Effective microwave-assisted approach to 1,2,3-triazolobenzodiazepinones via tandem Ugi reaction/catalyst-free intramolecular azide–alkyne cycloaddition

A novel catalyst-free synthetic approach to 1,2,3-triazolobenzodiazepinones has been developed and optimized. The Ugi reaction of 2-azidobenzaldehyde, various amines, isocyanides, and acids followed by microwave-assisted intramolecular azide–alkyne cycloaddition (IAAC) gave a series of target heterocyclic compounds in moderate to excellent yields. Surprisingly, the normally required ruthenium-based catalysts were found to not affect the IAAC, only making isolation of the target compounds harder while the microwave-assisted catalyst-free conditions were effective for both terminal and non-terminal alkyne

2D Molybdenum Carbide MXenes for Enhanced Selective Detection of Humidity in Air

2D transition metal carbides and nitrides (MXenes) open up novel opportunities in gas sensing with high sensitivity at room temperature. Herein, 2D Mo2CTx flakes with high aspect ratio are successfully synthesized. The chemiresistive effect in a sub-mu m MXene multilayer for different organic vapors and humidity at 10(1)-10(4) ppm in dry air is studied. Reasonably, the low-noise resistance signal allows the detection of H2O down to 10 ppm. Moreover, humidity suppresses the response of Mo2CTx to organic analytes due to the blocking of adsorption active sites. By measuring the impedance of MXene layers as a function of ac frequency in the 10(-2)-10(6) Hz range, it is shown that operation principle of the sensor is dominated by resistance change rather than capacitance variations. The sensor transfer function allows to conclude that the Mo2CTx chemiresistance is mainly originating from electron transport through interflake potential barriers with heights up to 0.2 eV. Density functional theory calculations, elucidating the Mo2C surface interaction with organic analytes and H2O, explain the experimental data as an energy shift of the density of states under the analyte's adsorption which induces increasing electrical resistance

Synthesis of 5-Cinnamoyl-3,4-dihydropyrimidine-2(1H)-ones

<div><p></p><p>Two different approaches to the synthesis of 1-unsubstituted 5-cinnamoyl-3,4-dihydropyrimidine-2(1H)-ones have been developed. The first includes N(1)-protection of the starting 5-acetyl-3,4-dihydropyrimidine-2(1H)-one, further Claisen–Schmidt reaction, and cleavage of the protecting group. The second approach consists of one-pot condensation of urea, aldehyde, and cinnamoylacetone as dicarbonyl component. The 5-cinnamoylderivative synthesis starting from 5-acetyl-1,3-dialkyl-3,4-dihydropyrimidine-2(1H)-ones is also shown.</p> </div

Quasi-2D Co3O4 nanoflakes as an efficient gas sensor

Here, we study quasi-two-dimensional crystals of Co3O4 grown by electrochemical synthesis on Pt electrodes with a nanoflake morphology to serve as a gas sensor. When synthesizing in aqueous electrolytes under applied electrical bias, the material follows a self-hierarchical architecture to primarily appear as the hexagonal nanoflakes α-Co(OH)2. After heating up to 300 °C in air, the as-synthesized material transforms to Co3O4, preserving the original hierarchical morphology. The Co3O4 nanoflakes have been found to have remarkable chemiresistive response when exposed to various kinds of alcohol vapors, at low ppm concentrations in a mixture with air, over a wide range of temperatures up to 300 °C with a detection limit down to the ppb range with direct dependence on the molecule weight of the alcohol. We explain the observed features of the gas response of the Co3O4 nanoflakes by a shift in the electron density under the chemisorption of VOCs, verified by DFT calculations.Peer reviewe