Quantum deformedsu(m/n) algebra and superconformal algebra on quantum superspace

We study a deformedsu(m/n) algebra on a quantum superspace. Some interesting aspects of the deformed algebra are shown. As an application of the deformed algebra we construct a deformed superconformal algebra. From the deformedsu(1/4) algebra, we derive deformed Lorentz, translation of Minkowski space,iso(2, 2) and its supersymmetric algebras as closed subalgebras with consistent automorphisms.     

E 6,7,8 magnetized extra-dimensional models

We study 10D super Yang–Mills theory with the gauge groups E ₆, E ₇ and E ₈. We consider the torus/orbifold compactification with magnetic fluxes and Wilson lines. They lead to 4D interesting models with three families of quarks and leptons, whose profiles in extra dimensions are quasi-localized because of magnetic fluxes.     

Assignment of dielectric loss of K-L zeolite

Dielectric spectra of zeolite L (LTL) with potassium ions were measured to investigate movements of potassium ion in it. K,TMA-L was prepared through an ion-exchange of K9-L with tetramethylammonium (TMA) ion, and changed to K,H-L by gentle calcination in air. Since the TMA ion in K,TMA-L was expected to exclusively occupy site D, the hydrogen ion in K,H-L was considered to be located around site D. K9-xHx-L with 0相似文献   

Solvent effect on the photochemical properties of symmetrically substituted trans-3,3',5,5'-tetramethoxystilbene

Photochemical properties of trans-3,3',5,5'-tetramethoxystilbene (TMST) have been studied in various polar solvents. The Stokes shift of trans-TMST was found to be increased with increasing solvent polarity. The fluorescence lifetime of trans-TMST experienced a large solvent effect changing from 2.3 ns in cyclohexane to 16.6 ns in acetonitrile. These results indicate that the excited singlet state of trans-TMST has a charge-transfer (CT) character. On the basis of the obtained results, the interior polar environment of a water-soluble TMST dendrimer is discussed.     

Band engineering of silicon for light emission: First-principles approach to the effect of co-doping with nitrogen and fluorine

A Si-based light emitter has long been the final key component for electronic and photonic integrated circuits on Si, because Si has an indirect band gap. Atomistic and electronic structures and energy gains of formation of possible nitrogen (N) and fluorine (F) complexes in Si have been researched from first-principles, in order to engineer the band structure of Si for light emission. The calculated results show that the substitutional nitrogen N_S and bond center fluorine F_BC pair complex has large stabilization energy, and that the pair-complex-doped Si has direct band gap, which is reduced with respect to that of Si. These results lead to the possibilities of doping-based engineering of Si optical properties with introduction of deep-level impurity and charge compensation.     

Macroporous Oxide Platforms Templated by Non‐Close‐Packed Spherical Copolymer Aggregates

Exclusive organic templating of macroporous oxide films is reported by using non‐close and lose packing of spherical copolymer aggregates, in combination with facile control of condensation degree/density of inorganic oxide frameworks. Unique macroporous oxide films, mainly titania showing highly porous, crystalline, and versatile properties, can be fabricated with continuous design from unusual 3‐D net‐shape to tunable spherical macrostructures, which expands the preparation of other inorganic oxide films (silica, alumina, and zirconia) and possibly adapts the use of other assembled organic polymers. The macroporous structures are helpful for effective accommodation of bulky biomoleculeshigh and diffusivity of organic molecules (useful for photocatalysts). Unusual structural variation, expansion of spherical voids, is also observed, being useful for fine tuning of optical property.     

Facile Synthesis of Free‐Standing Polymer Brush Films Based on a Colorless Polydopamine Thin Layer

A free‐standing polymer brush film with tailored thicknesses based on a colorless polydopamine (PDA) thin layer is prepared and characterized. The surface‐initiated atom transfer radical polymerization (ATRP) of 2‐hydroxyethyl methacrylate (HEMA) is performed on a PDA layer with thickness of ca. 6 nm, which generated an optically transparent and colorless free‐standing PHEMA brush film (1.5 cm × 1.5 cm). Because the cross‐linked PDA layer is used as the base for the polymer brushes, the reported method does not require cross‐linking the polymer brushes. The free‐standing film thicknesses of ≈16–75 nm are controlled by simply changing the ATRP reaction time. The results show that the free‐standing PHEMA brush film transferred onto a plate exhibits a relatively smooth surface and is stable in any solvent.

     

Fluorescence detected circular dichroism of a red-shifted exciton-coupling chromophore <Emphasis Type="Italic">N</Emphasis>,<Emphasis Type="Italic">N</Emphasis>′-carbonyl-bridged dipyrrinone derivative using an ellipsoidal device

A fluorescent red-shifted exciton-coupling chromophore, N,N′-carbonyl-bridged dipyrrinone, was subjected to fluorescence-detected CD (FDCD) measurements as a primitive structure-elucidating probe with trans-1,2-cyclohexanediol template in several solvents under various instrumental conditions. With the help of a JASCO ellipsoidal mirror device FDCD465, a chloroform solution achieved the sensitivity enhancement by 50 times of the transmission CD and 5 times of the conventional FDCD. All FDCD spectra were completely free from the polarization artifacts. Correspondence: Tatsuo Nehira and David A. Lightner, Graduate School of Integrated Arts and Sciences, Hiroshima University, Higashi-hiroshima 739-8521, Japan; Department of Chemistry, University of Nevada, Reno, Nevada 89557, USA.