Reduction Of Nitroarenes Research Articles

N, P co-doped coffee biochar-supported Ni-Nx for chemoselective reduction or reductive amination of nitroarenes using formic acid

In this study, we report an efficient, stable, and renewable N, P co-doped coffee biochar-based catalyst loaded with highly dispersed Ni-Nx species (Ni/NPCB-600), and it was successfully applied to the aqueous-phase chemoselective reduction or reductive amination of diverse nitroarenes (Yield up to >91%). Experimental and characterization studies revealed that N, P co-doping have a synergistic effect on improving the catalytic performance of Ni/NPCB-600. The textural properties of Ni/NPCB-600 are enhanced after doping of P, which can facilitate mass transfer and expose more accessible active sites in the reaction. The doping of N could induce the formation of Ni-Nx sites and enhance the basicity of the Ni/NPCB-600 catalyst, which can promote the adsorption and activation of formic acid and nitroarenes, respectively. This is the first example of N, P co-doped coffee biochar-based catalyst for nitroarenes reduction or reductive amination, and reveals its potential industrial application prospects.

Comparison of Ru(II)‒arene complexes containing naphthyl-/quinolinyl-substituted ligand vis-a-vis structure, spectra and catalytic activity

A series of ligands with naphthyl/quinolinyl substituent in their principal molecular framework were synthesised. Their corresponding half-sandwich ruthenium (Ru) complexes (Ru1a-b, Ru2a-b and Ru3) were then successfully generated. The structure of all synthesised compounds was comprehensively elucidated via 1H and 13C nuclear magnetic resonance (NMR), elemental analysis and Fourier-transform infrared spectroscopies. Notably, the structural configuration of Ru3 was delineated via X-ray diffraction. The catalytic efficacy of the Ru complexes was systematically probed in two distinct reactions: 1) transfer hydrogenation (TH) of ketones using 2-propanol as the hydrogen source and 2) reduction of nitroarenes to anilines using sodium tetrahydridoborate as the reducing agent in ethanol, conducted at ambient temperature. Comparative analysis of catalytic yields of the Ru complexes (Ru1a-b, Ru2a-b and Ru3) in both reaction types revealed that Ru3 delivered superior catalytic performance in both types of reactions. Furthermore, scrutiny of the 1H NMR spectrum during the TH reaction revealed formation of Ru-hydride species.

Catalytic Performance in Nitroarene Reduction of Nanocatalyst Based on Noble Metal Nanoparticles Supported on Polymer/s-Layer Protein Hybrids.

We present a novel bionanocatalyst fabricated by the adsorption-reduction of metal ions on a polyurethane/S-layer protein biotemplate. The bioinspired support was obtained by the adsorption of S-layer proteins (isolated from Lentilactobacillus kefiri) on polyurethane particles. Silver and platinum nanoparticles were well-loaded on the surface of the support after the combination with metallic salts and reduction with H2 at room temperature. Transmission electron microscopy analysis revealed the strawberry-like morphology of the bionanocatalysts with a particle size, dn, of 2.39 nm for platinum and 9.60 nm for silver. Both systems catalyzed the hydrogenation of p-nitrophenol to p-aminophenol with high efficiency in water at mild conditions in the presence of NaBH4. Three different amounts of bionanocatalyst were tested, and in all cases, conversions between 97 and 99% were observed. The catalysts displayed excellent recyclability over ten cycles, and no extensive damage in their nanostructure was noted after them. The bionanocatalysts were stable during their production, storage, and use, thanks to the fact that the biosupport provides an effective driving force in the formation and stabilization of the metallic nanoparticles. The successful bioinspired production strategy and the good catalytic ability of the systems are encouraging in the search for nontoxic, simple, clean, and eco-friendly procedures for the synthesis and exploitation of nanostructures.

AuNP/MIL-88B-NH2 Nanocomposite for the Valorization of Nitroarene by Green Catalytic Hydrogenation.

