A rapid green approach for synthesizing of silver nanoparticles using Alpinia katsumadai seed extract is described and their antioxidant, antibacterial and cytotoxicity activities evaluated.

Although pyridine derivatives are versatile supporting ligands in catalysis, the development of their chiral versions has been relatively limited. Herein, we report the design, synthesis, and proof-of-concept application of a structurally tunable chiral pyridine framework featuring an annulated compact ring system. Using an N,B-bidentate ligand skeleton containing the chiral pyridine moiety, we have developed an enantioselective iridium-catalyzed desymmetrizing C–H borylation reaction of diaryl­(2-pyridyl)­methane compounds with up to 96% ee and 93% yield. The resulting borylation products could be readily transformed into various chiral tri­(hetero)­arylmethane compounds. Density functional theory investigations revealed that the two chair conformations of the flexible ketal motif both favored the enantiomer that was consistent with experimental results. This work has thus introduced an effective and tunable chiral pyridine ligand framework that may be used in many catalytic asymmetric transformations.

A simple approach using Nelumbo nucifera seeds for synthesizing silver nanoparticles with potential antibacterial and cytotoxic activities was described.

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A novel MoS2 piezoelectric nanocatalyst with multiple flaws exhibited ultrafast degradation of the antibiotic ciprofloxacin.