Real-time monitoring of the origination of multimacroion domains in a polyelectrolyte solution

First real-time monitoring of the origination of multimacroion domains in an initially homogeneous polyelectrolyte solution was performed. Domains were generated by pH-induced increase of macroion charge in solution of poly(methacrylic acid). Monitoring was performed by static and dynamic light scatterings, in which scattering contributions from individual polyions and growing multimacroion domains were separated, such that amplitudes of both modes were expressed in absolute units. Kinetic results also yield new information regarding the nature of multimacroion domains.     

Percolation and epidemic thresholds in clustered networks

We develop a theoretical approach to percolation in random clustered networks. We find that, although clustering in scale-free networks can strongly affect some percolation properties, such as the size and the resilience of the giant connected component, it cannot restore a finite percolation threshold. In turn, this implies the absence of an epidemic threshold in this class of networks, thus extending this result to a wide variety of real scale-free networks which shows a high level of transitivity. Our findings are in good agreement with numerical simulations.     

Bioactive eremophilanolides from Senecio poepigii

A new bioactive eremophilanolide, 1alpha-tigloyloxy-8betaH,10betaH-eremophil-7(11)-en-8alpha,12-olide, was isolated from Senecio poepigii and its structure was elucidated by spectral analysis. 1alpha-Angeloyloxy-8beta-methoxy-10betaH-eremophil-7(11)-en-8alpha,12-olide was also isolated. Antifungal and insect antifeedant properties were evaluated.     

Tetrapyrrole singlet excited state quenching by carotenoids in an artificial photosynthetic antenna

Two artificial photosynthetic antenna models consisting of a Si phthalocyanine (Pc) bearing two axially attached carotenoid moieties having either 9 or 10 conjugated double bonds are used to illustrate some of the function of carotenoids in photosynthetic membranes. Both models studied in toluene, methyltetrahydrofuran, and benzonitrile exhibited charge separated states of the type C*+-Pc*- confirming that the quenching of the Pc S1 state is due to photoinduced electron transfer. In hexane, the Pc S1 state of the 10 double bond carotenoid-Pc model was slightly quenched but the C*+-Pc*- transient was not spectroscopically detected. A semiclassical analysis of the data in hexane at temperatures ranging from 180 to 320 K was used to demonstrate that photoinduced electron transfer could occur. The model bearing the 10 double bond carotenoids exhibits biexponential fluorescence decay in toluene and in hexane, which is interpreted in terms of an equilibrium mixture of two isomers comprising s-cis and s-trans conformers of the carotenoid. The shorter fluorescence lifetime is associated with an s-cis carotenoid conformer where the close approach between the donor and acceptor moieties provides through-space electronic coupling in addition to the through-bond component.     

Asymptotic quadratic convergence of the parallel block-Jacobi EVD algorithm with dynamic ordering for Hermitian matrices

The proof of the asymptotic quadratic convergence is provided for the parallel two-sided block-Jacobi EVD algorithm with dynamic ordering for Hermitian matrices. The discussion covers the case of well-separated eigenvalues as well as clusters of eigenvalues. Having p processors, each parallel iteration step consists of zeroing 2p off-diagonal blocks chosen by dynamic ordering with the aim to maximize the decrease of the off-diagonal Frobenius norm. Numerical experiments illustrate and confirm the developed theory.     

Groups satisfying weak chain conditions on non-modular subgroups

In this paper (generalized) soluble groups for which the set of all non-modular subgroups satisfies some weak chain condition are described. Groups satisfying weak chain conditions on non-permutable subgroups are also considered.     

Large-scale supramolecular structure in solutions of low molar mass compounds and mixtures of liquids: II. Kinetics of the formation and long-time stability

Kinetics of the formation of large-scale supramolecular structure and its long-time stability were investigated in detail in solutions of electrolytes, nonelectrolytes, and mixtures of liquids. This structure comprises submicron-sized domains (large clusters) with higher solute concentration than in the rest of solution. In the case of mixtures of liquids, a complete real-time monitoring of the structure formation was possible in all cases. In the case of solutions of solid samples, the observation was possible in cases when the structure formation was significantly slower than the dissolution process. The time scale on which the supramolecular structure develops varies from minutes to weeks, depending on the concrete system. The long-time stability of the developed structure was investigated in time intervals ranging up to 15 months. In some systems the resulting domain structure appears stable, in others a very slow ceasing of domains is observed over very long time intervals. In all cases, however, slow kinetic effects are present in the systems investigated. Among others, data on some common substances of great chemical and biological importance such as sodium chloride, acetic acid, glucose, and ethanol, are presented.