The efficiency of a catalytic process is assessed based on conversion, yield, and time effectiveness. However, these parameters are insufficient for evaluating environmentally sustainable research. As the world is urged to shift towards green catalysis, additional factors such as reaction media, raw material availability, sustainability, waste minimization and catalyst biosafety, need to be considered to accurately determine the efficacy and sustainability of the process. By combining the high porosity and versatility of metal organic frameworks (MOFs) and the activity of gold nanoparticles (AuNPs), efficient, cyclable and biosafe composite catalysts can be achieved. Thus, a composite based on AuNPs and the nanometric flexible porous iron(III) aminoterephthalate MIL-88B-NH2 was successfully synthesized and fully characterized. This nanocomposite was tested as catalyst in the reduction of nitroarenes, which were identified as anthropogenic water pollutants, reaching cyclable high conversion rates at short times for different nitroarenes. Both synthesis and catalytic reactions were performed using green conditions, and even further tested in a time-optimizing one-pot synthesis and catalysis experiment. The sustainability and environmental impact of the catalytic conditions were assessed by green metrics. Thus, this study provides an easily implementable synthesis, and efficient catalysis, while minimizing the environmental and health impact of the process.

Recent Advances in Catalytic Systems for the Reduction of Aromatic and Aliphatic Nitrile Compounds to Amines.

Amines are important and valuable compounds widely used in the chemical industry to produce various products such as dyes, detergents, solvents, additives, pharmaceutical products, and anti-foam agents. A property that distinguishes primary amines from other compounds is their straightforward functionalization. Therefore, the synthesis of different amine compounds has been considered by many researchers in recent years. Usually, primary amines are produced via amination of alcohols, reductive amination, and reduction of nitro and amide compounds. Furthermore, a useful and atom-economical method for producing primary amines is reducing nitrile compounds using catalytic systems. Traditionally, nitriles are reduced using metal hydrides such as LiAlH4 or NaBH4. These methods have important restrictions in terms of selectivity and waste generation. Hence, the heterogeneous and homogeneous catalysts were investigated for the hydrogenation of nitriles to diverse amines. This review describes the performance of different catalytic systems for reducing nitrile compounds to their corresponding amines.

Edge-site selective decoration of silver nanoparticles on TiO2 nanosheets for the rapid catalytic reduction of nitroarenes

In this study, we aim to construct an edge-site selective deposition of silver nanoparticles on TiO2 nanosheets (Ag-TiO2NSs) for the catalytic reduction of toxic nitroarenes (NAs) using NaBH4 medium. The as-prepared Ag-TiO2NSs were characterized by various analytical techniques such as XRD, HR-TEM, SEM-EDAX, elemental mapping and XPS analyses. The HR-TEM images confirmed that the Ag nanoparticles (AgNPs) size of around 3.05 ± 0.5 nm in diameter exhibited the selective growth specifically on the edges of the TiO2NSs. Additionally, it was observed that the TiO2NSs exhibited a high exposure of (101) facets. The prepared Ag-TiO2NSs catalyst exhibited remarkably high catalytic activity in the reduction of 4-nitrophenol (4-NP) (∼6 min, Kapp: 9.2 × 10−3 s−1 and TOF: 1.13 × 10−6 mol mg−1 min−1), which was comparable to or surpassing the catalytic performance of most of the previously reported Ag-based catalysts. Moreover, the catalyst showed an excellent catalytic reduction ability of other NAs such as 4-nitroaniline (4-NA) (∼10 min, 2.8 × 10−3 s−1), 4-(4-nitrophenyl)morpholine (4-NM) (∼8 min, 6.0 × 10−3 s−1), and 4-(2-fluoro-4-nitrophenyl)morpholine (4-FNM) (∼11 min, 4.2 × 10−3 s−1). In addition, the Ag-TiO2NSs exhibited commendable recyclability, with a minimal decrease in the activity over four consecutive recycling operations. The exceptional catalytic performance could be attributed to the smaller size of the AgNPs along with the synergistic effect between AgNPs and their interfacial contact with the (101) facet exposure of TiO2NSs. The Ag-TiO2NSs catalyst demonstrated the potential application for the catalytic reduction of 4-NP in a fixed bed reactor, operating under mild reaction conditions.

Formation of potentially toxic metabolites of drugs in reactions catalyzed by human drug-metabolizing enzymes.

