A study of 1,2,3,4-tetrahydro-4-azafluorene-3,9-diones

Intramolecular cyclization of the diamides and N,N-dimethylamides of -[indan-1,3-dion-2-yl]benzylmalonic acids (I) has given 1-aryl-2-carbamoyl-1,2,3,4-tetrahydro-4-azafluorene-3, 9-diones and 1-aryl-4-methyl-2-methylcarbamoyl-1,2,3,4-tetrahydro-4-azafluorene-3,9-diones (II). The structure of compounds II was shown by chemical methods: bromination, xanthylation, and hydrolysis in alkaline and acid media, and also by a study of IR and UV spectra.     

Autocatalytic oxidation of Fe(Phen)3 2+ by bromate in water-in-oil reverse micelles of AOT

Autocatalytic oxidation of ferroin by bromate in water-in-oil reverse micelles of AOT has been studied experimentally and theoretically. The simplest models for this process have been constructed. Analytical solutions for these models were found for some limiting cases. It has been shown that the autocatalytic reaction runs much more slowly in reverse micelles than in water. The dependencies of the maximum reaction rate, _max, the exponent of the increase in ferriin concentration, , and induction period, , on micelle concentration have been obtained at =[H₂O]/[AOT]=4.6. It was found that there is only one theoretical model which can explain the experimental data. The values of the elementary reaction rate constantsk _i were estimated on the basis of the theoretical dependencies of _max and on the constantsk _i . All elementary rate constants turned out to be two or three orders of magnitude smaller than the corresponding constants for the reaction proceeding in water. The decrease in the rate constants is explained by the increase in viscosity and pH in a micellar water core at low .Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1401–1407, August, 1993.This work was supported by the Russian Foundation for Fundamental Investigations through Research Grant 93-03-4090.     

Synthesis of derivatives of 1, 2, 3, 4-tetrahydro-4-azafluoren-3,9-diones

Cyclization of amides of -carbamido--(indan-1, 3-dione-2-yl) hydrocinnamic acid gives 1-aryl-2-carbamido-1, 2, 3, 4-tetrahydro-4-azafloren-3, 9-dione. Alkaline and acid hydrolysis of these compounds are investigated.     

Dash waves in a reaction-diffusion system

Patterns in reaction-diffusion systems generally consist of smooth traveling waves or of stationary, discontinuous Turing structures. Hybrid patterns that blend the properties of waves and Turing structures have not previously been observed. We report observation of dash waves, which consist of wave segments regularly separated by gaps, moving coherently in the Belousov-Zhabotinsky system dispersed in water-in-oil microemulsion. Dash waves emerge from the interaction between excitable and pseudo-Turing-unstable steady states. We are able to generate dash waves in simulations with simple models.     

Oscillatory clusters in the periodically illuminated, spatially extended Belousov-Zhabotinsky reaction

Cluster-cluster transitions in the periodically illuminated photosensitive Belousov-Zhabotinsky (BZ) reaction-diffusion system exhibit the same scenario as in the autonomous BZ system with negative global feedback: two-phase clusters <--> three-phase clusters <--> irregular clusters <--> localized clusters. Transitions induced by changing the dark ( TD) or light ( TL) phases of the periodic external square wave illumination are dependent not only on the frequency of illumination at constant TD/TL, but also on the ratio TD/TL at constant frequency (when TD+TL = const).     

Infrared spectra and enolization of simple 1, 3-diketones

The infrared spectra of simple nonsubstituted-diketones have been analyzed; this makes it possible to obtain information on their keto-enol equilibria. The ease of enolization of these-diketones changes considerably when a cyclic structure is formed, and depends on the dimensions of the ring. The nature of the enol bands in the infrared spectra is discussed.     

Polynuclear heterocyclic compounds

The cyclization of halogenophenyldiindanedionylmethanes to the corresponding halogenophenyldibenzoylenepyrans and dibenzoylenedihydropyridines is investigated. The latter are readily oxidized to dibenzoylenepyridines.For Part XX see [15].     

Discontinuously propagating waves in the bathoferroin-catalyzed Belousov-Zhabotinsky reaction incorporated into a microemulsion

Three new types of discontinuously propagating waves are reported in the bathoferroin-catalyzed Belousov-Zhabotinsky (BZ) reaction dispersed in water-in-oil Aerosol OT microemulsion. Jumping waves (JWs) are typically observed at or above room temperature and develop from the familiar trigger waves. Bubble waves (BWs) typically emerge from trigger or JWs at similar temperatures, while rotating waves (RWs) evolve from JW at higher temperatures (>40 degrees C). All these waves propagate discontinuously in a saltatory fashion. Other characteristic features include a discontinuous front for BW consisting of small concentric waves (bubbles) and lateral rotation of annular RWs. All three types of waves, as well as segmented but continuously propagating waves, can coexist. A simple model that is able to describe both jumping and segmented waves is described.     

Experimental Investigation of the Dynamical Modes of Four Pulse-Coupled Chemical Micro-Oscillators

We present an experimental system of four identical microreactors (MRs) in which the photosensitive oscillatory Belousov-Zhabotinsky (BZ) reaction occurs. The inhibitory coupling of these BZ MRs is organized via pulses of light coming to each MR from a computer projector. These pulses are induced by spike(s) in other MR(s) of the same network. Time delay between the spike in one BZ MR and the pulsed perturbation of the other BZ MR(s), the amplitude of light pulses, their duration, and the connectivity of the MRs are controlled by the LabVIEW software. Recording the dynamics of the BZ reaction in the MRs via a microscope equipped with a CCD camera, we observe all the main dynamical modes of our network of MRs, which are the IP (in-phase), AP (anti-phase), W (walk), and WR (walk reverse) for the unidirectional coupling, and the IP, two-cluster, three-cluster, and splay modes for the all-to-all coupling. Our software detects all the modes of the network automatically and makes it possible to switch between them on demand using a few special “switching” pulses. As the result of the present work, the experimental implementation of the adaptive behaviour of the pulse-coupled chemical micro-oscillator networks becomes available.