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In the current report, we introduce a simple, mild efficient and green protocol for N-formylation and N-acetylation of anilines using formamide, formic acid, and acetic acid as inexpensive, nontoxic, and easily available starting materials just with heating along stirring in [ChCl][ZnCl2]2 as a durable, reusable deep eutectic solvent (DES), which acts as a dual catalyst and solvent system to produce a wide range of formanilides and acetanilides. Also, a variety of unsymmetrical urea derivatives were synthesized by the reaction of phenyl isocyanate with a range of amine compounds using this benign DES in high to excellent yields. [ChCl][ZnCl2]2 showed good recycling and reusability up to four runs without considerable loss of its catalytic activity. [ABSTRACT FROM AUTHOR]

In the presented work, a series of asymmetric dicationic ionic liquids (ADILs) with different alkyl chain length spacer between the two cation nuclei (imidazolium and pyridinium) with chlorine halide anion was designed, synthesized with excellent yield (89, 90 and 88%) and well characterized via different tools of analysis (FT-IR and 1H-NMR spectroscopy and thermal gravimetric analysis; TGA). The synthesized ADILs were examined for potential esterification as recyclable catalysts including the activity of catalytic performance, the reaction conditions justifying. The noted resulted data indicated that the butyric acid was converted perfectly into ester in presence of ADILs with short time of reaction. By completing our studies through the effect of chemical structures, concentrations, time and temperatures, we found that the synthesized Py-6-Imi exhibit the best catalytic performance with 96% as conversion value after 20 min at the ambient temperature (25 °C). The synthesized ADILs also recovered and reused for minimum three rounds without any significant reduction in the catalytic performance. Totally, the usage of ADILs in the esterification process offers lots of benefits such as perfect yield, quick time and environmentally friendly characteristics which make them the optimum sustainable compounds to be achieved in variety of industrial applications. [ABSTRACT FROM AUTHOR]

The aim of this work was to provide a novel approach to designing and synthesizing a nanocomposite with significant biocompatibility, biodegradability, and stability in biological microenvironments. Hence, the porous ultra-low-density materials, metal–organic frameworks (MOFs), have been considered and the MIL-125(Ti) has been chosen due to its distinctive characteristics such as great biocompatibility and good biodegradability immobilized on the surface of the reduced graphene oxide (rGO). Based on the results, the presence of transition metal complexes next to the drug not only can reinforce the stability of the drug on the structure by preparing π–π interaction between ligands and the drug but also can enhance the efficiency of the drug by preventing the spontaneous release. The effect of utilizing transition metal complex beside drug (Doxorubicin (DOX)) on the drug loading, drug release, and antibacterial activity of prepared nanocomposites on the P. aeruginosa and S. aureus as a model bacterium has been investigated and the results revealed that this theory leads to increasing about 200% in antibacterial activity. In addition, uptake, the release of the drug, and relative cell viabilities (in vitro and in vivo) of prepared nanomaterials and biomaterials have been discussed. Based on collected data, the median size of prepared nanocomposites was 156.2 nm, and their biological stability in PBS and DMEM + 10% FBS was screened and revealed that after 2.880 min, the nanocomposite's size reached 242.3 and 516 nm respectively. The MTT results demonstrated that immobilizing PdL beside DOX leads to an increase of more than 15% in the cell viability. It is noticeable that the AST:ALT result of prepared nanocomposite was under 1.5. [ABSTRACT FROM AUTHOR]

Background: Propionic acid as a very valuable chemical is in high demand, and it is industrially produced via the oxo-synthesis of ethylene or ethyl alcohol and via the oxidation of propionaldehyde with oxygen. It is urgent to discover a new preparation method for propionic acid via a green route. Recyclable amino-acid-based organic–inorganic heteropolyoxometalates were first used to high-efficiently catalyse the selective oxidation of 1-propanol to propionic acid with H2O2 as an oxidant. Result: A series of amino-acid-based heteropoly catalysts using different types of amino acids and heteropoly acids were synthesized, and the experimental results showed proline-based heteropolyphosphatotungstate (ProH)3[PW12O40] exhibited excellent catalytic activity for the selective catalytic oxidation of 1-propanol to propionic acid owing to its high capacity as an oxygen transfer agent and suitable acidity. Under optimized reaction conditions, the conversion of 1-propanol and the selectivity of propionic acid reached 88% and 75%, respectively. Over four cycles, the conversion remained at >80%, and the selectivity was >60%. (ProH)3[PW12O40] was also used to catalyse the oxidations of 1-butanol, 1-pentanol, 1-hexanol, and benzyl alcohol. All the reactions had high conversions, with the corresponding acids being the primary oxidation product. Conclusions: Proline-based heteropolyoxometalate (ProH)3[PW12O40] has been successfully used to catalyse the selective oxidation of primary alcohols to the corresponding carboxylic acids with H2O2 as the oxidant. The new developed catalytic oxidation system is mild, high-efficient, and reliable. This study provides a potential green route for the preparation propionic acid. [ABSTRACT FROM AUTHOR]

This study reports the synthesis, characterisation and antimicrobial activity of five novel silverN-heterocyclic carbene (Ag–NHC) complexes obtained byN-propylphthalimide and N-methyldioxane substituted benzimidazolium salts with silver oxide. The reactions were performed at room temperature for 24 h in the absence of light. The obtained complexes were identified and characterised by1H and13C NMR, FT-IR and elemental analysis techniques. The minimum inhibitory concentration (MIC) of the complexes was determined forE. coli, P. aeruginosa, E. faecalis, S. aureus, C. tropicalisandC. albicans in vitrothrough agar and broth dilution. The results indicated that these complexes exhibit antimicrobial activity. In particular, complex3presented the significant broad spectrum antimicrobial activity. [ABSTRACT FROM PUBLISHER]