Data are presented on the formation of potentially toxic metabolites of drugs that are substrates of human drug metabolizing enzymes. The tabular data lists the formation of potentially toxic/reactive products. The data were obtained from in vitro experiments and showed that the oxidative reactions predominate (with 96% of the total potential toxication reactions). Reductive reactions (e.g., reduction of nitro to amino group and reductive dehalogenation) participate to the extent of 4%. Of the enzymes, cytochrome P450 (P450, CYP) enzymes catalyzed 72% of the reactions, myeloperoxidase (MPO) 7%, flavin-containing monooxygenase (FMO) 3%, aldehyde oxidase (AOX) 4%, sulfotransferase (SULT) 5%, and a group of minor participating enzymes to the extent of 9%. Within the P450 Superfamily, P450 Subfamily 3A (P450 3A4 and 3A5) participates to the extent of 27% and the Subfamily 2C (P450 2C9 and P450 2C19) to the extent of 16%, together catalyzing 43% of the reactions, followed by P450 Subfamily 1A (P450 1A1 and P450 1A2) with 15%. The P450 2D6 enzyme participated in an extent of 8%, P450 2E1 in 10%, and P450 2B6 in 6% of the reactions. All other enzymes participate to the extent of 14%. The data show that, of the human enzymes analyzed, P450 enzymes were dominant in catalyzing potential toxication reactions of drugs and their metabolites, with the major role assigned to the P450 Subfamily 3A and significant participation of the P450 Subfamilies 2C and 1A, plus the 2D6, 2E1 and 2B6 enzymes contributing. Selected examples of drugs that are activated or proposed to form toxic species are discussed.

Selective Partial Reduction of Nitroarenes to the Hydrazoarene Catalyzed by Amine‐Modified Ordered Mesoporous Silica Immobilized Ionic Liquid (OMSIIL) Stabilised RuNPs

AbstractRuthenium nanoparticles stabilised by an amine‐modified Ordered Mesoporous Silica Immobilized Ionic Liquid (OMSIIL) are efficient catalysts for the partial reduction of nitrobenzene to hydrazobenzene with 100 % selectivity as well as the complete reduction to aniline. High selectivity for the partial reduction of nitrobenzene to hydrazobenzene was obtained when the reaction was conducted in ethanol with 0.5 mol% catalyst and NaBH4 as the hydrogen donor whereas aniline was obtained as the sole product in water when dimethylamine borane (DMAB) was used as the hydrogen donor. Interestingly, while a range of electron poor nitroarenes were reduced to the corresponding hydrazoarene with high selectivities and good conversions, nitroarenes substituted with electron donating groups resulted in complete reduction to the aniline. Composition‐time profiles suggest that reductions conducted in ethanol with sodium borohydride occur via the condensation pathway while those conducted in water using dimethylamine borane as the hydrogen source may well go via the direct pathway. This is the first example of the selective reduction of nitrobenzene to hydrazobenzene using a ruthenium nanoparticle‐based catalyst and the initial TOF of 320 mol nitrobenzene converted mol Ru−1 h−1 for the partial reduction of nitrobenzene to hydrazobenzene is markedly higher than previous literature reports. A study of the catalyst performance as a function of the surface modification revealed that each component has a direct and dramatic effect on the efficacy as RuNPs stabilised by COK‐12 modified with imidazolium‐based ionic liquid and a primary amine gave the highest conversion while selective removal of either component or replacement of the primary amine with a tertiary amine resulted in a marked reduction in efficiency.

Dumbbell-shaped polymeric nanoparticles with one-side anchored Pd-clusters for efficient catalytic hydrogenation at biphasic interfaces

Pickering interfacial catalysts incorporated with amphiphilic architecture significantly expand the sustainability of green catalysis systems. In this work, we present precise and well-designed dumbbell-shaped Janus-structured polymeric nanoparticles with one-side anchored palladium clusters (DB-JPP-Pd) as Pickering interfacial catalyst for static hydrogenations. The large wettability difference of each lobe renders the prominent amphiphilicity of the dumbbell-shaped DB-JPP-Pd. The amphiphilic Janus catalyst displays excellent interfacial activity and extensively reduces the interfacial tension from 34.06 ± 0.13 to 20.54 ± 0.31 mN/m, promoting the formation of a more stable Pickering emulsion than that of the bulk PS-Pd catalyst, which can continuously provide a large interfacial area and shorten the molecular mass transfer distance during the reaction process. As a result, the DB-JPP-Pd catalyzed nitroarene reduction reaction exhibits a normalized reaction rate constant (knor) of 3.39 min−1⋅g−1⋅L under static conditions, which is 56.5 times higher than that of bulk PS-Pd. The constructed Pickering interfacial catalysis (PIC) system converts all the nitrobenzene into aniline within three minutes and possesses excellent selectivity in hydrogenations of different nitro aromatics. In addition, the emulsion catalytic system was conveniently recycled for ten consecutive runs. Hence, this unique amphiphilic dumbbell-shaped catalyst effectively develops an efficient static biphasic catalysis system.

Novel magnetic bimetallic AuCu catalyst for reduction of nitroarenes and degradation of organic dyes.

