Heterocyclization of 1,1-dicyano-2-(trifluoromethyl)ethylenes with 1,3,3-trimethyl-3,4-dihydroisoquinoline and its derivatives

1,3,3-Trimethyl-3,4-dihydroisoquinolines react with 1,1-dicyano-2,2-bis(trifluoromethyl)ethylene to give 4-amino-6,6-dimethyl-2,2-bis(trifluoromethyl)-3-cyano-6,7-dihydro-2H-benzo[a]quinolizines. The reaction of 3,3-dimethyl-1-cyanomethylidene-1,2,3,4-tetrahydroisoquinoline and the methyl ester of 3,3-dicyano-2-(trifluoromethyl)acrylic acid leads to 5,5-dimethyl-3-oxo-2-(trifluoromethyl)-2-(dicyanomethyl)-2,3,5,6-tetrahydropyrrolo[2,1-a]isoquinoline.A. N. Nesmeyanov Institute of Heteroorganic Compounds, Russian Academy of Sciences, 117813 Moscow. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 8, pp. 1888–1892, August, 1992.     

Reaction of chlorine fluosulfate with fluorinated alcohols and some properties of polyfluoroalkyl hypochlorites

Conclusions Stable ,-dihydropolyfluoroalkyl hypochlorites were obtained by reacting ClOSO₂F with fluorinated alcohols, and some of their chemical properties were studied.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 10, pp. 2369–2374, October, 1980.     

Acoustic and NMR investigations of melting and crystallization of indium–gallium alloys in pores of synthetic opal matrices

The paper presents the results of studying the crystallization and melting processes of Ga–In eutectic alloys, which are embedded in opal matrices, using acoustic and NMR methods. The indium concentrations in the alloys were 4, 6, 9, and 15 at %. Measurements were performed upon cooling from room temperature to complete crystallization of the alloys and subsequent heating. It is revealed how the size effects and alloy composition influence the formation of phases with α- and β-Ga structures and on changes in the melting-temperature ranges. A difference was observed between the results obtained using acoustic and NMR methods, which was attributed to different temperature measurement conditions.     

Local atomic structure of niobates and titanates from X-ray absorption spectroscopic data

The local atomic structure of PbTiO₃, BaTiO₃, and KNbO₃ perovskite-type crystals and K _x Na_{1 ? x} NbO₃ solid solutions in different phases is investigated using the angular dependence of the pre-edge structure of the Ti and Nb K X-ray absorption spectra and the EXAFS data. In noncubic phases, a considerable deviation of the local structure from the structure determined from diffraction data is observed only for the tetragonal phase of the BaTiO₃ crystal. It is revealed that, in the cubic phase of niobates, the niobium atoms are characterized by significant displacements from the centrosymmetric positions along the threefold axes, so that they are close in the magnitude and the direction to the displacements in the low-temperatures rhombohedral phases.     

Numerical modeling of the reflection coefficients for the plane sound wave reflection from a layered elastic bottom

The matrix method and its numerical realization are considered in calculating the complex reflection coefficients and refraction indices of plane sound waves for geoacoustic models of the ocean bottom in the form of homogeneous elastic (liquid) absorbing layers overlying an elastic halfspace. In calculating the reflection coefficients at high frequencies or in the presence of a large numbers of sedimentary layers, a passage from the Thomson-Haskell matrix approach to the Dunkin-Thrower computational scheme is performed. The results of test calculations are presented. With the aim of developing resonance methods for the reconstruction of the parameters of layered elastic media, the behavior of the frequency-angular dependences of the reflection coefficient are studied for various geoacoustic bottom models. The structure of the angular and frequency resonances of the reflection coefficients is revealed. The dependence of the structure (the position, width, and amplitude) of two types of resonances on the parameters of the layered bottom is considered.     

Pseudotetrahedral polyhaloadamantanes as chirality probes: synthesis,separation, and absolute configuration

Pseudotetrahedral, conformationally as well as configurationally stable 1-bromo-3-chloro-5-fluoro- (4) and 1-bromo-3-chloro-5-fluoro-7-iodoadamantane (5) (and some related compounds) were prepared by our recently devised phase-transfer catalytic halogenation protocol; the optical antipodes of 4 were separated by HPLC on chiral phase in ee > 99%, and the absolute configurations were assigned by matching observed and computed circular dichroism spectra. Structure 5 is the first chiral aliphatic hydrocarbon containing all stable (nonradioactive) halogens; its structure was proven by NMR spectroscopy and by X-ray crystal data. We emphasize that the combination of experiment and theory is very powerful in assigning absolute configurations even for molecules without typical chromophors, with small values for the optical rotation, and without an atom at the stereogenic center.     

Reactions of polyfluorocarbonyl compounds and their trifluoroacetylimines with fused heterocycles

C-Hydroxy- andC-aminoalkylation of iminodibenzyl, iminostilbene, phenoxazine, and phenothiazine with hexafluoroacetone, methyl trifluoropyruvate, and their trifluoroacetylimines were investigated. The substitution occurred at one or severalpara- andortho-positions to the N atom of the heterocycles. In the case of methyl trifluoropyruvate and its derivative the substitution in theortho-position was accompanied by the formation of lactams.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 1239–1242, May, 1996.