Experimental Simulation of the Radionuclide Behaviour in the Process of Creating Additional Safety Barriers in Solid Radioactive Waste Repositories Containing Irradiated Graphite

Results of the experimental modeling of radionuclide behavior when creating additional safety barriers in solid radioactive waste repositories are presented. The experiments were run on the repository mockup containing solid radioactive waste fragments including irradiated graphite. The repository mockup layout is given; the processes with radionuclides that occur during the barrier creation with a clayey solution and during the following barrier operation are investigated. The results obtained confirm high anti-migration and anti-filtration properties of clay used for the barrier creation even under the long-term excessive water saturation of rocks confining the repository

Synthesis and Antimicrobial Activity of Sulfenimines Based on Pinane Hydroxythiols

The widespread presence of multidrug-resistant pathogenic microorganisms challenges the development of novel chemotype antimicrobials, insensitive to microbial tools of resistance. To date, various monoterpenoids have been shown as potential antimicrobials. Among many classes of molecules with antimicrobial activity, terpenes and terpenoids are an attractive basis for the design of antimicrobials because of their low toxicity and availability for various modifications. In this work, we report on the synthesis of sulfenimines from chiral trifluoromethylated and non-fluorinated pinane-type thiols. Final compounds were obtained with yields of up to 81%. Among the 13 sulfenimines obtained, 3 compounds were able to repress the growth of both bacteria (S. aureus, both MSSA and MRSA; P. aeruginosa) and fungi (C. albicans) with an MIC of 8–32 µg/mL. Although compounds exhibited relatively high cytotoxicity (the therapeutic index of 3), their chemotype can be used as a starter point for the development of disinfectants and antiseptics for targeting multidrug-resistant pathogens

Synthesis and Biological Activity of Unsymmetrical Monoterpenylhetaryl Disulfides

New unsymmetrical monoterpenylhetaryl disulfides based on heterocyclic disulfides and monoterpene thiols were synthesized for the first time in 48–88% yields. Hydrolysis of disulfides with fragments of methyl esters of 2-mercaptonicotinic acid was carried out in 73–95% yields. The obtained compounds were evaluated for antioxidant, antibacterial, antifungal activity, cytotoxicity and mutagenicity