Open Access

Nano-sulfonated Graphene Oxide: A Metal-free Catalyst for the Synthesis of Benzimidazoles and Antimicrobial Activities

Murali Krishna Madasu V, shalemcml@gmail.com
Department of Engineering Chemistry, Andhra University College of Engineering, Andhra University, Visakhapatnam, AP, India
ORCID
Padma M, mpadma.aueng@gmail.com
Department of Engineering Chemistry, Andhra University College of Engineering, Andhra University, Visakhapatnam, AP, India
Jyotsna Cherukuri, jyotsnacherukuri@gmail.com
Department of Chemistry, VNR Vignana Jyothi Institute of Engineering and Technology, Hyderabad, TG, India
Kadali Yashoda, yashoda.kadali@gmail.com
Department of Chemistry, Vignan Institute of Information Technology (A), Duvvada, Visakhapatnam, AP, India
Vijaya E, enagandula.vijaya@gmail.com
Department of H and S, CMR Technical Campus, Hyderabad, TG, India
Praveen CH, pchoppara@gmail.com
Department of Chemistry, Pithapur Rajah’s Government College(A), Kakinada, AP, India
Manuri Brahmayya brahma.orgchem@gmail.com
Department of Chemistry, VNR Vignana Jyothi Institute of Engineering and Technology, Hyderabad, TG, India
ORCID



J. Environ. Nanotechnol., Volume 15, No 1 (March 2026) pp. 701-715

https://doi.org/10.13074/jent.2026.03.2612109

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Abstract

Nano sulfonated graphene oxide (SGO) was synthesized with slight modifications to previously reported methods. An efficient and ecofriendly protocol was developed for the synthesis of benzimidazole derivatives using o-phenylenediamine and D-glucose as substrates, employing a metal-free sulfonated graphene oxide carbocatalyst. A diverse range of benzimidazole derivatives was obtained in moderate to high yields (up to 94%) using a sustainable and readily available C1 source under sonication conditions. The reaction, carried out in ethanol with tertiary-butyl hydroperoxide, provides a general and novel approach for benzimidazole synthesis via a carbonylation pathway. The process is facilitated by a cost-effective and environmentally benign SGO nanocatalyst, enabling the formation of valuable products in excellent yields. The synthesized benzimidazole derivatives exhibited strong antibacterial activity, with inhibition rates of 99% to 100% against Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, and Streptococcus pyogenes.

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