Recently, pharmaceutical research has been focused on the design of new antibacterial drugs with higher selectivity towards several strains. Major issues concern the possibility to obtain com-pounds with fewer side effects, at the same time effectively overcoming the problem of antimi-crobial resistance. Several solutions include the synthesis of new pharmacophores starting from piperazine or morpholine core units. Mass spectrometry-based techniques offer important sup-port for the structural characterization of newly synthesized compounds to design safer and more effective drugs for various medical conditions. Here, two new piperazine derivatives and four new morpholine derivatives were synthesized and structurally characterized through a combined approach of FT-ICR and LTQ mass spectrometry. The support of both high-resolution and low-resolution mass spectrometric data namely accurate mass measurements, isotopic distribu-tion and MSn spectra, was crucial to confirm the success of the synthesis. These compounds were further evaluated for inhibitory activity against a total of twenty-nine Gram-positive and Gram-negative bacteria to determine the action spectrum and the antimicrobial effectiveness. Results demonstrated compounds’ antimicrobial activity against many tested bacterial species, providing an inhibitory effect linked to different chemical structure and suggesting that the new-synthesized derivatives could be considered as promising antimicrobial agents.

A new tetracyclic morpholine-fused [5,1-c]-triazole, (4aS,5S,6aR,10aR,10bR)-5-methoxy-9,9-dimethyl-4a,5,6a,7,10a,10b-hexahydro-12H-[1,3]dioxino[4',5':5,6]pyrano[4,3-b][1,2,3]triazolo[1,5-d][1,4]oxazine, was synthesized via a five-step sequence starting from methyl α-D-glucopyranoside by using as a key step an intramolecular copper(I) cat-alyzed alkyne-azide cycloaddition (CuAAC). The synthesized compound was fully characterized by 1H and 13C NMR, FT-IR, and HRMS.

Electrolysis of water is one of low-cost green hydrogen production technologies. The challenge is designing and developing low-cost and high-activity catalysts. Herein, we present a strategy to fabricate flexible electrocatalysts based on nickel-iron (NiFe) alloy coatings. NiFe coatings were plated on the flexible copper-coated polyimide surface (Cu/PI) using the low-cost and straightforward electroless metal plating method and morpholine borane as a reducing agent. It was found that Ni90Fe10, Ni80Fe20, Ni60Fe40, and Ni30Fe70 coatings were deposited on the Cu/PI surface, then the concentration of Fe2+ in the plating solution was 0.5 mM, 1 mM, 5 mM, and 10 mM, respectively. Morphology, structure, and composition of NixFey/Cu/PI catalysts have been examined using scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), and inductively coupled plasma optical emission spectroscopy (ICP-OES), whereas their activity has been investigated for hydrogen evolution (HER) and oxygen evolution (OER) reactions in 1 M KOH using linear sweep voltammetry (LSVs). It was found that the Ni80Fe20/Cu/PI catalyst exhibited the lowest overpotential value of –202.7 mV for the HER to obtain a current density of 10 mA cm–2 compared to Ni90Fe10/Cu/PI (–211.9 mV), Ni60Fe40/Cu/PI (–276.3 mV), Ni30Fe70/Cu/PI (–278.4 mV), and Ni (−303.4 mV). On the other hand, the lowest OER overpotential (344.7 mV) was observed for the Ni60Fe40/Cu/PI catalyst to obtain a current density of 10 mA cm–2 as compared with the Ni30Fe70 (369.9 mV), Ni80Fe20 (450.2 mV), Ni90Fe10 (454.2 mV) coatings, and Ni (532.1 mV). The developed Ni60Fe40/Cu/PI catalyst exhibit a cell potential of 1.85 V at 10 mA cm−2. The obtained catalysts seem to be suitable flexible catalysts for HER and OER in alkaline media.