EXTENSION OF MULTIPLIERS AND INJECTIVE HILBERT MODULES

The author studies the problem whether a multiplier of a hereditary C^*-subalgebra B of a C^*-algebra A can be extended to a multiplier of A. One related problem is the Hahn-Banach extension theorem for Hilbert modules over C^*-algebras. It is shown that every self-dual Hilbert module over W^*-algebra or an injective C^*-algebra is injective.     

关于三商映射

三商映射是完备映射和开映射的共同推广。本文综述三商映射的理论，论术这三商映射，开映射，紧覆盖映射，诱导完备映之间的一些转换关系，提出了几个供进一步研究的问题。     

第I类非自共轭锥上的Gamma函数

本文将Ｇａｍｍａ函数及Ｓｉｅｇｅｌ积分推广到一般的第Ｉ类非自共轭锥上．作为其应用，显式给出了以这些锥为底的管状域（或第一类Ｓｉｅｇｅｌ域）的Ｃａｕｃｈｙ Ｓｚｅｇ¨ｏ核和形式Ｐｏｉｓｏｎ核．     

HoYb:YVO4的上转换发光研究

研究了960nm激光激发下HoYb双掺钒酸钇晶体HoYb:YVO4的直接上转换增敏发光,发现了Ho3+离子的上转换发光现象,HoYb:YVO4晶体的上转换发光是5F5→5I8最强,而5S2→5I8相对小了一个数量级,这是由于YVO4晶体既有很强的振子强度又有很大的多声子无辐射弛豫造成的. 关键词： 上转换发光 直接增敏(敏化) 钒酸钇YVO4晶体 Ho3+离子     

Substitution Reaction of Tetracyanoethylene with Acetone-Anils

The products from the condensation of acetone-anils ( 1 ) and TCNE reaction were characterized after separation. The main products, tricyanoethylene derivatives ( 7–9 ) were isolated with the malonodinitrile derivatives ( 10–12 ), respectively. The [2+2] cycloaddition product ( 13 ), namely 5-methoxy-3,4-(2′,2′,3′,3′-tetracyanocyclobutano)-l,2-dihydro-2,2,4-trimethylquinoline also has been isolated. The distribution of these three products is substituent dependent.     

Bio-Plasmonics: Nano/micro Structure of Surface Plasmon Resonance Devices for Biomedicine

We have reported a novel design of surface plasmon resonance (SPR) device, which uses alternating dielectric layers to enhance the SPR signal quality and modulate its resonant position. Admittance loci method of thin film design has been used in the design of such a device. The use of biomolecular thin film, such as DNAs or Porteins, in this design can result in resonant condition of wavelength changes as well. Bio-plasmonics is proposed for the research and development of novel devices, which use biomolecules as a part of the plasmon oscillation system to actively interact with nano/micro structure.     

Actively mode-locked dual-wavelength fiber laser with close wavelength spacing using a fiber Bragg grating

A simple actively mode-locked fiber ring laser is proposed and successfully demonstrated to generate dual-wavelength picosecond pulses with close wavelength spacing using one Bragg grating in standard single-mode fiber. The proposed laser can be made to operate in stable dual-wavelength at room temperature, due to the birefringence characteristic of the FBG induced by transverse strain. Transverse strain loading on the FBG allows the wavelength spacing to be controlled. Generation of stable dual-wavelength pulses with a pulsewidth of 212–234 ps and a tunable wavelength separation from 0.2 to 0.44 nm at a pulse rate of 1.05 GHz was demonstrated.     

Crystal structure and magnetic properties of two new cobalt selenite halides: Co5(SeO3)4X2 (X=Cl, Br)

Two new isostructural cobalt selenite halides Co₅(SeO₃)₄Cl₂ and Co₅(SeO₃)₄Br₂ have been synthesized. They crystallize in the triclinic system space group P−1 with the following lattice parameters for Co₅(SeO₃)₄Cl₂: a=6.4935(8) Å, b=7.7288(8) Å, c=7.7443(10) Å, α=66.051(11)°, β=73.610(11)°, γ=81.268(9)°, and Z=1. The crystal structures were solved from single-crystal X-ray data, R1=3.73 and 4.03 for Co₅(SeO₃)₄Cl₂ and Co₅(SeO₃)₄Br₂, respectively. The new compounds are isostructural to Ni₅(SeO₃)₄Br₂.Magnetic susceptibility measurements on oriented single-crystalline samples show anisotropic response in a broad temperature range. The anisotropic susceptibility is quantitatively interpreted within the zero-field splitting schemes for Co²⁺ and Ni²⁺ ions. Sharp low-temperature susceptibility features, at T_N=18 and 20 K for Co₅(SeO₃)₄Cl₂ and Co₅(SeO₃)₄Br₂, respectively, are ascribed to antiferromagnetic ordering in a minority magnetic subsystem. In isostructural Ni₅(SeO₃)₄Br₂ magnetically ordered subsystem represents a majority fraction (T_N=46 K). Nevertheless, anisotropic susceptibility of Ni₅(SeO₃)₄Br₂ is dominated at low temperatures by a minority fraction, subject to single-ion anisotropy effects and increasing population of S_z=0 (singlet) ground state of octahedrally coordinated Ni²⁺.