Herein, core-shell magnetic nanoparticles are modified with imidazolium-tagged phosphine and propylene glycol moieties and used for the stabilization of bimetallic AuCu nanoparticles. The structure and morphology of the prepared material are identified with SEM, TEM, XRD, XPS, atomic absorption spectroscopy, Fourier translation infrared spectroscopy, and a vibrating sample magnetometer. This hydrophilic magnetic bimetallic catalyst is applied in the reduction of toxic nitroarenes and reductive degradation of hazardous organic dyes such as methyl orange (MO), methyl red (MR), and rhodamine B (RhB), as well as in the degradation of tetracycline (TC). This magnetic AuCu catalyst indicated superior activity in all three mentioned reactions in comparison with its single metal Au and Cu analogs. This catalyst is recycled for 17 consecutive runs in the reduction of 4-nitrophenol to 4-aminophenol without a significant decrease in catalytic activity and recycled catalyst is characterized.

Metal-facilitated, sustainable nitroarene hydrogenation under ambient conditions

Hydrogenation is a critical reaction in the chemical industry, yielding a range of important compounds such as fine chemicals, pharmachemicals and agrochemicals. However, conventional hydrogenation typically requires pressurized hydrogen, high temperatures and involves noble metal catalysts. We proposed a two-step hydrogenation process, utilizing water as the hydrogen source for the industrially important reduction of nitroarenes to anilines. A metal or reduced metal oxide, which can be obtained from solar thermal or electrochemical reduction, acts as the active site for nitrobenzene adsorption, H2O dissociation and in-situ hydrogen generation. Among the 15 metal and reduced metal oxides investigated, Zn and Sn emerged as highly efficient catalysts for the reduction of a broad range of organic nitro compounds under mild conditions, with H2 utilization efficiency 1–2 orders of magnitude above the state-of-the-art. The presented protocol provides extra dimensions for designing and optimizing conventional hydrogenation process with an alternative pathway. The reactive hydrogen atoms generated in-situ effectively overcome the barriers associated with hydrogen gas dissolution and its subsequent dissociation on the catalyst surface, thereby greatly enhancing the overall effectiveness for the hydrogenation reaction. This research potentially establishes a sustainable, generally applicable alternative to conventional hydrogenation methods, simultaneously presenting a viable solution for renewable energy storage.

Design and synthesis of chitosan/calcium lignosulfonate/Au NPs: Its performance for reduction of nitro compounds and in the treatment of cancer

This work introduces the preparation of a novel type of crosslinked polymers support based on calcium lignosulfonate-chitosan (CLS-CS) hydrogel with capping/reducing ability to encapsulated gold nanoparticles (CLS-CS/Au NPs). The morphology, structure and physicochemical properties of the prepared nanoparticles were characterized by different analytical techniques such as FT-IR, FE-SEM, TEM, EDX-elemental mapping study. The obtained results shown that CLS-CS/Au NPs prepared as spherical particles with sizes of 20–30 nm. The CLS-CS/Au NPs was applied as well for reduction of nitroarenes. The reduction of nitroarenes was obtained with good to high yields within short times. The related nanocatalyst was recovered for eight runs without significant loss of its catalytic performance. The MTT examination was conducted to check the anti-pancreatic cancer, anti-gastric cancer, anti-colorectal carcinoma, and cytotoxicity efficacies of the treated cells with CLS-CS/Au NPs over a 48-hour period on normal (HUVEC) and cancer cells. The IC50 values of the CLS-CS/Au NPs were found to be 169 µg/mL for HT-29 (colorectal carcinoma cell), 196 µg/mL for MKN45 (Gastric cancer cell), and 112 µg/mL for PANC-1 (Pancreatic cancer cell). The growth of malignant colorectal, gastric and pancreatic cells was found to decrease in a dose-dependent manner when exposed to CLS-CS/Au NPs. Following clinical research, CLS-CS/Au NPs shows promise as an effective treatment for colorectal, gastric and pancreatic cancers.

Harnessing the Oxygen Vacancies in Metal Oxides for Nitroreduction

AbstractOxygen vacancies are one of the prominent types of defects in metal oxides. In addition to their role in modifying the electronic properties in solids, these sites have been shown to activate chemical bonds. As a result, the use of defect‐rich metal oxides in the organic transformations is promising. The article gives an overview of various chemical processes that are in use for the chemical reduction of aromatic nitro compounds to amines. Recently, application of oxygen vacancies in transition metal oxide for the selective reduction of aromatic nitro compounds to the corresponding amines has emerged as a new method of synthesis of amines. Oxygen vacancies in reducible oxide such as CuO have been shown to decompose hydrazine hydrate to H2 and in situ cause the reduction of nitro arenes to corresponding amines. This concept article discusses the literature pertaining to the synthesis of nitro reduction reaction, various strategies employed thus far and the place the defect‐mediated synthesis holds. The article also discusses the perspectives and challenges that remain to be addressed to gain more insights into the mechanistic understanding of the role of oxygen vacancies in nitro reduction and beyond.

