Polysaccharides of algae 68. Sulfated polysaccharides from the Kamchatka brown alga Laminaria bongardiana

Several fucoidan fractions were isolated from the biomass of the Kamchatka brown alga Laminaria bongardiana by hot water extraction followed by anion-exchange chromatography. Fucoidans were found to be composed of l-fucose, d-galactose, and sulfate as the major components, whereas d-xylose, d-mannose, d-glucuronic acid, and acetate were detected as the minor constituents. Highly sulfated fucoidan fractions F-2 and F-3 were solvolytically desulfated by heating in dimethyl sulfoxide in the presence of pyridine. The structures of native and desulfated polysaccharides were investigated by the methylation analysis and NMR spectroscopy. It was shown that F-2 contains fucan sulfate, the backbone of which is made of 1→3-linked α-l-fucopyranose residues with single α-l-Fucp branches at positions 2 and sulfate groups predominantly at positions 4. Sulfated fucoglucuronomannan, fucoglucuronan, and fucogalactan were detected in F-2 as concomitant polysaccharides. Fucan sulfate and sulfated fucogalactan were the major components of the fraction F-3. The anticoagulant properties of fucoidan fractions were assessed. It was demonstrated that the activity of the fraction F-3 is comparable with that of low-molecular-weight heparin (enoxaparin), whereas the activity of total fucoidan F and the fraction F-2 is ~2/3 and ~1/2, respectively, of the activity of F-3, which is in accordance with the lower sulfate content in these samples. Desulfated preparations F-2deS and F-3deS were completely devoid of anticoagulant activity.

     

Extracting model parameters from experimental data using the minimum information principle

A method is described for extracting model parameters of a physical process from statistical experimental data based on the minimum information principle. Potentialities of the method are studied by examples of regular and chaotic processes simulated by the transport and diffusion equation and by the logistic mapping.     

Anomalous Decrease in the Threshold of Stimulated Raman Scattering near the Surface of Liquid Nitrogen

JETP Letters - An anomalously strong (up to 13 times) reduction of the threshold of the stimulated Raman scattering of 15-ps laser pulses in liquid nitrogen has been found when moving the caustic...     

Density-functional theory calculation on the nitrogen oxide reduction reaction with carbon monoxide on a titanium dioxide nanocluster

The density functional theory was used for simulation of the NO reduction reaction with carbon monoxide on a reduced Ti₈O₁₅ nanocluster. The reaction proceeds on oxygen vacancies formed via the removal of terminal or bridging O atoms. In the case of adsorption of two NO molecules of such sites, a stable adsorption complex with the bidentate ligand ‥ONNO is produced. When a CO molecule approaches one of the O atoms of this cycle, the following exothermic reaction yielding N₂ and CO₂ adsorbed on the Ti₈O₁₆ cluster takes place: 2NO+ CO + Ti₈O₁₅ → N₂+ Ti₈O₁₆ · CO₂. The proposed model of the reaction agrees well with experimental data.     

Heterospin complexes based on dinuclear CuII triketonate and nitroxides

Heterospin complexes of bis(μ₂-1,1,2,2,8,8,9,9-octafluorononane-3,5,7-trionato)dicopper(II) ([Cu₂L₂]) with nitronyl nitroxides 2-(1-methyl-1H-pyrazol-4-yl)-4,4,5,5-tetramethyl-4,5-dihydro-1H-imidazole-1-oxyl 3-oxide (2) and 4,4,5,5-tetramethyl-2-(3-pyridinyl)-4,5-dihydro-1H-imidazole-1-oxyl 3-oxide (1) were synthesized and structurally characterized. Crystals of the complexes are formed by the discrete bis[1-methyl-4-(4,4,5,5-tetramethyl-3-oxide-1-oxyl-4,5-dihydro-1H-imidazol-2-yl)-1H-pyrazole]-bis (μ₂-1,1,2,2,8,8,9,9-octafluorononane-3,5,7-trionato)dicopper(II) etherate (3) and bis[3-(4,4,5,5-tetramethyl-3-oxide-1-oxyl-4,5-dihydro-1H-imidazol-2-yl)pyridine]-bis (μ₂-1,1,2,2,8,8,9,9-octafluorononane-3,5,7-trionato)dicopper(II) (4) molecules. Each Cu atom of the dinuclear chelate fragment coordinates one paramagnetic ligand through the N atom of the pyrazole or pyridine fragment, respectively. In complex 3, the paramagnetic ligands are located on one side of the plane of the chelate fragment, whereas the ligands in complex 4 are located above and below the plane of the chelate fragment. The magnetic properties of complexes 3 and 4 are determined by dominant antiferromagnetic exchange interactions between the unpaired electrons of the Cu^II atoms in the dinuclear Cu₂L₂ moiety. Dedicated to Academician O. M. Nefedov on the occasion of his 75th birthday. Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 1836–1840, November, 2006.     

