4.6 Article

In-situ formation of Ag NPs on the ribonic ?-lactone-modified UiO-66-NH2: An effective catalyst for organic synthesis and antibacterial applications

期刊

PROCESS BIOCHEMISTRY
卷 122, 期 -, 页码 149-165

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ELSEVIER SCI LTD
DOI: 10.1016/j.procbio.2022.08.031

关键词

Metal-organic frameworks; UiO-66-NH2; Ag nanoparticles; Catalytic reduction; Cyanation; Antibacterial

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  1. Razi University

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In this study, a porous heterogeneous catalyst was prepared via green deposition of silver nanoparticles on the surface of a functionalized metal-organic framework. The catalyst showed effective catalytic activity for the reduction of 4-nitrophenol and cyanation of aryl halides, as well as prominent antibacterial activity against Staphylococcus aureus and Escherichia coli.
Using of eco-friendly, cost-effective, and durable compounds as reducing and stabilizing reagents for metallic nanoparticles (MNPs) has always been alluring for the preparation of nanocatalysts. Herein, a porous hetero-geneous catalyst was prepared via green deposition of Ag NPs on the surface of functionalized metal-organic framework (MOF), Zr-UiO-66-NH2. Initially, UiO-66-NH2 was modified with D-(+)-ribonic gamma-lactone (RL), as a class of carbohydrates (CHs), which provides plenty of hydroxyl groups on the surface for reducing Ag+ ions and stabilizing Ag NPs. The catalytic activity of UiO-66-NH-RL-Ag was tested for the reduction of 4-nitrophenol in the presence of NaBH4 and the cyanation of aryl halides, for the first time, in the presence of nontoxic cyanating source K4[Fe(CN)6].3 H2O. The nanocatalyst effectively reduced 4-nitrophenol with a turnover frequency (TOF) of 333.2 h(-1). The kinetic studies illustrated that the reaction follows a pseudo-first-order kinetic. Moreover, UiO-66-NH-RL-Ag exhibited good catalytic activity with high efficiencies in the synthesis of various aryl nitriles. Furthermore, UiO-66-NH-RL-Ag showed a prominent antibacterial activity and inhibited the growth of Staphy-lococcus aureus (S. aureus) and Escherichia coli (E. coli).

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