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Synthetic routes for N-arylation of carbazole derivatives and their applications as organic materials.
- Source :
- Journal of Saudi Chemical Society; Sep2024, Vol. 28 Issue 5, pN.PAG-N.PAG, 1p
- Publication Year :
- 2024
-
Abstract
- [Display omitted] Carbazole is a heterocyclic aromatic organic compound that has vast applications in pharmaceuticals, and in biological and material sciences. Carbazole derivatives show various biological activities such as antibiotic, anti-inflammatory, anti-tumor and anti-oxidant activities etc. Synthesis of N -arylated carbazoles has become a major area of interest for scientists due to their applications in organic light-emitting diodes, dye-sensitized solar cells, and other organic electronics. The N -arylated carbazoles have unique properties such as high thermal stability, wide band gap, and excellent electrical and optical properties. The methods used for the N -arylation of carbazoles include transition metal-catalyzed reactions and metal-free reactions. The most common and classical methods for the N -arylation of carbazoles are copper-catalyzed Ullmann coupling reactions, while palladium, nickel, and iron catalysts are also used. This review focuses on all the synthetic methods used for the N -arylation of carbazoles and their applications. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 13196103
- Volume :
- 28
- Issue :
- 5
- Database :
- Supplemental Index
- Journal :
- Journal of Saudi Chemical Society
- Publication Type :
- Academic Journal
- Accession number :
- 179948643
- Full Text :
- https://doi.org/10.1016/j.jscs.2024.101927