Materials possessing long-term antibacterial behavior and high cytotoxicity are of extreme interest in several applications, from biomedical devices to food packaging. Furthermore, for the safeguard of the human health and the environment, it is also stringent keeping in mind the need to gather good functional performances with the development of ecofriendly materials and processes. In this study, we propose a green fabrication method for the synthesis of silver nanoparticles supported on oxidized nanocellulose (ONCs), acting as both template and reducing agent. The complete structural and morphological characterization shows that well-dispersed and crystalline Ag nanoparticles of about 10–20 nm were obtained in the cellulose matrix. The antibacterial properties of Ag-nanocomposites (Ag–ONCs) were evaluated through specific Agar diffusion tests against E. coli bacteria, and the results clearly demonstrate that Ag–ONCs possess high long-lasting antibacterial behavior, retained up to 85% growth bacteria inhibition, even after 30 days of incubation. Finally, cell viability assays reveal that Ag-ONCs show a significant cytotoxicity in mouse embryonic fibroblasts.

This work focuses on the possible application of gold nanoparticles on flexible cotton fabric as acetone- and ethanol-sensitive substrates by means of impedance measurements. Specifically, citrate- and polyvinylpyrrolidone (PVP)-functionalized gold nanoparticles (Au NPs) were synthesized using green and well-established procedures and deposited on cotton fabric. A complete structural and morphological characterization was conducted using UV–VIS and Fourier transform infrared (FT–IR) spectroscopy, atomic force microscopy (AFM), and scanning electron microscopy (SEM). A detailed dielectric characterization of the blank substrate revealed interfacial polarization effects related to both Au NPs and their specific surface functionalization. For instance, by entirely coating the cotton fabric (i.e., by creating a more insulating matrix), PVP was found to increase the sample resistance, i.e., to decrease the electrical interconnection of Au NPs with respect to citrate functionalized sample. However, it was observed that citrate functionalization provided a uniform distribution of Au NPs, which reduced their spacing and, therefore, facilitated electron transport. Regarding the detection of volatile organic compounds (VOCs), electrochemical impedance spectroscopy (EIS) measurements showed that hydrogen bonding and the resulting proton migration impedance are instrumental in distinguishing ethanol and acetone. Such findings can pave the way for the development of VOC sensors integrated into personal protective equipment and wearable telemedicine devices. This approach may be crucial for early disease diagnosis based on nanomaterials to attain low-cost/low-end and easy-to-use detectors of breath volatiles as disease markers.

Copper is widely used in both its metallic form and as oxide across numerous scientific and industrial domains. The primary copper oxides, cuprite (Cu₂O) and tenorite (CuO), naturally form on the copper surface and play a crucial role in advanced technologies, such as solar cells, lithium batteries, and sensors. Tenorite is appreciated for its optical properties, stability, low toxicity, and reactivity. While copper oxide thin films are traditionally synthesized through thermal treatments and oxidation in alkaline environments, these conventional high-temperature methods not only require significant energy consumption but can also compromise the metal–film interface. This study aims to develop a sustainable alternative approach for forming a homogeneous CuO layer on a copper substrate through environmentally friendly treatments based on low temperature, cost-effective, and time-saving procedures. Three different eco-conscious treatments were investigated: (i) immersion in NaOH basic solution, (ii) exposure to NaOH basic solution vapours, and (iii) a combined treatment involving both immersion and vapour exposure. This green synthesis approach significantly reduces energy consumption compared to traditional thermal methods while maintaining product quality. The surface oxide layer was investigated through an optical microscope (OM), scanning electron microscopy (SEM), spectrocolorimetric analysis, peel-off test, µ-Raman and X-ray photoelectron spectroscopy (XPS) analysis to investigate the surface oxidation state.

The synthesis of a new chiral agent, (R,R) (-)N, N'-trans-1, 2-dihexylcyclohexanediamine, for the chromatographic resolution of racemates is reported. Highly selective separations of D- and L-isomers of free and Dns-amino acids were accomplished on a reversed-phase column using in the mobile phase a Cu(II) complex of the above chiral selector. The procedure was extended to resolve diastereomeric derivatives, which were obtained by reaction of an optically active amine with o-phthaldeyde in the presence of N-acetyl-L-cysteine.