Lifetimes and the dynamics of hydrogen bonds in liquid water

Based on Raman spectra of light, heavy, and half-heavy water in the region of O-H and O-D stretching vibrations and on the independent-oscillator model, it is shown that a peculiarity of the liquid state of water is the nonequivalence of O-H groups of water molecules in hydrogen bonding. The structure of liquid water and the mechanism of its molecular mobility are considered in this context.     

Untersuchung des Wachstumsmechanismus und der Vbertragungsreaktionen bei der Olefin-Polymerisation mit Ziegler-Natta-Katalysatoren. 1. Mitt. Bestimmung der Zahl der Wachstumszentren und der Geschwindigkeitskonstante

Ohne Zusammenfassung     

Specific features of the structure of a lanthanum nitrate complex with ethylenediamine

Anhydrous lanthanum nitrate and its complexes with one and two ethylenediamine molecules are calculated by the ab initio B3LYP/LANL2DZ quantum-chemical method. An ethylenediamine molecule is shown to coordinate preferentially through one amino group, and a hydrogen bond is formed between the coordinated amino and nitrato groups. An ethylenediamine complex of lanthanum nitrate is synthesized, and its composition and thermal stability are determined. The IR spectra of the ethylenediamine complex of lanthanum nitrate confirm the presence of the intramolecular hydrogen bond in this complex.     

Infrared spectra of menthoxyalkylchloro-(alkoxy)silanes and chlorosilylpropionic and chlorosilylisobutyric acid menthyl esters

Conclusions The IR spectra of methyl- and phenylchloromenthoxysilanes, menthoxypropylalkylehlorosilanes, menthoxypropyl- and menthoxyethylmethylethoxysilanes, and also chlorosilylpropionic and chlorosilylisobutyric acid menthyl esters were studied. Assignments of the frequencies for a number of vibrations were made.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 9, pp. 2151–2155, September, 1968.     

Regularities of Structure Formation in AA2024 Alloy During High-Intensity Plastic Deformation Under Conditions of Adhesion-Diffusion Friction Interaction

Russian Physics Journal - The results of model experimental studies of structural-phase changes in an AA2024 aluminum alloy after friction with a counter-body of a complex configuration are...     

Identification of peroxo groups in supramolecular layered structures as probed by Raman spectroscopy

Peroxide-containing supramolecular structures prepared by reacting lithium aluminum layered double hydroxides (Li-Al LDHs) with concentrated hydrogen peroxide solutions were characterized by Raman spectroscopy. These compounds were formulated as [LiAl₂(OH)₆](OH) · H₂O₂ · H₂O(I) and [LiAl₂(OH)₆](OOH) · H₂O₂ · H₂O(II). The frequencies 830 and 849 cm⁻¹ in the spectra of compounds I and II were assigned to O—C stretching vibrations in two nonequivalent peroxo groups. The band at 866 cm⁻¹ in compound II was assigned to O—O vibrations in the hydroperoxo group (OOH)⁻. Proceeding from calculated strength factors, we inferred that the O—O bond in the hydroperoxo group of compound II is stronger than in the H₂O₂ solvating group. Original Russian Text ? T.A. Tripol’skaya, I.V. Pokhabova, P.V. Prikhodchenko, G.P. Pilipenko, E.A. Legurova, N.A. Chumaevskii, 2009, published in Zhurnal Neorganicheskoi Khimii, 2009, Vol. 54, No. 3, pp. 513–515.     

Chemistry and polymerization of 1, 1, 3, 3-tetramethyl-1, 3-disila-2-oxaindane

Reaction of o-dichlorobenzene with dimethylmethoxychlorosilane and sodium leads to the isolation of dimethyl(o-chlorophenyl) methoxysilane, o-bis(bimethylmethoxysilyl)benzene, 1,1,3,3-tetramethyl-1,3-disila-2-oxaindane, and 1, 1-dimethyl-1-silarribenzocycloheptatriene. When I is polymerized with H₂SO₄, the phenyl group is observed to split off.