Nonreciprocity of losses and shift of the zero point in a laser gyroscope

Results of calculations of intensities, losses, and frequencies of counterpropagating waves in a ring resonator containing a weakly nonlinear active medium and an aperture are given. It is shown that inequalities of frequencies and intensities of generation of counterpropagating waves occur in such a resonator. The behavior of these inequalities is determined by the nonreciprocity of frequency-dependent losses of the counterpropagating waves.     

Synthesis of N-Vinyloxyalkyl Imines

Russian Journal of Organic Chemistry -     

DICSI station at KCSR and NT: Determination of optimal requirements to the formation of an SR beam using cylindrical x-ray optical zoom lenses

To modernize the DICSI station, new hardware and software have been created according to the conditions of the operating storage ring “Sibir’-2” beam channel. The recording system has been successfully tested on the operating channel of the storage ring VEPP-3 (Budker Institute of Nuclear Physics Siberian Branch, Russian Academy of Sciences, Novosibirsk) using the time-resolved “diffraction cinema” technique in studying real biological objects in the static and dynamic modes of data accumulation. At the DICSI station, structural changes in medical and biological objects are permanently investigated. The specific structure dimensions of these objects are in the nanometric range.     

N,N'-Bis(vinyloxyalkyl) Dicarboxamides

N,N'-Bis(vinyloxyalkyl)oxamides and N,N'-bis(vinyloxyalkyl)phthalamides were synthesized in 60-95% yield by reactions of vinyloxyalkylamines with diethyl oxalate and phthalimide, respectively.     

Reaction of vinyloxyalkylamines with mercaptoacetic acid

N-[2(3)-Hydroxyalkylj-4-thiazolidinones have been synthesized by the reaction of 2(3)-vinyloxyalkylamines with mercaptoacetic acid in 24–69 % yield. The structure of the compounds obtained was supported by (R and¹H NMR spectroscopic data.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 3, pp. 677–679, March, 1996.     

(2-Vinyloxyethyl)hydrazines

Reaction of hydrazine hydrate with 2-chloroethyl vinyl ether afforded (2-vinyloxyethyl)hydrazine and 1,1-bis(2-vinyloxyethyl)hydrazine in 20-38% yield.     

Synthesis of 5-hydroxy-N-(2-vinyloxyalkyl)indoles from dicarbonyl compounds and vinyloxyalkylamines

N-(Vinyloxyalkyl)enaminoketones were obtained by the condensation of vinyloxyalkylamines with acetylacetone or ethyl acetoacetate. Their subsequent reactions with 1,4-benzoquinone produce the corresponding 5-hydroxy-2-methyl-N-(2-vinyloxyalkyl)indoles in 17–43% yields. The structures of the compounds obtained were confirmed by IR and¹H NMR spectroscopy.