Effects of oscillatory shear flow on chain-like cluster dynamics in ferrofluids without magnetic fields

Brownian dynamics simulations of interacting magnetic particles in a quasi-two-dimensional ferrofluid system are performed at zero temperature, under the influence of oscillatory shear flow in the absence of external magnetic fields. Starting from chain-like clusters of the particles, we study the time-dependent behavior of both magnetization and microstructures of the ferrofluid by changing values of two parameters, the shear rate strength and frequency of oscillatory shear flow. Simulation results show that there are three different dynamical regimes for the chain clusters dynamics, depending on these two parameters. Scaling behavior of the asymptotic magnetization is also observed for a certain range of parameters.     

Precision measurement of neutrino oscillation parameters with KamLAND

The KamLAND experiment has determined a precise value for the neutrino oscillation parameter Deltam21(2) and stringent constraints on theta12. The exposure to nuclear reactor antineutrinos is increased almost fourfold over previous results to 2.44 x 10(32) proton yr due to longer livetime and an enlarged fiducial volume. An undistorted reactor nu[over]e energy spectrum is now rejected at >5sigma. Analysis of the reactor spectrum above the inverse beta decay energy threshold, and including geoneutrinos, gives a best fit at Deltam21(2)=7.58(-0.13)(+0.14)(stat) -0.15+0.15(syst) x 10(-5) eV2 and tan2theta12=0.56(-0.07)+0.10(stat) -0.06+0.10(syst). Local Deltachi2 minima at higher and lower Deltam21(2) are disfavored at >4sigma. Combining with solar neutrino data, we obtain Deltam21(2)=7.59(-0.21)+0.21 x 10(-5) eV2 and tan2theta12=0.47(-0.05)+0.06.     

Hyperfine-structure-induced purely long-range molecules

We have experimentally observed and theoretically identified a novel class of purely long-range molecules. This novel purely long-range state is formed due to a very weak hyperfine interaction that is usually treated only as a small perturbation in molecular spectra. Photoassociation spectroscopy of ultracold ytterbium (171Yb) atoms with the 1S0-3P1 intercombination transition presents clear identification of molecular states and the shallowest molecular potential depth of about 750 MHz among the purely long-range molecules ever observed.     

ChemInform Abstract: Determination of the Space Group of LaCrO3 by Convergent‐Beam Electron Diffraction.

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.     

Deciphering the Biological Activities of Antifungal Agents with Chemical Probes

The growing number of fungal infections caused by pathogens resistant to one or more classes of antifungal drugs emphasizes the threat that these microorganisms pose to animal and human health and global food security. Open questions remain regarding the mechanisms of action of the limited repertoire of antifungal agents, making it challenging to rationally develop more efficacious therapeutics. In recent years, the use of chemical biology approaches has resolved some of these questions and has provided new promising concepts to guide the design of antifungal agents. By focusing on examples from studies carried out in recent years, this minireview describes the key roles that probes based on antifungal agents and their derivatives have played in uncovering details about their activities, in detecting resistance, and in characterizing the interactions between these agents and their targets.     

Dimensionally oriented redox-active π-conjugated systems

Porphyrins bearing the redox-active phenylenediamine pendant groups are synthesized to afford dimensionally oriented π-conjugated systems. The structural and electronic characteristics depend on the atropisomers. In the fluorescence emission spectra, the emission from the porphyrin moiety is almost completely quenched. Zinc complexation of the αααα isomers gives the corresponding zinc porphyrins bearing four phenylenediamine strands. Treatment with a bidentate ligand, DABCO, leads to the sandwich dimer complex, in which the porphyrin moieties are surrounded by π-conjugated pendant groups. p-t-Butylcalix[4]arenes bearing four redox-active phenylenediamine pendant groups on the lower rim are synthesized and characterized both spectroscopically and electrochemically. The interconversion of the oxidation states of the pendant groups is demonstrated both chemically and electrochemically.