Biosynthesized Ag nanoparticles on urea-based periodic mesoporous organosilica enhance galegine content in Galega.

The biological approach for synthesizing nanoparticles (NPs) using plant extracts is an efficient alternative to conventional physicochemical methods. Galegine, isolated from Galega (Galega officinalis L.), has anti-diabetic properties. In the present study, silver nanoparticles (AgNPs) loaded onto urea-based periodic mesoporous organosilica (AgNPs/Ur-PMO) were bio-synthesized using G. officinalis leaf extract. The synthesized NPs were characterized and confirmed via analysis methods. Different concentrations of biosynthesized AgNPs/Ur-PMO nanoparticles (0, 1, 5, 10, and 20 mg L-1) were used as elicitors in cell suspension culture (CSC) of G. officinalis. The callus cells from hypocotyl explants were treated at their logarithmic growth phase (8th d) and were collected at time intervals of 24, 72, 120, and 168 h. The viability and growth of cells were reduced (by 17% and 35%, respectively) at higher concentrations and longer treatments of AgNPs/Ur-PMO; however, the contents of hydrogen peroxide (H2O2) and malondialdehyde (MDA) were increased (1.23 and 3.01 fold, respectively in comparison with the control average). The highest total phenolic (2.43 mg g-1 dry weight) and flavonoid (2.22 mg g-1 dry weight) contents were obtained 168 h after treatment with 10 mg L-1 AgNPs/Ur-PMO. An increasing tendency in the antioxidant enzyme activities was also observed in all the elicitor concentrations. Treatment with AgNPs/Ur-PMO (in particular 5 mg L-1 for 120 h) significantly enhanced the galegine content (up to 17.42 mg g-1) about 1.80 fold compared with the control. The results suggest that AgNPs/Ur-PMO can be used as an effective elicitor for enhancing galegine production in the CSC of G. officinalis. KEY POINTS: • The green biosynthesis of AgNPs/Ur-PMO was done using G. officinalis leaf extract • Its toxicity as an elicitor increased with increasing concentration and treatment time • AgNPs/Ur-PMO significantly increased the antioxidant capacity and galegine content.

Nano-architecture of MOF (ZIF-67)-based Co3O4 NPs@N-doped porous carbon polyhedral nanocomposites for oxidative degradation of antibiotic sulfamethoxazole from wastewater.

Co3O4 NPs in N-doped porous carbon (Co3O4 NPs@N-PC) materials were prepared by one-pot pyrolysis of a ZIF-67 powder under N2 atmosphere and followed by oxidation under air atmosphere (200 °C) toward promotion catalytic activity and activation of peroxymonosulfate (PMS) to degradation sulfamethoxazole (SMZ). 2-methylimidazole was used as a nitrogen source and a competitive ligand for the synthesis of Co3O4 NPs@N-PC, which in addition to affecting nucleation and growth of the crystal, promotes the production of active Co-N sites. Co3O4 NPs@N-PC nano-architecture has high specific surface areas (250 m2 g-1) and is a non-toxic, effective and stable PMS activator. The effect of operating parameters including SMZ concentration, catalyst dosage, temperature and pH in the presence of Co3O4 NPs@N-PC was investigated. The Co3O4 NPs@N-PC composite showed superior performance in activating PMS over a wide range of pH (2-10) and different temperatures so that complete degradation of SMZ (50 µM, 100 mL) was achieved within 15 min. The role of Co2+/Co3+ redox system in the mechanism before and after PMS activation was determined using XPS analysis. Surface-generated radicals led to the degradation of SMZ, in which the SMZ degradation rate attained 0.21 min-1 with the mineralization of 36.8%. The feasible degradation mechanism of SMZ was studied in the presence of different scavengers and it was revealed that the degradation reaction proceeds from the radical/non-radical pathway and in this process most of the SO4- and OH radicals are dominant. The recoverability and reuse of Co3O4 NPs@N-PC were evaluated to confirm its stability and potential for SMZ degradation and it was observed that the catalyst maintains its catalytic power for at least 5 cycles.

