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Synthetic routes for N-arylation of carbazole derivatives and their applications as organic materials.

Authors :
Mukhtar, Sobia
Rafiq, Ayesha
Naqvi, Syed Ali Raza
Aslam, Sana
Ahmad, Matloob
Al-Hussain, Sami A.
Zaki, Magdi E.A.
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