The mechanochemical preparation of highly functionalized 3,5-disubstituted hydantoins was investigated in the presence of various poly(ethylene) glycols (PEGs), as safe grinding assisting agents (liquid-assisted grinding, LAG). A comparative study under dry-grinding conditions was also performed. The results showed that the cyclization reaction was influenced by the amount of the PEG grinding agents. In general, cleaner reaction profiles were observed in the presence of PEGs, compared to dry-grinding procedures.

Allyl alcohol (AA) was obtained by the deoxydehydration (DODH) of glycerol performed in the presence of a number of Re compounds (oxides, phosphine and halide derivatives) in alcoholic solvent or in neat conditions. Independently of starting Re species, the resulting catalytic process featured a delay time, necessary to start the formation of both AA and an Re-alkoxide precipitate. However, no delay time was detected by operating DODH using a preformed precipitate obtained by either Re source. As a consequence, and based on IR spectral analysis, it was hypothesized that the Re precipitate is the actual catalyst of DODH. The mechanism of DODH catalysis operated by methyltrioxorhenium (MTO) was studied by experimental and theoretical approaches. The results suggest that MTO releases methane with the formation of an Re^VII alkoxide that subsequently aggregates by yielding the precipitate. The Re^VII centre precipitate surface then undergoes reduction by forming Re^V catalytic spots. The calculated kinetics also indicate that the detected latency can be ascribed to the presence of two high barriers, i.e. methane release and Re^VII → Re^V reduction, whereas the downstream processes, i.e. glycation and AA release, are not rate determining.

A new easy protocol to functionalize the middle layer of commercial surgical face masks (FMs) with Zn and Cu oxides is proposed in order to obtain antibacterial personal protective equipment. Zinc and copper oxides were synthesized embedded in a polydopamine (PDA) shell as potential antibacterial agents; they were analyzed by XRD and TEM, revealing, in all the cases, the formation of metal oxide nanoparticles (NPs). PDA is a natural polymer appreciated for its simple and rapid synthesis, biocompatibility, and high functionalization; it is used in this work as an organic matrix that, in addition to stabilizing NPs, also acts as a diluent in the functionalization step, decreasing the metal loading on the polypropylene (PP) surface. The functionalized middle layers of the FMs were characterized by SEM, XRD, FTIR, and TXRF and tested in their bacterial-growth-inhibiting effect against Klebsiella pneumoniae and Staphylococcus aureus. Among all functionalizing agents, Cu₂O-doped-ZnO NPs enclosed in PDA shell, prepared by an ultrasound-assisted method, showed the best antibacterial effect, even at low metal loading, without changing the hydrophobicity of the FM. This approach offers a sustainable solution by prolonging FM lifespan and reducing material waste.

Renewal in the world production of plastics with growing amounts of building blocks from biomass is a pressing demand among society. Adipic acid is one of the monomers of nylon 6,6, and, traditionally, is obtained from fossil sources, but it is possible to reduce the muconic acids, deriving it from biomass, to obtain adipic acid. However, these catalyzed reactions use commonly hazardous conditions or reagents; in this study, a pathway to obtain a bio-adipic acid, following the Green Chemistry, is reported. Metal nanoparticles (M NPs; M = Pd, Pt, Ru, Rh) were synthesized in water at 80 °C using sodium lignosulphonate as a reducing and stabilizing agent. They were characterized by TEM and XRD techniques: Pd NPs were larger (21 nm) and spherical in shape; Pt NPs were irregular; Ru and Rh NPs were smallest (1.9 and 5.3 nm, respectively). M NPs were tested as catalyst in the hydrogenation reactions of dicarboxylic acids (fumaric, malonic, trans,trans- and cis,cis-muconic acids) in water at room pressure and temperature. The NPs transformed selectively fumaric and malonic acids to succinic acid, although with different yields. Ru and Pt NPs were moderately active while with Pd NPs, 80% of succinic acid was obtained and with Rh NPs, 100% was observed. Carrying out the hydrogenations on muconic acids at pH 5, the formation of adipic acid was observed with all NPs but selectivities in the presence of Ru, Pt and Pd NPs were not excellent. The selectivity with Rh NPs was remarkable (86% from cis,cis- and about 100% from trans,trans-muconic acid) considering the mild conditions; furthermore, it is attractive that the adipic acid was obtained also from the cis,cis isomer which can be produced from biomass.