Suppression of MeIQ-induced SOS response by allylbenzenes from Asiasarum heterotropoides in the Salmonella typhimurium OY1001/1A2 umu test

Three allylbenzenes from Asiasarum heterotropoides, methyleugenol (1), elemicin (2) and gamma-asaron (3) showed suppressive effects on umu gene expression of the SOS response in the Salmonella typhimurium OY1001/1A2 umu test against the mutagen 2-amino-3,4-dimethylimidazo[4,5-f ]quinoline (MeIQ). Gene expression was suppressed 70.0, 75.9 and 81.7% at a concentration of 0.4 mM, respectively. The ID50 values (50% inhibition dose) of these compounds were 0.125, 0.098 and 0.059 mM, respectively. On the other hand, compounds 1-3 showed weak suppressive effects of the SOS-inducing activity on activated MeIQ.     

Symmetry properties of three-dimensional magnetization distributions induced by focused circularly polarized lights

We analyze symmetry properties of the three-dimensional magnetization distribution in the optic-magneto film induced by focused circularly polarized lights. The magnetization distributions are derived and evaluated based on the vector diffraction theory and the inverse Faraday effect of the isotropic and nonmagnetically ordered material. It is shown that for any radial symmetrical amplitude, phase, or hybrid amplitude-phase pupil filter, the magnetization distribution of the axial component is circular symmetric but those of the radial and azimuthal components are annular symmetric with regard to the optical axis. All of the three components have a symmetric distribution with regard to the focal plane. The direction of both axial and radial components can be inversed with the helicity of incident circularly polarized light but the direction of azimuthal component is independent of helicity. The axial component has a decisive effect to all-optical magnetic recording, and within the effective axial range, the size of its magnetization domain hardly expands in the transverse direction.     

Ferromagnetic Intermolecular Interaction of N-Protonated Pyridylphenylcarbene

Abstract

The HCl and DCl salts of pheny1-4-pyridyldiazomethane were prepared and irradiated at 6 K to generate the carbenes. Their ESR spectra indicated presence of plural triplet carbenes with slightly-different zero-field splitting constants. Besides the triplet species, we found a quintet species whose signal intensity decreases with increasing temperature. The quintet spin state was concluded to be a ground state which was produced by an intermolecular ferromagnetic interaction of the triplet carbenes. The ferromagnetic interaction would be explained by the McConnell mechanism, judging from the crystal structure of the HCl salt of phenyl-4-pyridylketone.     

Sonochemical degradation of chlorophenols in water

Sonochemical degradation of dilute aqueous solutions of 2-, 3- and 4-chlorophenol and pentachlorophenol has been investigated under air or argon atmosphere. The degradation follows first-order kinetics in the initial state with rates in the range 4.5-6.6 microM min-1 under air and 6.0-7.2 microM min-1 under argon at a concentration of 100 microM of chlorophenols. The rate of OH radical formation from water is 19.8 microM min-1 under argon and 14.7 microM min-1 under air in the same sonolysis conditions. The sonolysis of chlorophenols is effectively inhibited, but not completely, by the addition of t-BuOH, which is known to be an efficient OH radical scavenger in aqueous sonolysis. This suggests that the main degradation of chlorophenols proceeds via reaction with OH radicals; a thermal reaction also occurs, although its contribution is small. The addition of appropriate amounts of Fe(II) ions accelerates the degradation. This is probably due to the regeneration of OH radicals from hydrogen peroxide, which would be formed from recombination of OH radicals and which may contribute a little to the degradation. The ability to inhibit bacterial multiplication of pentachlorophenol decreases with ultrasonic irradiation.     

New opportunities offered by compact sub‐nanosecond supercontinuum sources in ultra‐broadband multiplex CARS microspectroscopy

We report, to the best of our knowledge, the first turn‐key and compact dual‐output sub‐nanosecond supercontinuum source applicable to ultrabroadband multiplex coherent anti‐Stokes Raman scattering microspectroscopy of biological samples. The light source design and the microspectroscopy setup are described in details. Easy multicolour imaging of Caenorhabditis elegans nematode is operated successfully and discussed. Copyright © 2011 John Wiley & Sons, Ltd.     

N=8 Armchair Graphene Nanoribbons: Solution Synthesis and High Charge Carrier Mobility**

Structurally defined graphene nanoribbons (GNRs) have emerged as promising candidates for nanoelectronic devices. Low band gap (<1 eV) GNRs are particularly important when considering the Schottky barrier in device performance. Here, we demonstrate the first solution synthesis of 8-AGNRs through a carefully designed arylated polynaphthalene precursor. The efficiency of the oxidative cyclodehydrogenation of the tailor-made polymer precursor into 8-AGNRs was validated by FT-IR, Raman, and UV/Vis-near-infrared (NIR) absorption spectroscopy, and further supported by the synthesis of naphtho[1,2,3,4-ghi]perylene derivatives ( 1 and 2 ) as subunits of 8-AGNR , with a width of 0.86 nm as suggested by the X-ray single crystal analysis. Low-temperature scanning tunneling microscopy (STM) and solid-state NMR analyses provided further structural support for 8-AGNR . The resulting 8-AGNR exhibited a remarkable NIR absorption extending up to ∼2400 nm, corresponding to an optical band gap as low as ∼0.52 eV. Moreover, optical-pump TeraHertz-probe spectroscopy revealed charge-carrier mobility in the dc limit of ∼270 cm² V⁻¹ s⁻¹ for the 8-AGNR .     

Pressure effect to chemical reaction,hydrogen isotope recombination reactions in liquid helium at cryogenic temperature — Part II

Behavior of the hydrogen isotope in recombination reactions, H+H→H₂ H+T→HT and T+T→T₂ under pressurized conditions at 1.6 K were investigated using liquid helium as cryogenic reaction media by radiochemical methods. Pressure effects were observed in changes of isotope ratio HT/T₂. It became clearer that the balance of changes in bubble energy effective mass associated with energy and chemical potential contributed to the recombination reactions through bubble states. It was suggested that bubble radius was decreased significantly at higher pressure.     

Universal character and <Emphasis Type="Italic">q</Emphasis>-difference Painlevé equations

The universal character is a polynomial attached to a pair of partitions and is a generalization of the Schur polynomial. In this paper, we introduce an integrable system of q-difference lattice equations satisfied by the universal character, and call it the lattice q-UC hierarchy. We regard it as generalizing both q-KP and q-UC hierarchies. Suitable similarity and periodic reductions of the hierarchy yield the q-difference Painlevé equations of types , , and . As its consequence, a class of algebraic solutions of the q-Painlevé equations is rapidly obtained by means of the universal character. In particular, we demonstrate explicitly the reduction procedure for the case of type via the framework of τ based on the geometry of certain rational surfaces.     

Enantioselective hydrogenation of aromatic ketones catalyzed by Ru complexes of Goodwin-Lions-type sp2N/sp3N hybrid ligands R-BINAN-R'-Py

Goodwin-Lions-type sp2N/sp3N hybrid ligands R-BINAN-R'-Py possessing a C2 axis binaphthyl skeleton have been designed and synthesized. Combination of the new non-phosphine ligand with Ru(pi-CH2C(CH3)CH2)2(cod) has been revealed to catalyze the hydrogenation of aromatic ketones with high enantioselectivity of up to 99% ee. The reaction proceeds essentially without the need for any bases, but the reactivity is enhanced by the addition of KOt-C4H9 attaining an S/C ratio of up to 10 000. The success should expand the range of possibilities in designing catalysts not only for hydrogenation but also for many other reactions.