Reaction of aroylenebenzimidazoles with nucleophilic reagents

The reaction of aromatic mono- and bis(o-phenylenediamines), -(aminophenols), and -(o-aminothiophenols) with mono- and diaroylenebenzimidazoles in polyphosphoric acid was studied. The interrelationship between the structures and properties of the resulting compounds, which contain benzimidazole and other rings in the ortho position relative to one another, was investigated.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 247–252, February, 1972.     

Asymmetric fission of the pre-actinide nuclei

Study of α particles, protons and neutrons emission in reactions induced by¹⁶O on Sn targets. The threshold for direct a emission is found to be v/c?0.04 (v velocity of the projectile at the top of the Coulomb barrier) whereas direct protons and neutrons, if any, would be emitted for beam energies higher than 7.8MeV/n. (v/c>0.092). Atv/c 0.092, 90% of the direct a cross section is shown to be incomplete fusion. On¹¹⁶Sn target, besides the main exit channels α4n and αp4n, we observed 2α4n and α2p4n channels where the direct α is followed by evaporation particles. This implies a lower initial angular momentum than for the main channels.     

Association Phenomena of Poly(arylene ether sulfone)s in Dimethylformamide

Three poly(arylene ether sulfone)s (two polymers and one copolymer) containing diphenylfluorene, phenolphthalein and 2,4-bis[(4-chlorophenyl)sulfonyl]-1-(phenyltio) benzene)] units were synthesized by the classical Williamson polyetherification reaction. The association phenomenon in N,N-dimethylformamide (DMF) was investigated by different methods: gel permeation chromatography (GPC), viscosity, atomic force microscopy (AFM), fluorescence spectroscopy and dynamic light scattering (DLS). Both AFM and DLS measurements evidenced the formation of aggregates with spherical or ellipsoidal shape at a concentration around 0.05 wt.%. This behavior could be explained by dipole-dipole interactions between macromolecular chains, probably with the participation of solvent molecules, and by H-bonds involving hydroxyl end groups.     

Sulfanyl chloride induced heterocyclization of N-(pyrazolyl)styrylacetamides

Heterocyclization of N-(pyrazol-3-yl)styrylacetamides with arenesulfenyl chlorides yields the corresponding tetrahydrofuran-2-iminium perchlorates isolable after chromatography as trans-5-aryl-4-(arylthio)tetrahydrofuran-2-ones and 5-aryl-4-(arylthio)-1-(pyrazol-3-yl)pyrrolidin-2-ones, with the latter predominating. N-(Pyrazol-4-yl)styrylacetamides react under analogous conditions to give 5-aryl-4-(arylthio)-1-(pyrazol-4-yl)pyrrolidin-2-ones, 4-aryl-3-(arylthio)-4-chloro-N-(1-methylpyrazol-4-yl)butanamides, and tetrahydrofuran-2-iminium perchlorates which, when chromatographed, produce 5-aryl-4-(arylthio)dihydrofuran-2(3H)-ones and 4-aryl-3-(arylthio)-4-methoxy-N-(1-methyl-1H-pyrazol-4-yl)butanamides.     

Observation of the magnetic domain structure in Cu<Subscript>0.47</Subscript>Ni<Subscript>0.53</Subscript> thin films at low temperatures

We report on the first experimental visualization of domain structure in films of weakly ferromagnetic Cu_0.47Ni_0.53 alloy with different thickness at liquid helium temperatures. Improved high-resolution Bitter decoration technique was used to map the magnetic contrast on the surface of the films well below the Curie temperature T_Curie (∼60 K). In contrast to magnetic force microscopy, this technique allowed visualization of the domain structure without its disturbance while the larger areas of the sample were probed. Maze-like domain patterns, typical for perpendicular magnetic anisotropy, were observed. The average domain width was found to be about 100 nm. The article is published in the original.