(100mL)萃取水层一次，合并有机层，再用水(200mL)洗涤一次有机相。旋干除去溶剂。粗品用120ml DCM/MeOH重结晶，抽滤得到黄色固体粉末13.1g，纯度为98.7％，收率92.2％。真空升华得到纯度为99.7％浅黄色固体粉末。m/z＝797.
从图2和图3可见化合物89的氢谱，碳谱与结构完全一致。从图4化合物89的高效液相色谱图可见根据本发明的合成方法制备的产物具有高纯度。从图5化合物89的热重分析图可见这类型化合物的分解温度高于摄氏400度，表明其非常高热稳定性。
实施例4
有机电致发光器件1的制备
使用本发明的有机电子材料制备OLED
首先，将透明导电ITO玻璃基板10(上面带有阳极20)依次经：洗涤剂溶液和去离子水，乙醇，丙酮，去离子水洗净，再用氧等离子处理30秒。
然后，在ITO上蒸渡10nm厚的HAT-CN6作为空穴注入层30。
然后，蒸渡NPB,形成30nm厚的空穴传输层40。
然后，在空穴传输层上蒸渡30nm厚的化合物3作为发光层50。
然后，在发光层上蒸渡15nm厚的TPBi作为电子传输层60。
最后，蒸渡15nm BPhen:Li为电子注入层70和150nm Al作为器件阴极80。
所制备的器件在20mA/cm2的工作电流密度下的电压为3.58V，电流效率达到3.21cd/A，在1000cd/m2亮度下CIEy坐标为0.0853，发射蓝光。
器件中所述结构式
Figure PCTCN2015088709-appb-000033
实施例5
有机电致发光器件2的制备
方法同实施例4,将化合物3，换成化合物89，制作有机电致发光器件。
所制备的器件在20mA/cm2的工作电流密度下的电压为3.84V,电流效率达到2.83cd/A，在1000cd/m2亮度下CIEy坐标为0.0888，发射蓝光。
比较例1
方法同实施例4，将化合物3替换成下列化合物TAT，制作对比用有机电致发光器件。
TAT结构式
Figure PCTCN2015088709-appb-000034
所制备的器件在20mA/cm2的工作电流密度下的电压为4.00V,电流效率达到2.46cd/A，在1000cd/m2亮度下CIEy坐标为0.0952，发射蓝光。
实施例4和5是本发明材料的具体应用，所制备的器件，本发明发射蓝光，效率和亮度都高于对比例。如上所述，本发明的材料具有高的稳定性，本发明制备的有机电致发光器件具有高的效率和光纯度。

Claims (8)

  1. 有机电子材料，具有式(I)所述的结构式：
    Figure PCTCN2015088709-appb-100001
    其中，R1-R17独立地表示为氢，氘原子，卤素，氰基，硝基，C1-C8烷基、C1-C8烷氧基，C6-C30的取代或者未取代的芳基，C3-C30的取代或者未取代的含有一个或者多个的杂原子芳基，C2-C8取代或者未取代的烯烷基，C2-C8取代或者未取代的炔烷基，其中，Ar1-Ar3独立地表示C6-C60取代或者未取代的芳基，C3-C60的取代或者未取代的带有一个或者多个杂原子的杂芳基，三芳香(C6-C30)胺基。
  2. 根据权利要求1所述的有机电子材料，其中，R1-R17独立地表示为氢，卤素，氰基，硝基，C1-C8烷基、C1-C8烷氧基，C2-C8取代或者未取代的烯烷基，C2-C8取代或者未取代的炔烷基，C1-C4烷基取代或未取代的苯基，C1-C4烷基取代或未取代的萘基，或结合成C1-C4烷基取代或未取代的芴基；Ar1-Ar3独立地表示C1-C4烷基或者C6-C30芳基取代的苯基，C1-C4烷基或者C6-C30芳基取代的萘基，苯基，萘基，吡啶基，N-C6-C30的芳基或者C1-C4的烷基取代的咔唑基，二苯并噻吩基，二苯并呋喃基，蒽基，菲基，芘基，苝基，荧蒽基，(9,9-二烷基)芴基，(9,9-二烷基取代或未取代芳基)芴基，9,9-螺芴基。
  3. 根根据权利要求2所述的有机电子材料，其中，R1-R2可以独立地优选表示为氢，卤素，C1-C4的烷基，C1-C4烷基取代或未取代的苯基，C1-C4烷基取代或未取代的萘基，或结合成C1-C4烷基取代或未取代的芴基；其中，R3-R17可以独立地优选表示为氢，卤素，C1-C4的烷基，C1-C4烷基取代或未取代的苯基，C1-C4烷基取代或未取代的萘基，Ar1-Ar3为独立地表示苯基，甲苯基，叔丁基苯基，萘基，吡啶基，甲基萘，联苯基，二苯基苯基，萘基苯基，二苯基联苯基，二芳香胺基苯基，N-苯基咔唑基，(9,9-二烷基)芴基，(9,9-二烷基取代或未取代苯基)芴基，9,9-螺芴基。
  4. 根据权利要求3所述的有机电子材料，其中，R3-R17优选为氢，R1，R2可以独立优选表示为氢，甲基，乙基，丙基，异丙基，叔丁基，苯基，萘基，或结合成芴基；Ar1-Ar3为独立地表示苯基，吡啶基，甲苯基，萘基，甲基萘，联苯基，二苯基苯基，萘基苯基，二苯基联苯基，(9,9-二烷基)芴基，(9,9-二甲基取代或未取代苯基)芴基，9,9-螺芴基。
  5. 根据权利要求4所述的有机电子材料，R3-R17优选为氢；R1，R2为独立地表示氢，甲基，或结合成芴基；Ar1，Ar2，Ar3为独立地表示苯基，萘基。
  6. 根据权利要求1所述的有机电子材料，为下列结构化合物：
    Figure PCTCN2015088709-appb-100002
    Figure PCTCN2015088709-appb-100003
    Figure PCTCN2015088709-appb-100004
    Figure PCTCN2015088709-appb-100005
    Figure PCTCN2015088709-appb-100006
    Figure PCTCN2015088709-appb-100007
    Figure PCTCN2015088709-appb-100008
    Figure PCTCN2015088709-appb-100009
    Figure PCTCN2015088709-appb-100010
    Figure PCTCN2015088709-appb-100011
    Figure PCTCN2015088709-appb-100012
    Figure PCTCN2015088709-appb-100013
    Figure PCTCN2015088709-appb-100014
    Figure PCTCN2015088709-appb-100015
    Figure PCTCN2015088709-appb-100016
    Figure PCTCN2015088709-appb-100017
    Figure PCTCN2015088709-appb-100018
    Figure PCTCN2015088709-appb-100019
    Figure PCTCN2015088709-appb-100020
    Figure PCTCN2015088709-appb-100021
    Figure PCTCN2015088709-appb-100022
    Figure PCTCN2015088709-appb-100023
    Figure PCTCN2015088709-appb-100024
    Figure PCTCN2015088709-appb-100025
    Figure PCTCN2015088709-appb-100026
    Figure PCTCN2015088709-appb-100027
    Figure PCTCN2015088709-appb-100028
  7. 根据权利要求6所述的有机电子材料，为下列结构化合物，
    Figure PCTCN2015088709-appb-100029
  8. 权利要求1-7任一所述有机电子材料在有机电致发光器件，有机太阳能电池，有机薄膜晶体管或有机光感受器领域的应用。
PCT/CN2015/088709 2015-03-09 2015-09-01 有机电子材料 WO2016141691A1 (zh)

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