In this study, a simple and green method to synthesize silver nanoparticles (Ag NPs) in aqueous solution via ultrasonic irradiation has been developed. Ultrafine Ag NPs with average diameter of 8 nm were obtained through sonicating aqueous solution of sodium hydroxide (NaOH, 0.1 mM) with adding silver nitrate solution (AgNO3, 5.88 mM) drop by drop. In pure aqueous solution, the reactive route related to hydroxyl radicals (OH) is presented. Furthermore, in alkaline aqueous solution, the effects of hydroxyl ions (OH(-)) on formation of Ag NPs are discussed detailedly. The formation of Ag NPs was tracked by surface plasmon resonance (SPR) band of ultraviolet-visible (UV-Vis) spectrum; the morphology of the obtained Ag NPs was characterized through transmission electron microscopy (TEM); energy dispersive X-ray spectroscopy (EDX) and X-ray powder diffraction (XRD) confirmed the formation of metallic Ag NPs.
All-cis-1,2,3,4-tetrafluorocyclopentane is synthesised and experiment and theory data reveal a very highly polar aliphatic with Janus like electropositive and electronegative faces.
This paper describes the synthesis of a series of organic liquid crystals (LCs) containing selectively fluorinated cyclopropanes at their termini. The syntheses used difluorocarbene additions to olefin precursors, an approach which proved straightforward such that these liquid crystal candidates could be efficiently prepared. Their physical and thermodynamic properties were evaluated and depending on individual structures, they either displayed positive or negative dielectric anisotropy. The study gives some guidance into effective structure–property relationships for the design of LCs containing selectively fluorinated cyclopropane motifs.
An efficient cascade bicyclization strategy for the construction of γ-lactam containing 3,3-disubstituted oxindole derivatives under silver catalysis is described. The method enables the sequential assembly of both unactivated and activated...
A AgSCF3-mediated tandem trifluoromethylthiolaton and cyclization of N-aryl-3-butenamides was developed. It showed divergent reactivities and enabled the selective syntheses of CF3S-substituted 3,4-dihydroquinolin-2-ones and azaspiro[4,5]dienones. The selectivity was achieved through different...
A convenient copper-catalyzed cascade cyclization/cyanation reaction for the construction of cyano-containing γ-lactams was developed. The protocol employed TMSCN as the cyano source and proceeded in water under simple conditions. Mechanistic...
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