Experimental Study of Small-Scale Spatial Variation in Filtration Coefficient Using Tracer Method

The procedure for studying the nonuniformity of filtration flows in capillary-porous media was developed. Time dependences of local filtration coefficients averaged over the area and their spatial variation during the flow of water and aqueous electrolyte solutions were studied on soil samples of undisturbed structure using tracer method. It was found that the transformation of a pore space structure accompanied with reverse variations in pore sizes occurs because of the action of disjoining pressure in thin films depending on the ion nature. Relaxation times corresponding to the times necessary to attain equilibrium within interlayer gaps of clay minerals were determined. The conclusion was made that if the system volume is constant, the variations in the pore space structure take place because of decrease in the relative fraction of macropores and their sizes.     

Exchange and magnetic dipole-dipole interactions in bi- and triradical complexes of Al(III), Ga(III), In(III), and Sn(IV) witho-semiquinones. PM3 calculation

Semiempirical (PM3 with CI) calculations of exchange interactions for the triradical complexes of Al(III), Ga(III), and In(III) and the biradical complex of Sn (IV) with o-semiquinones are carried out. The results are in agreement with both qualitative theoretical assumptions and experimental data. The calculations indicate that the superexchange via the unoccupied porbitals of the central metal ion predominantly determines the multiplicity of the ground states of the complexes. Zero-field splitting constants D are calculated; they also agree well with experimental data. Deceased. Translated fromZhumal Struktumoi Khimii, Vol. 38, No. 6, pp. 1053–1060, November–December, 1997.     

Kinetics and products of the reaction of diazo compounds with SO2

Data were obtained on the composition of products and kinetics of the reaction of SO₂ with Ph(R)CN₂ (R=Ph, Me) in solutions of isooctane, 1,4-di-oxane, and ethanol at 295 K. A mechanism was proposed for the process in accordance with which the sulfene being formed participates in concurrent reactions with the starting reagents. The relative rate constants for the process stages were determined.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 11, pp. 2496–2500, November, 1990.