The design, synthesis and performance of thermally activated delayed fluorescence macromolecules

Literature Information

Publication Date 2020-02-07
DOI 10.1039/D0PY00096E
Impact Factor 5.582
Authors

Tingcong Jiang, Yuchao Liu, Zhongjie Ren


View Original

Abstract

Since the first application of thermally activated delayed fluorescence (TADF) materials in organic light emitting diodes (OLEDs), rapid development and huge progress have been made. At present, the reported TADF materials with high device performance can achieve electroluminescence (EL) with emission colors nearly covering the whole visible ranges. Following the design strategy for TADF small molecules, many macromolecular emitters with different emission colors have been reported to date. Nevertheless, there are realistically a lot of hurdles to surmount when developing low-cost displays and lighting products using macromolecules through the wet processing technology. It confirmedly engrossed us to depict the correlation between emission colors and molecular structures or fabrication of OLED devices in depth. In this context, this review has been written to provide an overview on the TADF mechanism, the design strategy of TADF macromolecules and typical solution-processed polymeric and dendritic emitters organized herein as a function of EL emission colors.

Related Literature

Inherently chiral cone-calix[4]arenes via a subsequent upper rim ring-closing/opening methodology

José Augusto Berrocal, Matthew B. Baker, Laura Baldini, Alessandro Casnati, Stefano Di Stefano

2018-09-22 Paper

DOI: 10.1039/C8OB01813H

A donor–acceptor substituted molecular motor: unidirectional rotation driven by visible light

Richard A. van Delden, Nagatoshi Koumura, Annemarie Schoevaars, Auke Meetsma, Ben L. Feringa

2002-11-08 Communication

DOI: 10.1039/B209378B

The selective functionalisation and difunctionalisation of p-substituted calix[6]arene and calix[8]arenes using hydrophilic moieties

Gwénaëlle Hervé, Dirk Uwe Hahn, Anne-Cécile Hervé, Kerry J. Goodworth, Alison M. Hill, Helen C. Hailes

2002-12-19 Paper

DOI: 10.1039/B208649M

Cyclopropanation of alkenes with metallocarbenes generated from monocarbonyl iodonium ylides

Tristan Chidley, Graham K. Murphy

2018-10-25 Communication

DOI: 10.1039/C8OB02636J

Manganese catalyzed N-alkylation of anilines with alcohols: ligand enabled selectivity

Vinod G. Landge, Akash Mondal, Vinit Kumar, Avanashiappn Nandakumar, Ekambaram Balaraman

2018-10-08 Paper

DOI: 10.1039/C8OB01886C

Transition metal free decarboxylative fluoroalkylation of N-acrylamides with 3,3,3-trifluoro-2,2-dimethylpropanoic acid (TFDMPA)

Yingkun Shi, Hongqing Xiao, Xiu-Hua Xu, Yangen Huang

2018-10-22 Communication

DOI: 10.1039/C8OB02457J

Tetracyclic pyrazine-fused furazans as insensitive energetic materials: syntheses, structures, and properties

Qi Sun, Xin Li, Qiuhan Lin, Ming Lu

2018-10-11 Communication

DOI: 10.1039/C8OB02155D

Synthesis of stereochemically-biased spiropyrans by microwave-promoted, one-pot alkylation–condensation

Alexis Perry, Kane Davis, Lara West

2018-09-21 Paper

DOI: 10.1039/C8OB01996G

You might also like

Compound Q&A

Is 4-Benzyl-2,2-dimethylmorpholine (CAS: 84761-04-6) safe?

4-Benzyl-2,2-dimethylmorpholine is generally considered safe when handled under ...

84761-04-64-Benzyl-2,2-dimethy...
Compound Q&A

What is (5,6-Dimethoxy-3-pyridinyl)boronic acid (CAS: 1346526-61-1)?

(5,6-Dimethoxy-3-pyridinyl)boronic acid is a chemical compound with the molecula...

1346526-61-1(5,6-Dimethoxy-3-pyr...
Compound Q&A

How is 1,1,3,3-Tetramethyl-1,3-bis(2-methyl-2-propanyl)disiloxane (CAS: 67875-55-2) typically synthesized?

1,1,3,3-Tetramethyl-1,3-bis(2-methyl-2-propanyl)disiloxane is synthesized throug...

67875-55-21,1,3,3-Tetramethyl-...
Compound Q&A

What are the main uses of (2R,4S)-1-Boc-4-methylpyrrolidine-2-carboxylic acid (CAS: 1018818-04-6)?

(2R,4S)-1-Boc-4-methylpyrrolidine-2-carboxylic acid is primarily used as a build...

1018818-04-6(2R,4S)-1-Boc-4-meth...
Compound Q&A

What precautions should be taken when handling 2,3-Dichloroacrylonitrile (CAS: 22410-58-8)?

When handling 2,3-Dichloroacrylonitrile, it is crucial to wear appropriate perso...

22410-58-82,3-Dichloroacryloni...
Compound Q&A

How should (S)-1-(o-Tolyl)ethanamine hydrochloride (CAS: 1332832-16-2) be stored?

(S)-1-(o-Tolyl)ethanamine hydrochloride should be stored in a cool, dry place to...

1332832-16-2(S)-1-(o-Tolyl)ethan...
Compound Q&A

What are the physical and chemical properties of Benzyl [1-(hydroxyamino)-1-imino-2-methyl-2-propanyl]carbamate (CAS: 518047-98-8)?

Benzyl [1-(hydroxyamino)-1-imino-2-methyl-2-propanyl]carbamate (CAS: 518047-98-8...

518047-98-8Benzyl [1-(hydroxyam...
Compound Q&A

What industries use 2-Methyloxazole-5-carbaldehyde (CAS: 885273-42-7)?

2-Methyloxazole-5-carbaldehyde is used in the pharmaceutical industry for the sy...

885273-42-72-Methyloxazole-5-ca...
Compound Q&A

What is the market or research trend for 2-Methyl-2-propanyl 4-[(1S)-1-hydroxyethyl]-1-piperidinecarboxylate (CAS: 389889-82-1)?

The market for 2-Methyl-2-propanyl 4-[(1S)-1-hydroxyethyl]-1-piperidinecarboxyla...

389889-82-12-Methyl-2-propanyl ...
Compound Q&A

Is 1-Butyl-3-methylpyridinium bromide (CAS: 26576-85-2) safe?

1-Butyl-3-methylpyridinium bromide is generally considered safe for laboratory u...

26576-85-21-Butyl-3-methylpyri...

Source Journal

Polymer Chemistry

Polymer Chemistry
CiteScore: 8.6
Self-citation Rate: 7.3%
Articles per Year: 457

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.