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      A green polyol approach for the synthesis of Cu 2O NPs adhered on graphene oxide: a robust and efficient catalyst for 1,2,4-triazole and imidazo[1,2- a]pyridine synthesis

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          Abstract

          Cu 2O NPs immobilized on graphene oxide are used as a heterogeneous catalyst for the synthesis of a series of 1,2,4-triazoles and imidazo[1,2- a]pyridines under solvent-free conditions.

          Abstract

          A green “polyol method” is reported for the synthesis of Cu 2O nanoparticles (NPs) immobilized on graphene oxide (Cu 2O-GO), for the first time. The composition of the synthesised composite was characterized by FT-IR, Raman, PXRD, FESEM, high-resolution TEM, XPS, TGA and ICP-MS analysis. Its catalytic application, as a novel heterogeneous catalyst, has been investigated in the solvent-free synthesis of a series of pharmaceutically important heterocycles containing nitrogen, viz.1,2,4-triazoles and imidazo[1,2- a]pyridines. The composite shows an extensive substrate scope and broad functional group resilience. This green methodology involves the use of inexpensive reactants, moderate temperature, and solvent-free conditions and affords an excellent yield of products. The composite is retrieved from reaction mixtures by filtration and can be reused up to five cycles without any noticeable loss in its catalytic activity for both reactions.

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          Occurrence of the potent mutagens 2- nitrobenzanthrone and 3-nitrobenzanthrone in fine airborne particles

          Polycyclic aromatic compounds (PACs) are known due to their mutagenic activity. Among them, 2-nitrobenzanthrone (2-NBA) and 3-nitrobenzanthrone (3-NBA) are considered as two of the most potent mutagens found in atmospheric particles. In the present study 2-NBA, 3-NBA and selected PAHs and Nitro-PAHs were determined in fine particle samples (PM 2.5) collected in a bus station and an outdoor site. The fuel used by buses was a diesel-biodiesel (96:4) blend and light-duty vehicles run with any ethanol-to-gasoline proportion. The concentrations of 2-NBA and 3-NBA were, on average, under 14.8 µg g−1 and 4.39 µg g−1, respectively. In order to access the main sources and formation routes of these compounds, we performed ternary correlations and multivariate statistical analyses. The main sources for the studied compounds in the bus station were diesel/biodiesel exhaust followed by floor resuspension. In the coastal site, vehicular emission, photochemical formation and wood combustion were the main sources for 2-NBA and 3-NBA as well as the other PACs. Incremental lifetime cancer risk (ILCR) were calculated for both places, which presented low values, showing low cancer risk incidence although the ILCR values for the bus station were around 2.5 times higher than the ILCR from the coastal site.
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            Synthesis, properties, and applications of graphene oxide/reduced graphene oxide and their nanocomposites

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              A Review on Recent Advances in Nitrogen-Containing Molecules and Their Biological Applications

              The analogs of nitrogen-based heterocycles occupy an exclusive position as a valuable source of therapeutic agents in medicinal chemistry. More than 75% of drugs approved by the FDA and currently available in the market are nitrogen-containing heterocyclic moieties. In the forthcoming decade, a much greater share of new nitrogen-based pharmaceuticals is anticipated. Many new nitrogen-based heterocycles have been designed. The number of novel N-heterocyclic moieties with significant physiological properties and promising applications in medicinal chemistry is ever-growing. In this review, we consolidate the recent advances on novel nitrogen-containing heterocycles and their distinct biological activities, reported over the past one year (2019 to early 2020). This review highlights the trends in the use of nitrogen-based moieties in drug design and the development of different potent and competent candidates against various diseases.
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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                NJCHE5
                New Journal of Chemistry
                New J. Chem.
                Royal Society of Chemistry (RSC)
                1144-0546
                1369-9261
                May 03 2022
                2022
                : 46
                : 17
                : 8094-8104
                Affiliations
                [1 ]Department of Chemistry and Chemical Biology, Indian Institute of Technology (ISM), Dhanbad, 826004, India
                [2 ]Department of Chemistry, Faculty of Science, Dayalbagh Educational Institute, Dayalbagh, Agra, 282005, India
                Article
                10.1039/D2NJ00831A
                ec711436-c3bf-4d11-9223-3ae186f26a0d
                © 2022

                http://rsc.li/journals-terms-of-use

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