Issue 34, 2025

Traditional and photocatalytic conversion of aniline into azocompounds – a comprehensive experimental and theoretical review

Abstract

The catalytic conversion of aniline into azo compounds represents a significant and versatile route in synthetic organic chemistry, with applications spanning dyes, pharmaceuticals, and functional materials. This comprehensive review systematically examines recent advances in catalytic strategies for azo bond formation from aniline derivatives, encompassing homogeneous, heterogeneous, enzymatic, and photo-redox catalysis. Key mechanistic pathways, including oxidative coupling, dehydrogenative aromatization, and redox processes, are critically analyzed. The influence of catalyst design (e.g., transition metals, organo-catalysts, nanomaterials) and reaction conditions (solvent, oxidants, temperature) on selectivity and efficiency is discussed. Additionally, the review highlights sustainable approaches, such as aerobic oxidation and visible-light-driven catalysis, aligning with green chemistry principles. Challenges, including substrate scope limitations and scalability, are addressed, along with emerging trends and future prospects for industrial and academic applications. This work aims to serve as a foundational resource for researchers exploring catalytic azo compound synthesis.

Graphical abstract: Traditional and photocatalytic conversion of aniline into azocompounds – a comprehensive experimental and theoretical review

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Article information

Article type
Review Article
Submitted
30 May 2025
Accepted
28 Jul 2025
First published
08 Aug 2025
This article is Open Access
Creative Commons BY license

RSC Adv., 2025,15, 28231-28239

Traditional and photocatalytic conversion of aniline into azocompounds – a comprehensive experimental and theoretical review

A. Khan, H. Ran, C. Saisai, N. Muhammad, A. Abbas, Z. Yi, F. Shah, W. Chen and D. Xu, RSC Adv., 2025, 15, 28231 DOI: 10.1039/D5RA03828F

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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