Reaction of polyhaloalkyl-substituted chromones, pyrones, and furanones with salicylaldehydes as a direct route to fused 2H-chromenes

Polyhaloalkyl-substituted chromones, gamma-pyrones, and beta-furanones react with salicylaldehydes in the presence of piperidine to give a wide variety of fused 2H-chromenes in good yields. This novel annulation reaction presumably proceeds by a tandem intermolecular oxa-Michael addition and subsequent intramolecular Mannich condensation.     

Determination of selenium and cadmium dopants in nanocomposites based on zinc and indium oxides by high resolution continuous source electrothermal atomic absorption spectrometry and inductively coupled plasma mass spectrometry

An approach is proposed to the determination of selenium and cadmium dopants in new nanocomposites based on zinc and indium oxides. The approach is based on a combination of highly efficient high resolution continuous source electrothermal atomic absorption spectrometry (ETAAS) for the analysis of suspensions and inductively coupled plasma mass spectrometry for the analysis of solutions. A procedure is developed for the determination of Se and Cd dopants and matrix components based on Zn and In in nanocomposite solutions by inductively coupled plasma mass spectrometry. Stabilizing agents for the preparation of suspensions are studied for the ETAAS analysis of powders without their decomposition. The results of determination of CdSe dopants by high resolution ETAAS are validated by inductively coupled plasma mass spectrometry.     

Anomalously interacting new extra vector bosons and their first LHC constraints

In this review phenomenological consequences of the Standard Model extension by means of new spin-1 chiral fields with the internal quantum numbers of the electroweak Higgs doublets are summarized. The prospects for resonance production and detection of the chiral vector Z* and W*^± bosons at the LHC energies are considered on the basis of quantitative simulations within the CompHEP/CalcHEP package. The Z* boson can be observed as a Breit-Wigner resonance peak in the invariant dilepton mass distributions in the same way as the well-known extra gauge Z?? bosons. However, the Z* bosons have unique signatures in transverse momentum, angular and pseudorapidity distributions of the final leptons, which allow one to distinguish them from other heavy neutral resonances. In 2010, with 40 pb^?1 of the LHC proton-proton data at the energy 7 TeV, the ATLAS detector was used to search for narrow resonances in the invariant mass spectrum of e ⁺ e ^? and ??⁺??^? final states and high-mass charged states decaying to a charged lepton and a neutrino. No statistically significant excess above the Standard Model expectation was observed. The exclusion mass limits of 1.15 and 1.35 TeV/c ² were obtained for the chiral neutral Z* and charged W* bosons, respectively. These are the first direct limits on the W* and Z* boson production. Based on the above, a novel strategy for the chiral boson search in the LHC dijet data is discussed. For almost all currently considered exotic models the relevant signal is expected in the central dijet rapidity region y _1,2 ? 0 and |y ₁ ? y ₂| ? 0. On the contrary, the chiral bosons do not contribute to this region but produce an excess of dijet events far away from it. In particular, for these bosons the appropriate kinematical restrictions lead to a dip in the centrality ratio distribution over the dijet invariant mass instead of a bump expected in the most exotic models.     

Unexpected reaction of 1,1,1,10,10,10-hexafluorodecane-2,4,7,9-tetrone with methyl trifluoroacetate

Hexane-2,5-dione or 1,1,1,10,10,10-hexafluorodecane-2,4,7,9-tetrone react with methyl trifluoroacetate in the presence of LiH to give, upon treatment with diluted acid, 6-hydroxy-9-oxo-2,4,10-tris(trifluoromethyl)-3,11,12-trioxatetracyclo[5,2,1,0^2,6,0^4,10]dodecane. The structure of this compound was determined by X-ray diffraction study.     

New Derivatives of 5-Substituted Uracils: Potential Agents with a Wide Spectrum of Biological Activity

Pyrimidine nucleoside analogues are widely used to treat infections caused by the human immunodeficiency virus (HIV) and DNA viruses from the herpes family. It has been shown that 5-substituted uracil derivatives can inhibit HIV-1, herpes family viruses, mycobacteria and other pathogens through various mechanisms. Among the 5-substituted pyrimidine nucleosides, there are not only the classical nucleoside inhibitors of the herpes family viruses, 2′-deoxy-5-iodocytidine and 5-bromovinyl-2′-deoxyuridine, but also derivatives of 1-(benzyl)-5-(phenylamino)uracil, which proved to be non-nucleoside inhibitors of HIV-1 and EBV. It made this modification of nucleoside analogues very promising in connection with the emergence of new viruses and the crisis of drug resistance when the task of creating effective antiviral agents of new types that act on other targets or exhibit activity by other mechanisms is very urgent. In this paper, we present the design, synthesis and primary screening of the biological activity of new nucleoside analogues, namely, 5′-norcarbocyclic derivatives of substituted 5-arylamino- and 5-aryloxyuracils, against RNA viruses.