Unraveling discriminative-hydrogen-activation over Cu-based catalysts for boosting nitroarenes hydrogenation: Crystal effect and mechanism insight

Copper is a crucial element in the field of catalysis. However, Cu-based catalysts exhibit lower redox properties and surface energy under mild conditions, which limit their electron transfer capacities and catalytic performance. In this study, the relationship investigation between the hydrogenation behavior of Cu-based catalysts and crystal phases showed that spherical Cu2O exhibited enhanced capacity for hydrogen activation, excellent catalytic activity and outstanding reusability in the selective reduction of various nitroarenes. At even 25 °C and 1 atm, the complete reduction of 4-nitrophenol by NaBH4 was achieved in 2.5 min over Cu2O, achieving a reaction rate constant (k) of 20.15 × 10−3 s−1, which was 4.8 and 15.2 times that of CuO and Cu catalysts. Detailed experimental and theoretical calculations revealed that the Cu+ sites in the antifluorite crystal phase of Cu2O are conducive to the adsorption of active H species, while the unique d–s orbital recombination provides more electrons to improve its hydrogenation performance. The results of this study can aid in the development of copper-based materials as advanced catalysts, thereby improving fine chemical production and pollution treatment processes.

Liquid-Liquid interfacial approach for rapid synthesis of Well-Crystalline Two-Dimensional Metal-Organic frameworks for nitro reduction

Two-dimensional metal–organic frameworks (2D MOFs) have garnered significant attention due to their exceptional properties across diverse research domains, including catalysis, biomedicine, gas adsorption, separation, energy storage, and sensing. Despite these promising attributes, the facile and large-scale synthesis of 2D MOFs with high crystallinity remains a formidable challenge. In this study, we propose a novel approach based on a modified liquid–liquid interfacial method for the rapid synthesis of well-crystalline 2D MOFs. By vigorously mixing water, a hydrophobic solvent, and an emulsifier, we generate micrometer-sized droplets that create substantial curved two-phase interfaces. This method is compatible with various ligands and metal ions, enabling the rapid formation of 2D MOFs at these curved interfaces under additional pressure. The subsequent separation of oil and water phases via centrifugal force promotes moderate π-π stacking within the 2D MOF, thereby stabilizing the lamellar structure and enriching the material at the two-phase interface. Remarkably, the entire synthesis process requires a mere 3 min, yielding grams of product in a single run. Furthermore, solvent reuse does not compromise the quality of the resulting 2D MOFs. As a practical application, we synthesized phthalocyanine (Pc)-based structures using this method for the catalytic reduction of nitroaromatics. Among these, Cu-CoPc (2D MOFs with Cu2+ coordinated to CoPc) emerged as the most active catalyst, achieving a turnover frequency (TOF) value of 4726 h−1 for the reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP). Notably, this TOF value surpasses that of non-precious catalysts and is 180 times higher than that of commercial Pd/C (10 wt%).

Graphene quantum dots incorporated ZIF‐67 for stabilization of Au nanoparticles: Efficient catalyst for A3‐coupling and nitroarenes reduction reactions

Zeolitic imidazolate framework‐67 (ZIF‐67) functionalized with graphene quantum dots was prepared and utilized for the reduction of Au (III) and stabilization of Au nanoparticles. This newly prepared ZIF‐67/GQD@Au was characterized with different techniques and employed as a capable heterogeneous catalyst for reduction of aromatic nitro compounds and A1‐coupling reaction of alkynes, amines, and aldehydes in water solvent. Experiments indicate that this catalyst is able to reduce nitroarenes in short reaction times (10–20 min) in water at room temperature and corresponding amines were obtained in excellent yields (90–100%). Also, reactions of structurally different alkynes, amines, and aldehydes in the presence of this catalyst proceed effectively at 60°C and desired propargylic amine achieved in good to very good yields (76–88%) in water during 1 day. This catalyst displayed excellent stability and recyclability in both reactions and recycled for six runs with a small decrease in the activity.

