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Palladium (Pd), a noble metal, has unique properties for C-C bond formation in reactions such as the Suzuki and Heck reactions. Besides Pd-based complexes, Pd NPs have also attracted significant attention for applications such as fuel cells, hydrogen storage, and sensors for gases such as H2 and non-enzymatic glucose, including catalysis. Additionally, Pd NPs are catalysts in environmental treatment to abstract organic and heavy-metal pollutants such as Cr (VI) by converting them to Cr(III). In terms of biological activity, Pd NPs were found to be active against Staphylococcus aureus and Escherichia coli, where 99.99% of bacteria were destroyed, while PVP-Pd NPs displayed anticancer activity against human breast cancer MCF7. Hence, in this review, we attempted to cover recent progress in the various applications of Pd NPs with emphasis on their application as sensors and catalysts for energy-related and other applications. [ABSTRACT FROM AUTHOR]

Hybrid materials based on metal-organic frameworks (MOFs) and nanoparticles (NPs) have gained considerable popularity in a variety of applications. Particularly, these types of materials have demonstrated excellent efficiency in heterogeneous catalysis due to the synergistic effect between the components. Herein, we report a simple, eco-friendly, photocatalytic method for the fabrication of Zr containing MOF-801 and a silver (Ag) NPs-based hybrid (Ag@MOF-801). In this method, the photocatalytic property of the central metal ion (Zr) of MOF was exploited to promote the formation and deposition of Ag NPs on the surface of the MOF-801 under the irradiation of visible light. The successful incorporation of Ag NPs was ascertained by powder X-ray diffraction (XRD) and UV-Vis analysis, while the morphology and surface area of the sample was determined by N2 adsorption–desorption and scanning electron microscopy (SEM), respectively. The resulting Ag@MOF-801 hybrid served as a highly efficient catalyst for the transesterification of used vegetable oil (UVO) for the production of biodiesel. The Ag@MOF-801 catalyst exhibited superior catalytic activity compared to its pristine MOF-801 counterpart due to the enhanced surface area of the material. [ABSTRACT FROM AUTHOR]

Dry reforming of methane (DRM) over an Ni-based catalyst is an innovative research area due to the growing environmental awareness about mitigating global warming gases (CH4 and CO2) and creating a greener route of synthesis. Herein, 5% Ni supported on ZrO2 obtained from various sources was prepared by the impregnation method. The catalysts were calcined at 600, 700, and 800 °C. Furthermore, Ni-RC stabilized with MgO, SiO2, TiO2, and Y2O3 were tested. Characterization techniques employed comprise the N2 physisorption, infrared spectroscopy, Raman, thermogravimetric analysis, XRD, and TEM. The results of the present study indicated that the ZrO2 support source had a profound effect on the overall performance of the process. The best catalyst Ni-RC gave an average conversion of CH4 and CO2 of 61.5% and 63.6% and the least deactivation of 10.3%. The calcination pretreatment differently influenced the catalyst performance. When the average methane conversion was higher than 40%, increasing the calcination temperature decreased the activity. While for the low activity catalysts with an average methane conversion of less than 40% the impact of the calcination temperature did not constantly decrease with the temperature rise. The stabilization of Ni-RC denoted the preference Y2O3 stabilized catalyst with average values of CH4 and CO2 conversion of about 67% and 72%, respectively. The thorough study and fine correlation will be advantageous for technologically suitable Ni-15Y-RC catalysts for DRM. [ABSTRACT FROM AUTHOR]

Nanocomposites of highly reduced graphene oxide (HRG) and ZnOx nanoparticles doped manganese carbonate containing different percentages of HRG were prepared via a facile co-precipitation method. The prepared sample calcined at 300 °C yielded i.e., ZnOx(1%)-MnCO3/(X%)HRG (where X = 0-7), calcination at 400 °C and 500 °C, yielded different manganese oxides i.e., ZnOx(1%)-MnO2/(X%)HRG and ZnOx(1%)-Mn2O3/(X%)HRG respectively. The prepared catalyst were subjected to catalytic evaluation and a comparative catalytic study between carbonates and oxides for the liquid-phase aerobic oxidation of benzylic alcohols to corresponding aldehydes using molecular oxygen as an eco-friendly oxidant without adding additives or bases. The influence of various parameters such as percentage of HRG, reaction time, catalyst amount, calcination and reaction temperature was systematically examined to optimize reaction conditions using oxidation of benzyl alcohol as a substrate model. It was found that the catalytic performance is remarkably enhanced after using HRG as catalyst co-dopant for the aerobic oxidation of alcohols, possibly owing to the presence of carbon defects and oxygenated functional groups on HRG surface. The as-synthesized catalysts were characterized by SEM, EDX, XRD, Raman, TGA, BET, and FT-IR. Under optimal conditions, the catalyst with composition ZnOx(1%)-MnCO3/(1%)HRG calcined at 300 °C exhibited remarkable specific activity (57.1 mmol·g-1·h-1) with 100% conversion of benzyl alcohol and more than 99% product selectivity within extremely short time (7 min). The as-prepared catalyst was re-used up to five consecutive times without significant decrease in its activity and selectivity. To the best of our knowledge, the achieved specific activity is the highest so far compared to the earlier reported catalysts used for the benzyl alcohol oxidation. A wide range of substituted benzylic and aliphatic alcohols were selectively oxidized into their corresponding aldehydes with complete convertibility and selectivity in short reaction times without over-oxidation to the acids. Due to their significant low cost, superior reproducibility, excellent catalytic efficiency, the ZnOx(1%)-MnCO3/(X%)HRG nanocomposites possess several application prospect in other organic chemistry reactions. [ABSTRACT FROM AUTHOR]

