Compound containing cyanobenzene or thiocyanobenzene, and applications in organic electroluminescent devices

A technology of thiocyanobenzene and compounds, which can be used in electric solid devices, electrical components, light-emitting materials, etc., can solve problems such as differences, and achieve the effects of avoiding aggregation, good industrialization prospects, and good film-forming properties.

Active Publication Date: 2019-06-21
JIANGSU SUNERA TECH CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In addition, for the collocation of OLED devices with different structures, the photoelectric functional materials used have strong selectivity, and the performance of the same material in devices with different structures may be completely different.

Method used

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  • Compound containing cyanobenzene or thiocyanobenzene, and applications in organic electroluminescent devices
  • Compound containing cyanobenzene or thiocyanobenzene, and applications in organic electroluminescent devices
  • Compound containing cyanobenzene or thiocyanobenzene, and applications in organic electroluminescent devices

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0043] Embodiment 1: the synthesis of intermediate M:

[0044]

[0045] (1) Dissolve raw material B and raw material C in a mixed solution of toluene and ethanol, add Pd(PPh 3 ) 4 and K 2 CO 3 , react at 95-110°C for 10-24 hours under an inert atmosphere, monitor the reaction process with TLC during the reaction process, cool and filter the raw materials after the reaction is complete, spin the filtrate to remove the solvent, and pass the crude product through a silica gel column to obtain Intermediate S; the consumption of described toluene and ethanol is to use 30~50mL toluene and 5~10mL ethanol per gram of raw material C, the molar ratio of raw material B and raw material C is (1~1.5):1, Pd(PPh 3 ) 4 The molar ratio with raw material C is (0.006~0.02):1, K 2 CO 3 The molar ratio with raw material C is (1.5~2):1.

[0046] (2) Under the protection of nitrogen, weigh 0.01mol of intermediate S and dissolve it in 150ml of tetrahydrofuran, cool to -78°C, then add 1.6mol...

Embodiment 2

[0056] Embodiment 2: the synthesis of compound 1:

[0057]

[0058] In a 250mL three-necked flask, dissolve 0.01mol of raw material A-1 and 0.012mol of raw material B-1 in 150mL of toluene and ethanol (V 甲苯 :V 乙醇 =5:1) In the mixed solution, add 0.0002mol Pd(PPh 3 ) 4 and 0.02mol K 2 CO 3 , reacted at 110°C for 24 hours under an inert atmosphere, and continuously monitored the reaction process with TLC during the reaction process. After the raw materials were completely reacted, cooled and filtered, the filtrate was rotary evaporated to remove the solvent, and the crude product was passed through a silica gel column to obtain the target product; element Analytical structure (molecular formula C 36 h 23 N 3 ): theoretical value C, 86.90; H, 4.66; N, 8.44; test value: C, 86.95; H, 4.72; N, 8.47; for 497.23.

Embodiment 3

[0059] Embodiment 3: the synthesis of compound 3:

[0060]

[0061] In a 250mL three-neck flask, dissolve 0.01mol of raw material A-1 and 0.012mol of raw material B-4 in 150mL of toluene and ethanol (V 甲苯 :V 乙醇 =5:1) In the mixed solution, add 0.0002mol Pd(PPh 3 ) 4 and 0.02mol K 2 CO 3 , reacted at 110°C for 24 hours under an inert atmosphere, and continuously monitored the reaction process with TLC during the reaction process. After the raw materials were completely reacted, cooled and filtered, the filtrate was rotary evaporated to remove the solvent, and the crude product was passed through a silica gel column to obtain the target product; element Analytical structure (molecular formula C 36 h 23 N 3 S): theoretical value C,81.64; H,4.38; N,7.93; S,6.05; test value: C,81.67; H,4.39; N,7.97; S,6.08; ): The theoretical value is 529.16, and the measured value is 529.18.

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Abstract

The invention discloses a compound containing cyanobenzene or thiocyanobenzene, and applications in organic electroluminescent devices. According to the present invention, the compound comprises a cyanobenzene or thiocyanobenzene group, has deep HOMO energy level and high hole mobility, and can be used as a hole blocking material or electron transporting material; the compound has the structure containing the hole group so as to balance the electron and the hole of the material, such that the material can be used as the electron-biased light emitting layer host material; the compound has the group with strong rigidity, and further has characteristics of less intermolecular crystallization, less aggregation and good film forming property; and with the application of the compound as the organic electroluminescent function layer material in OLED devices, the current efficiency, the power efficiency and the external quantum efficiency of the device are greatly improved, and the service life of the device is significantly prolonged.

Description

technical field [0001] The invention relates to the technical field of semiconductors, in particular to a compound containing cyanobenzene or thiocyanobenzene and its application in organic electroluminescent devices. Background technique [0002] Organic electroluminescent (OLED: Organic Light Emission Diodes) device technology can be used to manufacture new display products and also can be used to make new lighting products, which is expected to replace the existing liquid crystal display and fluorescent lighting, and has a wide application prospect. The OLED light-emitting device is like a sandwich structure, including electrode material film layers, and organic functional materials sandwiched between different electrode film layers. Various functional materials are superimposed on each other according to the application to form an OLED light-emitting device. As a current device, when a voltage is applied to the electrodes at both ends of the OLED light-emitting device, a...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07D471/04C09K11/06H01L51/54
Inventor 王芳李崇张兆超张小庆蔡啸
Owner JIANGSU SUNERA TECH CO LTD
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