Issue 51, 2021

Scholl reaction as a powerful tool for the synthesis of nanographenes: a systematic review

Abstract

Nanographenes, or extended polycyclic aromatic hydrocarbons, have been attracting increasing attention owing to their widespread applications in organic electronics. However, the atomically precise fabrication of nanographenes has thus far been achieved only through synthetic organic chemistry. Polycyclic aromatic hydrocarbons (PAHs) are popular research subjects due to their high stability, rigid planar structure, and characteristic optical spectra. The recent discovery of graphene, which can be regarded as giant PAH, has further stimulated research interest in this area. Chemists working with nanographene and heterocyclic analogs thereof have chosen it as their preferred tool for the assembly of large and complex architectures. The Scholl reaction has maintained significant relevance in contemporary organic synthesis with many advances in recent years and now ranks among the most useful C–C bond-forming processes for the generation of the π-conjugated frameworks of nanographene or their heterocyclic analogs. A broad range of oxidants and Lewis acids have found use in Scholl-type processes, including Cu(OTf)2/AlCl3, FeCl3, MoCl5, PIFA/BF3–Et2O, and DDQ, in combination with Brønsted or Lewis acids, and the surface-mediated reaction has found especially wide applications in PAH synthesis. Undoubtedly, the utility of the Scholl reaction is supreme in the construction of nanographene and their heterocyclic analogues. The detailed analysis of the progress achieved in this field reveals that many groups have contributed by pushing the boundary of structural possibilities, expanding into surface-assisted cyclodehydrogenation and developing new reagents. In this review, we highlight and discuss the recent modifications in the Scholl reaction for nanographene synthesis using numerous oxidant systems. In addition, the merits or demerits of each oxidative reagent is described herein.

Graphical abstract: Scholl reaction as a powerful tool for the synthesis of nanographenes: a systematic review

Article information

Article type
Review Article
Submitted
04 aug 2021
Accepted
10 sep 2021
First published
29 sep 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 32158-32202

Scholl reaction as a powerful tool for the synthesis of nanographenes: a systematic review

R. S. Jassas, E. U. Mughal, A. Sadiq, R. I. Alsantali, M. M. Al-Rooqi, N. Naeem, Z. Moussa and S. A. Ahmed, RSC Adv., 2021, 11, 32158 DOI: 10.1039/D1RA05910F

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