Suzuki-Miyaura coupling reaction catalyzed by the palladium (Pd)-based nanomaterials is one of the most versatile methods for the preparation of biaryls. However, use of organic solvents as reaction medium causes a big threat to environment due to the generation of toxic byproducts as waste during the work up of these reactions. Therefore, the use of water as reaction media has attracted tremendous attention due to its environmental, economic, and safety benefits. In this study, we report on the synthesis of green Pd@graphene nanocatalyst based on an in situ functionalization approach which exhibited excellent catalytic activity towards the Suzuki-Miyaura cross-coupling reactions of phenyl halides with phenyl boronic acids under facile conditions in water. The green and environmentally friendly synthesis of Pd@graphene nanocatalyst (PG-HRG-Pd) is carried out by simultaneous reduction of graphene oxide (GRO) and PdCl2 using Pulicaria glutinosa extract (PGE) as reducing and stabilizing agent. The phytomolecules present in the plant extract (PE) not only facilitated the reduction of PdCl2, but also helped to stabilize the surface of PG-HRG-Pd nanocatalyst, which significantly enhanced the dispersibility of nanocatalyst in water. The identification of PG-HRG-Pd was established by various spectroscopic and microscopic techniques, including, high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), ultraviolet-visible spectroscopy (UV-Vis), Fourier transform infrared spectroscopy (FT-IR), and Raman spectroscopy. The as-prepared PG-HRG-Pd nanocatalyst demonstrated excellent catalytic activity towards the Suzuki-Miyaura cross coupling reactions under aqueous, ligand free, and aerobic conditions. Apart from this the reusability of the catalyst was also evaluated and the catalyst yielded excellent results upon reuse for several times with marginal loss of its catalytic performance. Therefore, the method developed for the green synthesis of PG-HRG-Pd nanocatalyst and the eco-friendly protocol used for the Suzuki coupling offers a mild and effective substitute to the existing protocols and may significantly contribute to the endeavors of green chemistry. [ABSTRACT FROM AUTHOR]

The synthesis of 14-aryl 14H-dibenzo[a,j]xanthenes is achieved by a simple condensation reaction between β-naphthol with aryl or alkyl aldehydes in an effective synergetic catalytic system created by combining basic bleaching earth clay and PEG-600. The advantages of the present method include catalyst recyclability, superior product yield, a shorter reaction time and the avoidance of hazardous reagents. Synthesized xanthene derivatives were also screened for their antibacterial activity against Staphylococcus aureus (MTCC 96) and Pseudomonas aeruginosa (Wild). [ABSTRACT FROM AUTHOR]

