Publications by authors named "L V Klimenko"

The known analytical solution describing a two-dimensional viscous flow with vortices under a driving force is generalized. It is shown that a periodic pattern of asymmetric vortices arises when the force amplitude exceeds a critical value. The transport of an ensemble of passive particles through the resulting structure has been studied.

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We study macroscopic behavior of populations of quadratic integrate-and-fire neurons subject to non-Gaussian noises; we argue that these noises must be α-stable whenever they are delta-correlated (white). For the case of additive-in-voltage noise, we derive the governing equation of the dynamics of the characteristic function of the membrane voltage distribution and construct a linear-in-noise perturbation theory. Specifically for the recurrent network with global synaptic coupling, we theoretically calculate the observables: population-mean membrane voltage and firing rate.

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Coupling of photoswitching with dynamic covalent chemistry enables control of the formation and cleavage of covalent bonds by light irradiation. -Aryloxyanthraquinones feature an exclusive ability to switch electrophilicity by interconversion between - and -quinone isomers, which was used for the first time for the implementation of a dynamic C-O bond. Photogenerated -isomers undergo a concerted -Michael addition of phenols to give hitherto unknown 4-hydroxy-10,10-diaryloxyanthracen-9-ones.

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Emerging applications of photochromic compounds demand new molecular designs that can be inspired by some long-known yet currently forgotten classes of photoswitches. In the present review, we remind the community about Peri-AryloxyQuinones (PAQs) and their unique photoswitching behavior originally discovered more than 50 years ago. At the heart of this phenomenon is the light-induced migration of an aromatic moiety (arylotropy) in peri-aryloxy-substituted quinones resulting in ana-quinones.

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A new efficient method was proposed for the synthesis of (18-crown-6)stilbene; the structure of the product was confirmed by X-ray diffraction analysis. In MeCN, this compound forms pseudodimeric complexes with -(2-ammonioethyl)-4-styrylpyridinium and -(3-ammoniopropyl)-4-styrylpyridinium diperchlorates via hydrogen bonding between the ammonium group and the crown ether oxygen atoms. The ammonioethyl derivative was synthesized for the first time.

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