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

IF 5.8 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Sobia Mukhtar , Ayesha Rafiq , Syed Ali Raza Naqvi , Sana Aslam , Matloob Ahmad , Sami A. Al-Hussain , Magdi E.A. Zaki
{"title":"Synthetic routes for N-arylation of carbazole derivatives and their applications as organic materials","authors":"Sobia Mukhtar ,&nbsp;Ayesha Rafiq ,&nbsp;Syed Ali Raza Naqvi ,&nbsp;Sana Aslam ,&nbsp;Matloob Ahmad ,&nbsp;Sami A. Al-Hussain ,&nbsp;Magdi E.A. Zaki","doi":"10.1016/j.jscs.2024.101927","DOIUrl":null,"url":null,"abstract":"<div><p>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 <em>etc</em>. Synthesis of <em>N</em>-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 <em>N</em>-arylated carbazoles have unique properties such as high thermal stability, wide band gap, and excellent electrical and optical properties. The methods used for the <em>N</em>-arylation of carbazoles include transition metal-catalyzed reactions and metal-free reactions. The most common and classical methods for the <em>N</em>-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 <em>N</em>-arylation of carbazoles and their applications.</p></div>","PeriodicalId":16974,"journal":{"name":"Journal of Saudi Chemical Society","volume":"28 5","pages":"Article 101927"},"PeriodicalIF":5.8000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1319610324001224/pdfft?md5=8039eeafa4fb9e9017fa7366811f0015&pid=1-s2.0-S1319610324001224-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Saudi Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1319610324001224","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

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 Image

咔唑衍生物的 N-芳基化合成路线及其作为有机材料的应用
咔唑是一种杂环芳香族有机化合物,在医药、生物和材料科学领域有着广泛的应用。咔唑衍生物具有多种生物活性,如抗生素、消炎、抗肿瘤和抗氧化等。由于 N-芳基咔唑在有机发光二极管、染料敏化太阳能电池和其他有机电子产品中的应用,其合成已成为科学家们关注的一个重要领域。N- 芳基化咔唑具有独特的性能,如高热稳定性、宽带隙以及优异的电学和光学性能。用于咔唑 N-芳基化的方法包括过渡金属催化反应和无金属反应。铜催化的乌尔曼偶联反应是最常见、最经典的咔唑 N-芳基化方法,同时也使用钯、镍和铁催化剂。本综述重点介绍用于咔唑 N-芳基化的所有合成方法及其应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Saudi Chemical Society
Journal of Saudi Chemical Society CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
8.90
自引率
1.80%
发文量
120
审稿时长
38 days
期刊介绍: Journal of Saudi Chemical Society is an English language, peer-reviewed scholarly publication in the area of chemistry. Journal of Saudi Chemical Society publishes original papers, reviews and short reports on, but not limited to: •Inorganic chemistry •Physical chemistry •Organic chemistry •Analytical chemistry Journal of Saudi Chemical Society is the official publication of the Saudi Chemical Society and is published by King Saud University in collaboration with Elsevier and is edited by an international group of eminent researchers.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信