Integration of plasmonic AgPd alloy nanoparticles with single-layer graphitic carbon nitride as Mott-Schottky junction toward photo-promoted H2 evolution.

Plasmonic AgPd alloy nanoparticles (AgPdNPs) decorated on single-layer carbon nitride (AgPdNPs/SLCN) for the designing of the Mott-Schottky junction were constructed with the ultrasonically assisted hydrothermal method and used toward photo evolution H2 from formic acid (FA) at near room temperature (30 °C). The Pd atom contains active sites that are synergistically boosted by the localized surface plasmon resonance (LSPR) effect of Ag atoms, leading to considerably enhanced photocatalytic properties. The photoactive AgPdNPs/SLCN obtained supreme catalytic activity to produce 50 mL of gas (H2 + CO2) with the initial turnover frequency of 224 h-1 under light irradiation. The catalyst showed stable catalytic performance during successive cycles.

Single-pot tandem oxidative/C-H modification amidation process using ultrasmall PdNP-encapsulated porous organosilica nanotubes.

Herein, we studied a single-pot method with a dual catalysis process towards the conversion of primary aromatic alcohols to amides using ultrasmall PdNPs of controlled uniform size (1.8 nm) inside hybrid mesoporous organosilica nanotubes (MO-NTs). The catalyst exhibited excellent performance in water under mild conditions and showed high stability. The catalytic activity towards the tandem oxidation of alcohols in the presence of amine salts and H2O2 to their corresponding amides without producing byproducts was evaluated, and high yields were obtained for all products. The structure of the organosilica nanotubes containing palladium nanoparticles was investigated using various characterization techniques such as XRD, TEM, BET, solid-state 29Si NMR and solid-state 13C CP MAS NMR. Catalyst recycling tests showed that the catalytic power of PdNPs@B-SNTs was preserved after 8 cycles and a slight decrease in catalyst activity was observed.

Biosynthesis of AgNPs onto the urea-based periodic mesoporous organosilica (AgxNPs/Ur-PMO) for antibacterial and cell viability assay.

Nano-size silver particles were stabilized on the inner surfaces of urea based periodic mesoporous organosilica (Ur-PMO). Aqueous extract of Euphorbia leaves as a sustainable and green reducing agent was applied for Ag-nanoparticles growth into the Ur-PMO channels. Physical and chemical properties of organosilica materials synthesized using various techniques such as FT-IR, small-angle XRD, PXRD, FESEM, TEM, SEM-EDX and atomic absorption spectrometry (AAS) were examined. Finally, the AgNPs/Ur-PMO were investigated on cell viability assay. An in vitro cytotoxicity test using MMT assay displayed that the designed material has good biocompatibility and could be a promising candidate for biomedical applications. The results also showed that the AgNPs/Ur-PMO compounds (especially, PMO; 1.27% AgNPs) had relatively good antibacterial and antibiofilm effects. It seems that the use of these compounds in hospital environments can reduce nosocomial infections as well as reduce antibiotic-resistant bacteria.

NH2-coordinately immobilized tris(8-quinolinolato)iron onto the silica coated magnetite nanoparticle: Fe3O4@SiO2-FeQ3 as a selective Fenton-like catalyst for clean oxidation of sulfides.

A green, robust and eco-friendly procedure for the oxidation of aromatic organic sulfides to sulfones using H2O2 catalyzed by NH2-coordinately immobilized tris(8-quinolinolato)iron onto the silica coated magnetite (Fe3SiO6) has been developed. Physicochemical properties of the resulting nanoparticles were investigated by means of techniques including X-ray diffraction, scanning electron microscopy, thermogravimetric analysis, vibrating sample magnetometer, atomic adsorption spectroscopy and FT-IR spectroscopy. The catalytic activity of sulfides oxidation showed that this atom-economical protocol provided great yields of various sulfones and allowed the sulfide function reaction conducting under the mild conditions thus to prevent the sulfide being over-oxidized to sulfoxides. The Fe3O4@SiO2-FeQ3 catalysts are magnetically separable and kept stable after recycling for 7 consecutive runs without detectable activity loss.