Hollow CeO<sub>2</sub> Nanospheres as Catalyst for the Conversion of Aromatic Diamines to Benzimidazoles

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Hollow CeO<sub>2</sub> Nanospheres as Catalyst for the Conversion of Aromatic Diamines to Benzimidazoles
Title:
Hollow CeO<sub>2</sub> Nanospheres as Catalyst for the Conversion of Aromatic Diamines to Benzimidazoles
Journal Title:
ACS Applied Nano Materials
Publication Date:
25 January 2024
Citation:
Srinivasappa, P. M., Singh, C., Alla, S. C., Gholap, S. S., Samal, A. K., Chaudhari, N. K., & Jadhav, A. H. (2024). Hollow CeO2 Nanospheres as Catalyst for the Conversion of Aromatic Diamines to Benzimidazoles. ACS Applied Nano Materials, 7(3), 2956–2970. https://doi.org/10.1021/acsanm.3c05323
Abstract:
Utilization of anthropogenic CO2 for the synthesis of valuable heterocyclic compounds is a very significant strategy to alleviate environmental issues. Herein, a hollow CeO2 nanosphere (HNS–CeO2) material made using solvothermal-method-assisted synthesis was employed as an efficient catalyst for the selective benzimidazole synthesis under neat and temperate reaction conditions. We examined the controlled reaction conditions for the design of the HNS–CeO2 material through the study of various reaction parameters. Very interestingly, the HNS–CeO2 material exhibited different surface morphological disparities due to the effect of various reaction parameters that were examined comprehensively using field emission scanning electron microscopy analysis. The HNS–CeO2 material was systematically well characterized using various analytical and spectroscopic techniques. The competent catalyst of HNS–CeO2 showed superior catalytic activity (100% conversion, 96% selectivity, and yield) under mild reaction conditions, and these conditions are successfully identified by studying the effect of various reaction parameters. Remarkably, the inherent properties of the HNS–CeO2 catalyst boosted the synergistic effect with the model reagents of o-phenylenediamine, carbon dioxide, dimethylamine borane (DMAB), and base. Moreover, different functional groups substituted benzimidazole compounds are successfully synthesized in good to excellent yields under optimized reaction conditions. The effective contributions of DMAB, base, Lewis acidic, and Lewis basic sites were successfully revealed by proposing a tentative benzimidazole reaction mechanism. Notably, the examined 15 successive recycles with stable catalytic activity performance demonstrated the stable catalytic activity and structural and physicochemical properties of the HNS–CeO2 catalyst.
License type:
Publisher Copyright
Funding Info:
The authors would like to acknowledge the Science and Engineering Research Board (SERB), Government of India, for financial support through Core Research Grant (CRG) File no. ACS Applied Nano Materials CRG/2021/000656. We also would like to acknowledge Jain University for partial research funding support.
Description:
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Applied Nano Materials, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acsanm.3c05323
ISSN:
2574-0970
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