The results of sensing of the gas and aerosol composition of the atmosphere with the Optik Tu‐134 aircraft laboratory in the period from 31 July to 1 August 2012 are presented. The measurements were conducted along the flight route Novosibirsk‐Tomsk‐Mirny‐Yakutsk‐Bratsk‐Novosibirsk. A significant part of the Siberian territory during this period was covered by numerous forest fires. The synoptic situation during the measurements was characterized by the presence of low‐gradient field. This fact determined the low rate of transport and diffusion of pollutants and their accumulation in the region under study. The maximal concentrations of CO2, CH4, and CO over fire zones achieved 432 ppm, 2367 ppb, and 4036 ppb, respectively. The aerosol particle number density in emission plumes achieved 4400 cm−3. Outside emission plumes, the concentration ranged within 400–1000 cm−3 depending on the region. The mass concentration of aerosol in plumes increased approximately 7 times (6.9). The enrichment of the concentration of some elements and ions in the plume with respect to the background varied from 1.3 to 9.1 times. The generation of ozone from biomass burning products was observed at plume boundaries. Two versions of this process are possible: ozone generation under and above the plume.

Information on the ozone concentration in the surface air and troposphere in the first half of 2020 is presented. The data were acquired at 13 stations in different Russian regions; vertical distributions were obtained with the use of an aircraft laboratory. The excess over the Russian Federation hygienic standards is assessed; the daily average ozone concentration is found to be regularly higher the maximum permissible concentrations at most stations. At some stations, there are features the seasonal variations in the ozone concentration in the period under study different from previous years.

The highly effective self-assembly process between 2,4,6-tris(isopropyl)phenylphosphine or mesitylphosphine, formaldehyde and 1,4-bis(alpha-(4'-aminophenyl)isopropyl)benzene results in the formation of a novel type of heterocyclophane which is able to encapsulate organic molecules as well as being a potential ligand for transition metals inside the intramolecular cavity. Compounds of this type can be regarded as potential precursors for a new kind of molecular reactors.

Protonation (alkylation) sites of several thiopyrimidine derivatives were directly determined by 1H-15N (1H-13C) heteronuclear single quantum coherence/heteronuclear multiple bond correlation methods, and it was found that in all compounds, protonation (methylation) occurred at the N1 nitrogen. GIAO DFT chemical shifts were in full agreement with the determined tautomeric structures. According to ab initio calculations, the stability of the different protonated forms and methylated derivatives was favored due to thermodynamic control and not kinetic control.