Inactivation of bovine immunodeficiency virus by photodynamic therapy with HMME

To investigate the effect of photodynamic therapy (PDT) with hematoporphrin monomethyl ether (HMME) on bovine immunodeficiency virus (BIV) can provide the basis theory for photoinactivation of human immunodeficiency virus (HIV). To assess the protection of HMME-PDT on the cell line Cf2Th infected with BIVR29 by 3-(4,5)-dimethylthiahiazol-2-yl-3,5-di-phenytetrazolium bromide (MTT) with power density of 5 and 25 mW/cm2 and energy density from 0.6 to 3 J/cm<'2>. To observe the inhibition of membrane fusion using a new reporter cell line BIVE by fluorescence microscope. HMME-PDT has significant protectant effects on Cf2Th-BIVR29 with both power densities, especially in the group of high power density. Fluorescent microscope shows that there is no significant difference between the group of PDT and control, which means PDT could not inhibit the BIV-mediated membrane fusion.     

Influence of the KTP crystal boundary temperature on conversion efficiency in high power green laser

The influence of the KTiOPO4 (KTP) crystal boundary temperature on conversion efficiency in high power green laser has been studied theoretically and experimentally. Temperature distribution inside the KTP crystal has been analyzed by solving the thermal conductivity equation. From the temperature distribution inside the KTP crystal, we have calculated the optimal phase-matching angles of the type-Ⅱ KTP crystal as a function of temperature. The second-harmonic conversion efficiency as a function of temperature has also been calculated. In the experiment, two KTP crystals with different phase-matching angles were used in the intrcavity-frequency-doubled resonator. When the boundary temperature of KTP-A (φ = 23.6°,θ = 90° under the condition of 27 ℃ temperature) was setting at 4 ℃, a maximum green light power of 104 W was generated at repetition rate of 20.7 kHz and pulse width of 132 nm with pumping current of laser diode of 18.3 A, leading to 10.2% optical-to-optical conversion efficiency. When KTP-B crystal (φ = 24.68°, θ = 90° under the condition of 80 ℃ temperature) was employed, an average output power of 110 W at 532 nm has been achieved with values of 11.5% and 2% for the optical-to-optical efficiency and the instability, respectively. The optimal boundary temperature of this KTP crystal has been found to be 48.8 ℃.     

扩链法合成聚乳酸类生物降解材料

详细地综述了聚乳酸类生物降解材料的扩链法合成，特别是使用二异氰酸酯类、二恶唑淋类扩链剂的合成进展。参考文献37篇。     

Preparation and properties of siloxane liquid crystalline elastomers with a mesogenic crosslinking agent

A mesogenic crosslinking agent M-1 was synthesized to minimize the perturbations of non-mesogenic crosslinking agents in liquid crystalline elastomers. The synthesis of new side chain liquid crystalline elastomers containing the rigid mesogenic crosslinking agent M-1 and nematic monomer M-2 by a one-step hydrosilylation reaction is described. The chemical structures of the monomers and network polymers obtained were confirmed by FTIR and ¹H NMR spectroscopy. The mesomorphic properties and phase behaviour were investigated by differential scanning calorimetry, polarizing optical microscopy, and X-ray diffraction. The influence of the crosslinking units on phase behaviour is discussed. Liquid crystalline elastomers containing less than 15 mol % of the crosslinking units showed elasticity, reversible phase transitions and a threaded texture. The experimental results demonstrated that the glass transition temperature of polymers P-1-7 increased with increasing concentration of crosslinking agent M-1; but the isotropic temperature and liquid crystalline range decreased slightly.     

