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.     

Unveiling Latent Photoreactivity of Imines

Unlike carbonyl compounds, it has long been common understanding that excited imines show virtually no photoreactivity, and hence their properties and potential utility in chemical science remain largely unexplored. Now, a strategy is presented for eliciting latent photoreactivity of imines based on the introduction of a donor–acceptor (D‐A) structure to extend the lifetime of their photoexcited states. A series of spectroscopic analyses and density functional theory calculations reveal unique photophysical properties of the D‐A‐type imines. Furthermore, the reactivity of the D‐A‐type imines is demonstrated by using them as a photoredox catalyst for atom‐transfer radical addition. These findings illuminate a previously neglected chemical space in the field of photochemistry, which will be exploited by taking advantage of the inherent structural modularity of imines.     

Dynamically reconfigurable characteristics of a double phase conjugate mirror using Sn2P2S6 crystals and their application to optical inter-satellite communication

A double phase conjugate mirror (DPCM), created by two mutually incoherent beams entering photorefractive nonlinear materials, can generate a phase conjugate beam whose reflectivity may be greater than 100%. Even though the conditions of the incident beams are changed, the DPCM can be dynamically reconfigured by using a Sn₂P₂S₆ crystal with a high response speed. These features of the DPCM are advantageous, particularly in an optical inter-satellite communication system. In particular, use of the phase conjugate beam from the DPCM offers wavefront compensation and amplification in satellite communication. In addition, the dynamically reconfigurable DPCM using a Sn₂P₂S₆ crystal relaxes the acquisition accuracy of the signal beam in the system. In this study, the temporal and spatial operating characteristics of the DPCM using a Sn2P2S6 crystal were first clarified. Next, an inter-satellite system based on the DPCM was proposed, and it was demonstrated that our system significantly improves the tolerance of the acquisition accuracy and tracking time.     

Facile synthesis of picene from 1,2-di(1-naphthyl)ethane by 9-fluorenone-sensitized photolysis

A facile formation of picene was achieved by photosensitization of 1,2-di(1-naphthyl)ethane using 9-fluorenone as a sensitizer. This sensitized photoreaction is the first photochemical cyclization of ethylene-bridged naphthalene moieties to afford the picene skeleton. 5,8-Dibromopicene, prepared by this procedure using 1,2-di[1-(4-bromonaphthyl)]ethane as the substrate, was readily converted to novel functionalized picenes by conventional substitution and cross-coupling reactions.     

Biliary excretion of essential trace elements in rats under oxidative stress caused by selenium deficiency

The excretion of essential trace elements, namely, Se, Sr, As, Mn, Co, V, Fe, and Zn into the bile of Se-deficient (SeD) Wistar male rats was studied using the multitracer (MT) technique, and instrumental neutron activation analysis (INAA). Normal and Se-control (SeC) rat groups were used as reference groups to compare the effects of Se levels on the behaviors of the essential trace elements. The excretion (% dose) of Se, Sr, As, Mn, Co, and V increased with Se levels in the liver. The biliary excretion of Mn and As dramatically enhanced for SeC rats compared with SeD rats, while that of V accelerated a little for SeC rats. The radioactivity levels of ⁵⁹Fe and ⁶⁵Zn in the MT tracer solution were insufficient to measure their excretion into bile. The role of glutathione and bilirubin for biliary excretion of the metals was discussed in relation to Se levels in rat liver.     

Higher-order correlated calculations based on fragment molecular orbital scheme

We have developed a new module for higher-order correlated methods up to coupled-cluster singles and doubles with perturbative triples (CCSD(T)). The matrix-matrix operations through the DGEMM routine were pursued for a number of contractions. This code was then incorporated into the ABINIT-MPX program for the fragment molecular orbital (FMO) calculations. Intra-fragment processings were parallelized with OpenMP in a node-wise fashion, whereas the message passing interface (MPI) was used for the fragment-wise parallelization over nodes. Our new implementation made the FMO-based higher-order calculations applicable to realistic proteins. We have performed several benchmark tests on the Earth Simulator (ES2), a massively parallel computer. For example, the FMO-CCSD(T)/6-31G job for the HIV-1 protease (198 amino acid residues)?Clopinavir complex was completed in 9.8?h with 512 processors (or 64 nodes). Another example was the influenza neuraminidase (386 residues) with oseltamivir calculated at the full fourth-order M?ller?CPlesset perturbation level (MP4), of which job timing was 10.3?h with 1024 processors. The applicability of the methods to commodity cluster computers was tested as well.