SYNTHESIS AND STRUCTURE OF IRON(III) COMPLEX WITH 2-ACETYLPYRIDINE-AMINOGUANIDINE

Schiff bases represent an interesting class of compounds due to a wide range of possible applications, especially their biological activity. Having in mind that the biological activity of the ligand could be closely related to its coordinating properties, we examined the synthesis and structure of a novel Fe(III) complex with the Schiff base of aminoguanidine and 2-acetylpyridine. Bis(ligand) complex of iron(III), of the formula [Fe(L–H)2]2(NCS)Cl, was obtained by the reaction of FeCl3 and the thiocyanate ligand salt in a mole ratio 1:1 in the presence of lithium-acetate as a deprotonating agent. The complex is obtained in the form of brown single crystals and is characterized by elemental analysis data, conductometric measurements, IR spectra, and X-ray analysis. The latter revealed that the chelating ligand is coordinated in its monoanionic form via pyridine, azomethine, and nitrogen atoms of the aminoguanidine fragment, forming octahedral environment.

Physicochemical and Electrochemical Characterization of Salt-in-Water and Water-in-Salt Potassium and Lithium Acetate Electrolytes

We report the physicochemical and electrochemical properties of various concentrations of potassium and lithium acetate (OAc) electrolytes from dilute to near saturation as well as mixed potassium/lithium acetate (32 m...

Niobium Tungsten Oxide in a Green Water-in-Salt Electrolyte Enables Ultra-Stable Aqueous Lithium-Ion Capacitors

Aqueous hybrid supercapacitors are attracting increasing attention due to their potential low cost, high safety and eco-friendliness. However, the narrow operating potential window of aqueous electrolyte and the lack of suitable negative electrode materials seriously hinder its future applications. Here, we explore high concentrated lithium acetate with high ionic conductivity of 65.5 mS cm−1 as a green “water-in-salt” electrolyte, providing wide voltage window up to 2.8 V. It facilitates the reversible function of niobium tungsten oxide, Nb18W16O93, that otherwise only operations in organic electrolytes previously. The Nb18W16O93 with lithium-ion intercalation pseudocapacitive behavior exhibits excellent rate performance, high areal capacity, and ultra-long cycling stability. An aqueous lithium-ion hybrid capacitor is developed by using Nb18W16O93 as negative electrode combined with graphene as positive electrode in lithium acetate-based “water-in-salt” electrolyte, delivering a high energy density of 41.9 W kg−1, high power density of 20,000 W kg−1 and unexceptionable stability of 50,000 cycles.

Mechanistic insights into the acetate-accelerated synthesis of crystalline ceria nanoparticles

Lithium acetate was reported to accelerate the growth of crystalline ceria nanoparticles in ozone-mediated synthesis through promoting alcohol-like condensation reactions.

Development of a Transformation Method for Metschnikowia borealis and other CUG-Serine Yeasts

Yeasts belonging to the Metschnikowia genus are particularly interesting for the unusual formation of only two needle-shaped ascospores during their mating cycle. Presently, the meiotic process that can lead to only two spores from a diploid zygote is poorly understood. The expression of fluorescent nuclear proteins should allow the meiotic process to be visualized in vivo; however, no large-spored species of Metschnikowia has ever been transformed. Accordingly, we aimed to develop a transformation method for Metschnikowia borealis, a particularly large-spored species of Metschnikowia, with the goal of enabling the genetic manipulations required to study biological processes in detail. Genetic analyses confirmed that M. borealis, and many other Metschnikowia species, are CUG-Ser yeasts. Codon-optimized selectable markers lacking CUG codons were used to successfully transform M. borealis by electroporation and lithium acetate, and transformants appeared to be the result of random integration. Mating experiments confirmed that transformed-strains were capable of generating large asci and undergoing recombination. Finally, random integration was used to transform an additional 21 yeast strains, and all attempts successfully generated transformants. The results provide a simple method to transform many yeasts from an array of different clades and can be used to study or develop many species for various applications.

Development of a Transformation Method for Metschnikowia borealis and Other CUG-Serine Yeasts

Yeasts belonging to the Metschnikowia genus are particularly interesting for the unusual formation of only two needle-shaped ascospores during their mating cycle. Presently, the meiotic process that can lead to only two spores from a diploid zygote is poorly understood. The expression of fluorescent nuclear proteins should allow the meiotic process to be visualized in vivo; however, no large-spored species of Metschnikowia has ever been transformed. Accordingly, we aimed to develop a transformation method for Metschnikowia borealis, a particularly large-spored species of Metschnikowia, with the goal of enabling the genetic manipulations required to study biological processes in detail. Genetic analyses confirmed that M. borealis, and many other Metchnikowiacea, are CUG-Ser yeasts. Codon-optimized selectable markers lacking CUG codons were used to successfully transform M. borealis by electroporation and lithium acetate, and transformants appeared to be the result of random integration. Mating experiments confirmed that transformed-strains were capable of generating large asci and undergoing recombination. Finally, random integration was used to transform an additional 18 yeast strains, and all attempts successfully generated transformants. The results provide a simple method to transform many yeasts from an array of different clades and can be used to study or develop many species for various applications.