Catalytic efficacy of metal-based catalysts can be significantly enhanced by doping graphene or its derivatives in the catalytic protocol. In continuation of previous work regarding the catalytic properties of highly-reduced graphene oxide (HRG), graphene-oxide (GO) doped mixed metal oxide-based nanocomposites, herein we report a simple, straightforward and solventless mechanochemical preparation of N-doped graphene (NDG)/mixed metal oxide-based nanocomposites of ZnO–MnCO3 (i.e., ZnO–MnCO3/(X%-NDG)), wherein N-doped graphene (NDG) is employed as a dopant. The nanocomposites were prepared by physical milling of separately fabricated NDG and ZnO–MnCO3 calcined at 300 °C through eco-friendly ball mill procedure. The as-obtained samples were characterized via X-ray diffraction (XRD), Thermogravimetric analysis (TGA), Fourier-transform infrared spectroscopy (FT-IR), Raman, Field emission scanning electron microscopy (FESEM), Energy-dispersive X-ray spectroscopy (EDX) and surface area analysis techniques. To explore the effectiveness of the obtained materials, liquid-phase dehydrogenation of benzyl alcohol (BOH) to benzaldehyde (BH) was chosen as a benchmark reaction using eco-friendly oxidant (O2) without adding any harmful surfactants or additives. During the systematic investigation of reaction, it was revealed that the ZnO–MnCO3/NDG catalyst exhibited very distinct specific-activity (80 mmol/h.g) with a 100% BOH conversion and <99% selectivity towards BH in a very short time. The mechanochemically synthesized NDG-based nanocomposite showed remarkable enhancement in the catalytic performance and increased surface area compared with the catalyst without graphene (i.e., ZnO–MnCO3). Under the optimum catalytic conditions, the catalyst successfully transformed various aromatic, heterocyclic, allylic, primary, secondary and aliphatic alcohols to their respective ketones and aldehydes with high selectively and convertibility without over-oxidation to acids. In addition, the ZnO–MnCO3/NDG was also recycled up to six times with no apparent loss in its efficacy. [ABSTRACT FROM AUTHOR]

Degradation of organic dyes and their byproducts by heterogeneous photocatalysts is an essential process, as these dyes can be potentially discharged in wastewater and threaten aquatic and xerophyte life. Therefore, their complete mineralization into nontoxic components (water and salt) is necessary through the process of heterogeneous photocatalysis. In this study, Zr/CrO2 (Zirconium-doped chromium IV oxide) nanocomposite-based photocatalysts with different compositions (1, 3, 5, 7 & 9 wt.%) were prepared by an environmentally friendly, solid-state reaction at room temperature. The as-prepared samples were calcined under air at 450 °C in a furnace for a specific period of time. The synthesis of Zr/CrO2 photocatalysts was confirmed by various techniques, including XRD, SEM, EDX, FT-IR, UV-Vis, and BET. The photocatalytic properties of all samples were tested towards the degradation of methylene blue and methyl orange organic dyes under UV light. The results revealed a concentration-dependent photocatalytic activity of photocatalysts, which increased the amount of dopant (up to 5 wt.%). However, the degradation efficiency of the catalysts decreased upon further increasing the amount of dopant due to the recombination of holes and photoexcited electrons. [ABSTRACT FROM AUTHOR]

In recent years, the development of green mechanochemical processes for the synthesis of new catalysts with higher catalytic efficacy and selectivity has received manifest interest. In continuation of our previous study, in which graphene oxide (GRO) and highly reduced graphene oxide (HRG) based nanocomposites were prepared and assessed, herein, we have explored a facile and solvent-less mechanochemical approach for the synthesis of N-doped graphene (NDG)/mixed metal oxide (MnCO3–ZrO2) ((X%)NDG/MnCO3–ZrO2), as the (X%)NDG/MnCO3–ZrO2 nano-composite was synthesized using physical grinding of separately synthesized NDG and pre-calcined (300 °C) MnCO3–ZrO2 via green milling method. The structures of the prepared materials were characterized in detail using X-ray powder diffraction (XRD), Field Emission Scanning Electron Microscope (FESEM), Energy Dispersive X-Ray Analysis (EDX), Fourier-transform infrared spectroscopy (FTIR), Raman, Thermogravimetric analysis (TGA), and N2 adsorption-desorption isotherm analysis. Besides, the obtained nanocomposites were employed as heterogeneous oxidation catalyst for the alcohol oxidation using green oxidant O2 without involving any surfactants or bases. The reaction factors were systematically studied during the oxidation of benzyl alcohol (PhCH2OH) as the model reactant to benzaldehyde (PhCHO). The NDG/MnCO3–ZrO2 exhibits premium specific activity (66.7 mmol·g−1·h−1) with 100% conversion of PhCH2OH and > 99.9% selectivity to PhCHO after only 6 min. The mechanochemically prepared NDG based nanocomposite exhibited notable improvement in the catalytic efficacy as well as the surface area compared to the pristine MnCO3–ZrO2. Under the optimal circumstances, the NDG/MnCO3–ZrO2 catalyst could selectively catalyze the aerobic oxidation of a broad array of alcohols to carbonyls with full convertibility without over-oxidized side products like acids. The NDG/MnCO3–ZrO2 catalyst were efficiently reused for six subsequent recycling reactions with a marginal decline in performance and selectivity. [ABSTRACT FROM AUTHOR]

