Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Triarylamine polymer, preparation method and application thereof

A technology of polymer and triarylamine, which is applied in the field of triarylamine polymer and its preparation, can solve the problems of limited use, low glass transition temperature, hole mobility, etc.

Pending Publication Date: 2021-09-10
杭州领挚科技有限公司
View PDF6 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, because of the relatively low glass transition temperature (T g ) and hole mobility, which limits its use in organic optoelectronic devices

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Triarylamine polymer, preparation method and application thereof
  • Triarylamine polymer, preparation method and application thereof
  • Triarylamine polymer, preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0213] Embodiment 1——Preparation of 3-trifluoromethoxy polytriphenylamine

[0214] 1. Preparation of Monomer 3-Trifluoromethoxytriphenylamine

[0215] In an open round bottom flask equipped with a magnetic stirrer and a thermometer, add 5 g of diphenylamine, 12.8 g of m-iodotrifluoromethoxybenzene, 1.5 mmol of palladium acetate, 6.2 g of potassium carbonate, and 250 mL of dimethyl sulfoxide (DMSO ) solvent, oscillating and mixing evenly and then warming up to 120°C and stirring the reaction under air, monitoring the reaction progress with TLC, stopping heating after the reaction is complete, quenching the reaction with saturated ammonium chloride solution after the mixture in the round bottom flask is cooled, and reacting After the mixture was extracted, dried, and concentrated under reduced pressure, the crude product obtained was separated and purified by column chromatography, and the eluent used was petroleum ether. The column chromatography eluate containing the product...

Embodiment 2

[0231] Embodiment 2——Preparation of 3-trifluoromethyl polytriphenylamine

[0232] 1. Preparation of Monomer 3-Trifluoromethyltriphenylamine

[0233] In an open round bottom flask equipped with a magnetic stirrer and a thermometer, add 4.96g of diphenylamine, 11.98g of m-iodobenzobenzotrifluoride, 1.5mmol of palladium acetate, 6.1g of potassium carbonate and 200mL of dimethylsulfoxide (DMSO) solvent , oscillate and mix evenly, heat up to 120°C and stir the reaction under air, monitor the reaction progress with TLC, stop heating after the reaction is complete, quench the reaction with saturated ammonium chloride solution after the mixture in the round bottom flask is cooled, and the reaction mixture The crude product obtained after extraction, drying, and concentration under reduced pressure is separated and purified by column chromatography, and the eluent used is petroleum ether. The column chromatography eluate containing the product is collected and concentrated to obtain ...

Embodiment 3

[0248] Embodiment 3——Preparation of 4-trifluoromethoxy polytriphenylamine

[0249] 1. Preparation of monomer 4-trifluoromethoxytriphenylamine

[0250] In an open round bottom flask equipped with a magnetic stirrer and a thermometer, add 5.1 g of diphenylamine, 13.06 g of p-bromotrifluoromethoxybenzene, 1.5 mmol of palladium acetate, 6.46 g of potassium carbonate and 200 mL of dimethyl sulfoxide ( DMSO) solvent, oscillating and mixing evenly, then warming up to 125°C and stirring the reaction under air, monitoring the progress of the reaction with TLC, stopping the heating after the reaction is complete, and quenching the reaction with saturated ammonium chloride solution after the mixture in the round bottom flask is cooled. The crude product obtained after the reaction mixture was extracted, dried, and concentrated under reduced pressure was separated and purified by column chromatography, and the eluent used was petroleum ether. The column chromatography eluate containing ...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
Hole mobilityaaaaaaaaaa
Hole mobilityaaaaaaaaaa
Hole mobilityaaaaaaaaaa
Login to View More

Abstract

The invention discloses a triarylamine polymer and application thereof. The triarylamine polymer has a structural general formula shown in the following formula (I), wherein the definition of substituent groups in the formula (I) is the same as that in the specification. According to the invention, the triarylamine polymer has good stability and hole mobility, and can be used as a hole transport material to be applied to a quantum dot light-emitting device (QLED), an organic light-emitting device (OLED) and a perovskite solar cell (PSC).

Description

technical field [0001] This application relates to but not limited to the field of organic optoelectronic materials, in particular to a triarylamine polymer and its preparation method and application. Background technique [0002] Triarylamine small molecular compound is an electron-rich compound with π-conjugated structure. Its nitrogen atom easily loses electrons to form cationic radicals. Therefore, this compound has relatively good electron-donating properties and can be widely used as a hole-transporting material. In organic photoelectric devices, such as quantum dot light-emitting diodes (Quantum Dot Light Emitting Diodes, QLED), organic electroluminescent diodes (Organic Light-Emitting Diode, OLED), perovskite solar cells (Perovskite Solar Cells, PSC), etc. However, because of the relatively low glass transition temperature (T g ) and hole mobility, which limit its use in organic optoelectronic devices. [0003] In recent years, the application and research of optoe...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): C08G61/12H01L51/50H01L51/54H01L51/42H01L51/46
CPCC08G61/12C08G2261/411C08G2261/512C08G2261/122C08G2261/522C08G2261/11C08G2261/1434C08G2261/146C08G2261/1412H10K85/151H10K30/10H10K50/115H10K50/15Y02E10/549
Inventor 冯林润刘哲杜江文李骏
Owner 杭州领挚科技有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com