D-A-type polymer containing S,S-dioxy-dibenzothiophene in main chain as well as preparation method and application thereof

A technology of dibenzothiophene and polymer, applied in the field of D-A type polymer and its preparation, can solve problems such as limiting electroluminescence efficiency, and achieve the effects of being beneficial to device efficiency, increasing the generation ratio, and promoting the crossing process

Active Publication Date: 2018-03-06
东莞伏安光电科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, traditional polymer fluorescent materials can only utilize 25% of singlet excitons, and 75% of triplet excitonic energy is lost through non-radiative t

Method used

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  • D-A-type polymer containing S,S-dioxy-dibenzothiophene in main chain as well as preparation method and application thereof
  • D-A-type polymer containing S,S-dioxy-dibenzothiophene in main chain as well as preparation method and application thereof
  • D-A-type polymer containing S,S-dioxy-dibenzothiophene in main chain as well as preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0034] Embodiment 1: the preparation of compound M1

[0035] (1) Preparation of compound 1

[0036] Add 2,8-dibromo-S, S-dioxy-dibenzothiophene (3.74g, 10mmol), aniline (2.79g, 30mmol), sodium tert-butoxide (4.81g, 50mmol) into a 100ml two-necked flask, Tris(dibenzylideneacetone)dipalladium (458 mg, 0.5 mmol), tri-tert-butylphosphine (101 mg, 0.5 mmol) and 50 ml of toluene were heated to 100° C. for 12 hours under nitrogen. After the reaction was completed, the product was extracted with dichloromethane, the organic phase was washed with saturated aqueous sodium chloride solution, the solvent was evaporated under reduced pressure, and the crude product was eluted with a mixed solvent of petroleum ether:dichloromethane=3:1 (v / v) Purified by solvent column chromatography to obtain 1.60 g of white solid with a yield of 40%, (mass spectrum: 398.2).

[0037] (2) Preparation of compound M1

[0038]Add compound 1 (398.5g, 10mmol), p-bromoiodobenzene (8.49g, 30mmol), sodium tert-bu...

Embodiment 2

[0041] Embodiment 2: the preparation of compound M2

[0042] Add 2,8-diiodo-S, S-dioxo-dibenzothiophene (4.68g, 10mmol), 3-bromocarbazole (6.15g, 25mmol), potassium carbonate (6.9g, 50mmol) into a 100ml two-necked flask ), cuprous iodide (95mg, 0.5mmol) and 50ml of toluene were heated to 100°C for 12 hours under nitrogen atmosphere. After the reaction was completed, the product was extracted with dichloromethane, the organic phase was washed with saturated aqueous sodium chloride solution, the solvent was evaporated under reduced pressure, and the crude product was eluted with a mixed solvent of petroleum ether:dichloromethane=4:1 (v / v) Purified by solvent column chromatography to obtain 2.59 g of white solid with a yield of 37%, (mass spectrum: 704.0).

[0043] The chemical reaction equation is shown in formula (3):

[0044]

Embodiment 3

[0046] Preparation of compound M3

[0047] Under a nitrogen atmosphere, add 3,6-dibromocarbazole (3.25g, 10mmol), 2-ethylbromohexane (2.90g, 15mmol), potassium carbonate (4.14g, 30mmol) to a 300ml two-necked flask ) and 150ml N,N-dimethylformamide were stirred and reacted at 80°C for 12 hours. After cooling, the product was extracted with dichloromethane, washed five times with saturated aqueous sodium chloride solution until the water layer was clear, distilled off under reduced pressure to remove dichloromethane, and the crude product was purified by column chromatography using petroleum ether as eluent to obtain a colorless transparent liquid 3.94 g, yield 90%, (mass spectrum: 437.1).

[0048] Preparation of Compound M4

[0049] Under nitrogen protection, add M3 (4.37g, 10mmol), pinacol diborate (6.35g, 25mmol), [1,1'-bis(diphenylphosphino)ferrocene] into a 300ml two-necked flask Palladium dichloride (0.49g, 0.5mmol), potassium acetate (3.92g, 40mmol) and 120ml of dioxan...

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Abstract

The invention discloses a D-A-type polymer containing S,S-dioxy-dibenzothiophene in a main chain as well as a preparation method and application thereof. An electricity-absorbing S,S-dioxy-dibenzothiophene unit and a power supply unit are adopted to copolymerize to form a D-A structure molecule, and obtain the D-A-type polymer containing S,S-dioxy-dibenzothiophene in the main chain. The 2,8-carbonatoms of the S,S-dioxy-dibenzothiophene unit are connected with a nitrogen-containing aromatic heterocyclic unit of the power supply through a C-N bond, and a twist angle of a D-A unit is larger andis beneficial to reduce degree of conjugation of polymer molecules, effective separation of HOMO and LUMO electron clouds is achieved, singlet state-triplet state energy level difference is reduced, promotion of intermolecular inversion intersystem crossing is improved, and ratio of singlet exciton generation is increased, and device efficiency is improved. The D-A-type polymer containing S,S-dioxy-dibenzothiophene in the main chain has good solubility and can be used for preparing a light emitting layer of a polymer light emitting diode.

Description

technical field [0001] The invention belongs to the field of organic photoelectric technology, and specifically relates to a D-A type polymer containing S,S-dioxy-dibenzothiophene in the main chain, a preparation method and application thereof. Background technique [0002] In 1990, the Cavendish Laboratory of the University of Cambridge published a polymer thin-film electroluminescent device prepared by using conjugated polymer PPV, which officially opened the prelude to the research on polymer light-emitting diodes (PLEDs). Compared with small molecule light-emitting diodes, polymer light-emitting diodes have the following advantages: (1) large-area thin films can be prepared by printing, inkjet printing, etc.; (3) The modification of the conjugated polymer can avoid crystallization and improve the stability of the device. [0003] The PLED device is composed of a cathode, an anode, and an organic layer in the middle. The organic layer generally includes an electron trans...

Claims

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Application Information

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IPC IPC(8): C08G61/12H01L51/50H01L51/54
CPCC08G61/124C08G61/126C08G2261/3241C08G2261/3243C08G2261/124C08G2261/1412C08G2261/95C08G2261/522C08G2261/411H10K85/113H10K50/11H10K2101/10
Inventor 应磊彭沣胡黎文黄飞曹镛
Owner 东莞伏安光电科技有限公司
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