Recently, the development of eco-friendly mechanochemical approaches for the preparation of novel catalysts with enhanced activity and selectivity has gained considerable attention. Herein, we developed a rapid and solvent-less mechanochemical method for the preparation of mixed metal oxide (Ag2O–MnO2) decorated graphene oxide (GRO)-based nanocomposites (Ag2O–MnO2/(X wt.%)GRO), as the Ag2O–MnO2/(X wt.%)GRO nanocomposite was fabricated by the physical grinding of freshly prepared GRO and pre-annealed (300 °C) mixed metal oxide nanoparticles (NPs) (Ag2O–MnO2) using an eco-friendly milling procedure. The as-prepared nanocatalysts were characterized by using various techniques. Furthermore, the nanocomposites were applied as a heterogeneous catalyst for the oxidation of alcohol by employing gaseous O2 as an eco-friendly oxidant under base-free conditions. The mechanochemically obtained GRO-based composite exhibited noticeable enhancement in the surface area and catalytic performance compared to the pristine Ag2O–MnO2. The results revealed that (1%)Ag2O–MnO2/(5 wt.%)GRO catalyst exhibited higher specific performance (13.3 mmol·g−1·h−1) with a 100% conversion of benzyl alcohol (BnOH) and >99% selectivity towards benzaldehyde (BnH) within 30 min. The enhancement of the activity and selectivity of GRO-based nanocatalyst was attributed to the presence of various oxygen-containing functional groups, a large number of defects, and a high specific surface area of GRO. In addition, the as-prepared nanocatalyst also demonstrated excellent catalytic activity towards the conversion of a variety of other alcohols to respective carbonyls under optimal conditions. Besides, the catalyst ((1%)Ag2O–MnO2/(5 wt.%)GRO) could be efficiently recycled six times with no noticeable loss in its performance and selectivity. [ABSTRACT FROM AUTHOR]

Graphene and its nanocomposites are showing excellent potential in improving the catalytic performances of different materials. However, the synthetic protocol and its form, such as graphene oxide (GRO) or highly reduced graphene oxide (HRG), influence the catalytic efficiencies. Here, we present, a facile synthesis of graphene oxide (GRO) and ZrOx-MnCO3-based nanocomposites [(1%)ZrOx–MnCO3/(x%)GRO] and their outcome as an oxidation catalyst for alcohol oxidation under mild conditions using O2 as a clean oxidant. The ZrOx–MnCO3/GRO catalyst prepared by incorporating GRO to pre-calcined ZrOx-MnCO3 using ball milling showed remarkable enhancement in the catalytic activities as compared to pristine ZrOx–MnCO3, ZrOx–MnCO3 supported on HRG or ZrOx–MnCO3/GRO prepared by in-situ growth of ZrOx–MnCO3 onto GRO followed by calcination. The catalyst with composition (1%)ZrOx–MnCO3/(1%)GRO exhibited superior specific activity (57.1 mmol/g·h) with complete conversion and >99% selectivity of the product within a short period of time (7 min) and at a relatively lower temperature (100 °C). The catalyst could be recycled at least five times with a negligible decrease in efficiency and selectivity. The catalytic study was extended to different aromatic as well as aliphatic alcohols under optimized conditions, which confirmed the efficiency and selectivity of the catalyst. [ABSTRACT FROM AUTHOR]

Nitrogen-doped graphene (NDG)-palladium (Pd)-based nanocatalysts (NDG@Pd) can be potentially applied as an efficient catalyst for the preparation of biaryls in a Suzuki–Miyaura coupling reaction. Herein, we report the one-pot facile synthesis of an NDG@Pd nanocatalyst, wherein the nanocatalyst was prepared by the simultaneous reduction of graphene oxide (GRO) and PdCl2 in the presence of hydrazine hydrate as a reducing agent, while ammonium hydroxide was used as a source of "N" on the surface of graphene. The as-synthesized NDG@Pd nanocatalyst, consisting of smaller-sized, spherical-shaped palladium nanoparticles (Pd-NPs) on the surface of NDG, was characterized by several spectroscopic and microscopic techniques, including high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), ultraviolet–visible spectroscopy (UV-Vis), Fourier-transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), and Brunauer–Emmett–Teller (BET). The nanocatalyst displayed outstanding catalytic activity in the Suzuki–Miyaura cross-coupling reactions of phenyl halides with phenyl boronic acids under facile conditions in water. The catalytic activity of NDG@Pd was found to be a more efficient catalyst when compared to pristine highly reduced graphene oxide (HRG) based Pd nanocatalyst (HRG@Pd). Furthermore, the reusability of the catalyst was also tested by repeatedly performing the same reaction using the recovered catalyst. The N-doped catalyst displayed excellent reusability even after several reactions. [ABSTRACT FROM AUTHOR]