Morphology,structure, and properties of in situ compatibilized linear low‐density polyethylene/polystyrene and linear low‐density polyethylene/high‐impact polystyrene blends

Blends of linear low‐density polyethylene (LLDPE) with polystyrene (PS) and blends of LLDPE with high‐impact polystyrene (HIPS) were prepared through a reactive extrusion method. For increased compatibility of the two blending components, a Lewis acid catalyst, aluminum chloride (AlCl₃), was adopted to initiate the Friedel–Crafts alkylation reaction between the blending components. Spectra data from Raman spectra of the LLDPE/PS/AlCl₃ blends extracted with tetrahydrofuran verified that LLDPE segments were grafted to the para position of the benzene rings of PS, and this confirmed the graft structure of the Friedel–Crafts reaction between the polyolefin and PS. Because the in situ generated LLDPE‐g‐PS and LLDPE‐g‐HIPS copolymers acted as compatibilizers in the relative blending systems, the mechanical properties of the LLDPE/PS and LLDPE/HIPS blending systems were greatly improved. For example, after compatibilization, the Izod impact strength of an LLDPE/PS blend (80/20 w/w) was increased from 88.5 to 401.6 J/m, and its elongation at break increased from 370 to 790%. For an LLDPE/HIPS (60/40 w/w) blend, its Charpy impact strength was increased from 284.2 to 495.8 kJ/m². Scanning electron microscopy micrographs showed that the size of the domains decreased from 4–5 to less than 1 μm, depending on the content of added AlCl₃. The crystallization behavior of the LLDPE/PS blend was investigated with differential scanning calorimetry. Fractionated crystallization phenomena were noticed because of the reduction in the size of the LLDPE droplets. The melt‐flow rate of the blending system depended on the competition of the grafting reaction of LLDPE with PS and the degradation of the blending components. The degradation of PS only happened during the alkylation reaction between LLDPE and PS. Gel permeation chromatography showed that the alkylation reaction increased the molecular weight of the blend polymer. The low molecular weight part disappeared with reactive blending. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 1837–1849, 2003     

Crystallographic report: Crystal structure of a two‐dimensional coordination polymer: tetraaqua‐1,2,4,5‐benzenetetracarboxylato(pyrazine)dizinc(II) dihydrate

The structure of {[Zn₂(1,2,4,5‐btc)(pz)(H₂O)₄]·2(H₂O)}_n (1,2,4,5‐btc = 1, 2, 4, 5‐benzenetetracarboxylate, pz = pyrazine) is a two‐dimensional coordination network. The zinc(II) center is in a distorted octahedral NO₅ coordination environment that is defined by one nitrogen atom of pyrazine, three oxygen atoms of carboxyl groups from 1,2,4,5‐benzenetetracarboxylate tetraanions and two water molecules. Copyright © 2003 John Wiley & Sons, Ltd.     

Poisson半群的边界值

在空间Ｌｐ（Ｒｎ），１≤ｐ＜∞中，Ｐｏｉｓｏｎ算子半群ｅ－－△ｚ是右半平面Ｒｅｚ＞０上的解析半群．本文考虑它的边界值，证明了闭稠定算子－ｉ－△对某个α≥０生成了一个指数有界（Ｉ＋－△）－α 半群．     

Crystallographic report: Crystal structure of a homoleptic lanthanide guanidinate complex: [Ph2NC(NCy)2]3Yb·2PhCH3

The title complex, [Ph₂NC(NCy)₂]₃Yb·2PhCH₃ is a monomer with a six‐coordinate ytterbium center ligated by six nitrogen atoms of three chelating bidentate guanidinate ligands. The coordination geometry around the lanthanide ion is best described as a distorted trigonal prism. Copyright © 2005 John Wiley & Sons, Ltd.     

PERIODIC SOLUTION TO PREDATOR-PREY CHAIN SYSTEM WITH IMPULSIVE EFFECTS AND BEDDINGTON-DEANGELIS FUNCTIONAL RESPONSE

In this paper, a predator-prey chain system with impulsive effects and Beddington-DeAngelis functional response is studied. We investigate the existence of periodic solu-tion by coincidence degree theory. Sufficient conditions are obtained for the existence of periodic solution.