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

Year: 2021
Type: review
Abstract: O, 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.
Source: RSC Advances
DOI: 10.1039/d1ra05910f
Authors: Rabab S. Jassas, Ehsan Ullah Mughal, Amina Sadiq, Reem I. Alsantali, Munirah M. Al-Rooqi, Nafeesa Naeem, Ziad Moussa, Saleh A. Ahmed
Institutions: Umm al-Qura University, University of Gujrat, Government College Women University Sialkot, Taif University, United Arab Emirates University, Assiut University
Language: English
Field: Chemistry
Open Access status: gold
Estimated APC paid: $1,042
OpenAlex ID: W3204963396
FWCI: 1.231
Cites: 157
Cited by: 103
Related to: 10