Reduction-Specified Coupling Reactions of Nitroarenes by Heterogeneous Cobalt Catalysis.

The in-depth study on reduction-specified coupling reactions of the nitroarenes by heterogeneous cobalt catalysis opens a door for diversified syntheses of functional N-containing molecules. Guided by the structure-function relationship of heterogeneous materials, rational design of nano-catalysts can effectively regulate the routes of organic reactions. Precise transformation of the intermediates generated during the nitroarene reduction with a suitable nano-catalyst is a promising way to develop new tandem reactions, and to synthesize structurally novel compounds that are of difficult access with the conventional approaches.

Zn/Al layered double hydroxide and carboxymethyl cellulose composite beads as support for the catalytic gold nanoparticles and their applications in the reduction of nitroarenes

Until now, many efficient catalysts have been reported that are used for the reduction of nitroarenes. However, a catalyst reusability is a challenge that is often faced in practical environment. In this report, we designed a hydrogel composite (CMC-LDH), which act as support and making it possible to address this challenge. In this research work, zinc/aluminum based layered double hydroxides (Zn/Al LDH) have been assembled with carboxymethyl cellulose (CMC) to prepare CMC/LDH hydrogel beads. The CMC/LDH hydrogel beads were prepared by the ionotropic gelation method. For CMC/LDH/Au preparation, the already prepared CMC/LDH beads were kept in gold ion (Au3+) solution, and their subsequent reduction with sodium borohydride (NaBH4). For the characterization of the prepared samples different instrumental techniques, such as Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy, and scanning electron microscopy (SEM) were adopted. For the catalytic evaluation of CMC/LDH/Au, it was utilized as a catalyst in 4-NP and 4-NA reduction reactions. The continuity of the reaction was monitored by a UV–visible spectrophotometer. Rate constant (kapp) of 0.48474 min−1 and 0.7486 min−1 were obtained for 4-NP and 4-NA reduction, respectively. The hydrogel beads were recycled and reused for up to five successive cycles without significantly changing their catalytic efficiency.

White LED light mediated green photoreduction of nitroarenes to anilines on bimetallic Ni/Ag@resin: In situ SERS monitoring and evaluation of plasmonic effect

Reduction of nitroarenes to anilines, a potentially important organic transformation, is classically performed in harsh conditions, which have long lasting safety issues and wastage of energy. Herein, we report an efficient hot-electron induced reduction of nitroarenes to the corresponding anilines over bimetallic Ni/Ag@resin in presence of NaBH4 under white LED light irradiation. Mechanistically, the hot electrons assisted the dimerization of 4-NTP to cis-4,4′-dimercaptoazobenzene as the active intermediate evidenced by appearance of SERS peaks at 1389 cm−1. Hot electrons having energy content above a threshold can transfer the energy effectively to the LUMOs of the reactant nitroarenes. Overall the present catalyst system constitutes one straightforward and environmentally safe approach to a class of much sought organic transformation.

Bimetallic nanoparticles supported on Ce-BTC for highly efficient and stable reduction of nitroarenes: Towards environmental sustainability

The development of a catalyst with a consistent and clearly defined crystal structure is crucial for establishing an efficient catalytic performance system. This study focuses on catalyzing the reduction of nitroarenes to amino-derivatives in an aquatic environment at ambient temperature, employing metallic (Au) and bimetallic (Au–Pd or Au–Ag) nanoparticles loaded on a Ce-BTC metal–organic framework using a facile sol-immobilization approach. Diverse analytical instruments, comprising SEM, TEM, XRD, FT-IR, XPS, TGA, and N2 isotherm, have been utilized to characterize the synthesized catalysts. Among the catalysts that were fabricated, Au–Pd@Ce-BTC displayed the maximum catalytic efficacy, offering a rate constant (kapp) of 0.5841 min−1, conversion percentages reaching 99.7%, and a KAF of 116.8 min−1g−1. Moreover, it exhibited remarkable recyclability over five consecutive cycles. This catalyst offers the advantages of operating under ambient reaction conditions and exhibiting tolerance to a broad range of substrates containing various functional moieties. The mechanistic understanding of nitroarene reduction and the factors contributing to the superior activity of Au–Pd/Ce-BTC are explored through spectroscopic and porosity analyses. Spectroscopic measurements indicate that the elevated Auo and Pdo/Pd2+ ratio, increased surface area, and the synergistic collaboration of the bimetallic NPs are key factors contributing to the heightened activity of Au–Pd/Ce-BTC. These findings hold significant appeal from both an industrial and academic standpoint.