Back Reaction in Static Einstein Spaces—Change of Entropy

Using the thermodynamical approach and the method of York, the back-reaction of anti-de Sitter Schwarzschild black hole in thermal equilibrium with conformal spin-2 field is studied. It is found that both approaches give identical results.     

Thermal analysis and kinetics of the copper-lead matte roasting process

In this paper, the results of copper-lead matte investigations are presented. Investigated copper-lead matte is intermediate product of the lead production in TREPCA-Zvečan. In the first part of the paper characterization of starting material is presented, consisting of: chemical composition analysis (XRQ), scanning electron microscopy (SEM) and diffractometry (XRD). Thermal properties of investigated matte were determined using differential thermal analysis (DTA) at characteristic temperatures. Using results of induced analysis, mechanism of matte oxidation process was determined. In the second part of the paper kinetic parameters describing oxidative roasting of copper-lead matte are presented. For activation energy calculations, non-isothermal methods defined by Kissinger and Ozawa were used [1, 2]. Kinetic equation describing oxidation process was determined using Sharps method of reduced half time of reaction [3].     

Mechanistic studies of the addition of carbonyl compounds to tetramesityldigermene

The mechanism of the addition of carbonyl compounds to digermenes was investigated by examining the reaction between tetramesityldigermene and two mechanistic probes: trans-2-phenylcyclopropane carbaldehyde and trans,trans-2-methoxy-3-phenylcyclopropane carbaldehyde. In each reaction, two diastereomers of the formal [2+2] cycloadduct between the aldehyde and the digermene were obtained. These findings, together with the results of a recent theoretical study, indicate that the addition of carbonyl compounds to digermenes proceeds via a mechanism involving a zwitterionic intermediate.     

Isometric graphing and multidimensional scaling for reaction-diffusion modeling on regular and fractal surfaces with spatiotemporal pattern recognition

Heterogeneous surface reactions exhibiting complex spatiotemporal dynamics and patterns can be studied as processes involving reaction-diffusion mechanisms. In many realistic situations, the surface has fractal characteristics. This situation is studied by isometric graphing and multidimensional scaling (IGMDS) of fractal surfaces for extracting geodesic distances (i.e., shortest scaled distances that obtain edges of neighboring surface nodes and their interconnections) and the results obtained used to model effects of surface diffusion with nonlinear reactions. Further analysis of evolved spatiotemporal patterns may be carried out by IGMDS because high-dimensional snapshot data can be efficiently projected to a transformed subspace with reduced dimensions. Validation of the IGMDS methodology is carried out by comparing results with reduction capabilities of conventional principal component analysis for simple situations of reaction and diffusion on surfaces. The usefulness of the IGMDS methodology is shown for analysis of complex patterns formed on both regular and fractal surfaces, and using generic nonlinear reaction-diffusion systems following FitzHugh Nagumo and cubic reaction kinetics. The studies of these systems with nonlinear kinetics and noise show that effects of surface disorder due to fractality can become very relevant. The relevance is shown by studying properties of dynamical invariants in IGMDS component space, viz., the Lyapunov exponents and the KS entropy for interesting situations of spiral formation and turbulent patterns.     

Developments of Asymmetric Synthesis Mediated by Chiral Sulfur Reagents

Abstract

Our work on the thio-Claisen rearrangement mediated by an adjacent sulfinyl group is reviewed. The substrates could easily be prepared on a large scale from diacetone-D-glucose. The rearrangement was effected with a diastereoselectivity of 95:5, in favor of the (S,S) or the (R,R) isomer. An approach to natural bis(lactones) was investigated, using a halolactonization reaction and a second [3,3] sigmatropic shift, again mediated by the sulfinyl group. The second part deals with the catalytic enantioselective benzylidenation of aldehydes, mediated by chiral sulfur ylides. We have introduced simple C ₂ symmetric thiolanes for that purpose. The procedure is very practical and enantiomeric excesses up to 96% have been reported for the model of stilbene oxide. A series of ferrocenyl sulfides with planar chirality has also been investigated, leading to unexpected diastereoselectivities and enantiomeric excesses up to 94%.     

Calorimetric study and thermal analysis of Al–Sn system

The results of calorimetric study and thermal analysis of binary Al–Sn system are presented in this paper. The Oelsen calorimetry was used in thermodynamic analysis. Following thermodynamic properties were determined at 727 °C: activities, activity coefficients, partial/integral molar Gibbs excess, and mixing energies. The energetics of mixing in liquid Al–Sn alloys has been analyzed through the study of concentration fluctuation in the long-wavelength limit. Thermal analysis of selected alloys in Al–Sn system was done using differential thermal analysis. Defined characteristic phase transition temperatures were used for comparison with calculated phase diagram of investigated system. Good agreement with available literature data was obtained. Structural analysis of selected alloys was done using optic microscopy.     

A new phenanthroindolizidine alkaloid from Tylophora indica

A new phenanthroindolizidine alkaloid, 3-O-demethyl tylophorinidine (VI), was isolated from the aerial (leaves and stem) parts of Tylophora indica and characterized using different spectral techniques. Gel chromatography and reverse phase preparative HPLC were used for sample purification. The new alkaloid, VI, was screened for anticancer activity against a panel of different cancer cell lines and it showed significant anticancer activity with IC₅₀ value in the range of 0.89?C1.40 ??M.     

Magnetic field rectifiers using semicircular Josephson junctions

A novel method for rectifying alternating magnetic fields is demonstrated using fluxons in semicircular Josephson junctions. An external magnetic field applied parallel to the dielectric barrier of the semicircular junction has opposite polarities at the ends of the junction and supports penetration of opposite polarity fluxons into the junction in the presence of a constant dc bias. When the direction of the field is reversed, flux penetration is not possible and a flux-free state exists in the junction. Thus, effective rectification of an alternating magnetic field can be achieved in semicircular Josephson junctions. This unique phenomenon is specific to this geometry and can be employed in rf SQUID magnetometers.