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891.
892.
Ren X Xue Y Liu J Zhang K Zheng J Luo G Guo C Mu Y Shen J 《Chembiochem : a European journal of chemical biology》2002,3(4):356-363
A novel dicyclodextrinyl ditelluride (2-TeCD) compound was devised as a functional mimic of the glutathione peroxidase (GPX) enzymes that normally remove hydroperoxides from the cell. The GPX activity of the mimic was found to be 46.7 U microM(-1), which is 46 times as active as Ebselen, a well-known GPX mimic. A detailed steady-state kinetic study was undertaken to probe the reason for the high catalytic efficiency of 2-TeCD. This high efficiency can be explained based on both the binding of the substrate to the cyclodextrin and the catalytic mechanism of 2-TeCD, which is different from that of diselenide compounds. 2-TeCD exhibits good water solubility and is chemically and biologically stable. The biological effect of 2-TeCD was evaluated by its ability to protect mitochondria from oxidative damage. 2-TeCD exhibited excellent antioxidant capacity in comparison with Ebselen. 相似文献
893.
894.
895.
纤维素LiCl/DMAc体系的溶液特征 总被引:4,自引:0,他引:4
本文研究了纤维素LiCl/DMAc体系的溶液特征。实验结果证明该体系具有良好的时间稳定性和热稳定性,能在常温下近30天内没有明显的粘度降低;在100℃高温下,4h不降解。同时测定了溶液的特性粘数和Huggins常数,Huggins常数在0.4~0.6之间,对比纤维素的铜乙二胺(Cuen)溶液,发现特性粘数[η]LICI/DMAc>[η]Cuen,无扰尺寸ALiCi/DMAc>ACuen,可见在LiCl/DMAc体系中,溶剂与纤维素分子表现出更强的相互作用力,分子链充分伸展。该体系的特性粘数、粘度常数不仅与温度、溶剂有关,而且是LiCl浓度的函数,具有与聚电解质溶液相类似的性质。这可能是因为纤维素分子链上的H质子和溶液中的Cl-离子相互作用,而使纤维素分子带上部分电荷,相互排斥而引起的。因此利用M-H方程测分子量,粘度常数的确立必须考虑诸多因素的影响,否则会导致分子量的高估。 相似文献
896.
Flaky monoclinic La2Ti2O7 was prepared via a hydrothermal method based on the reaction of Ti(SO4)2 and La(NO3)3. Relative to the solid-state reaction sample, the flaky La2Ti2O7 showed higher surface areas, much smaller crystal size and more efficient light absorption. All these factors led to the
higher photoactivity to produce H2 from water splitting under UV irradiation. 相似文献
897.
898.
A novel sol–gel method based on V2O5·nH2O hydro-gel was developed to synthesize nanocrystalline Li3V2(PO4)3/carbon composite material. In this route, V2O5·nH2O hydro-gel, NH4H2PO4, Li2CO3 and high-surface-area carbon were used as starting materials to prepare precursor, and the Li3V2(PO4)3/carbon was obtained by sintering precursor at 750 °C for 4 h in flowing argon. The sol–gel synthesis ensures homogeneity of the precursors and improved reactivity. The sample was characterized by XRD, SEM and TEM. X-ray diffraction results show Li3V2(PO4)3 sample is monoclinic structure with the space group of P21/n. The TEM image indicates that the Li3V2(PO4)3 particles modified by conductive carbon are about 70 nm in diameter. The Li3V2(PO4)3/carbon system showed that the discharge capacities in the first and 50th cycle are about 155.3 and 143.6 mAh/g, respectively, in the range of 3.0–4.8 V. The sol–gel method is fit for the preparation of Li3V2(PO4)3/carbon composite material which may offer some favorable properties for commercial application. 相似文献
899.
Yun Huang Hai-Liang Zhang Dun-Shen Zhu Shou-Ke Yan Xiao-Fang Chen Er-Qiang Chen Qi-Feng Zhou 《Polymer》2006,47(4):1217-1225
Crystallization and melting of a poly(ethylene oxide) (PEO) diblock copolymer containing a tablet-like block of poly{2,5-bis[(4-methoxyphenyl)oxycarbonyl]styrene} (PMPCS) in ultrathin films have been studied using atomic force microscopy (AFM) coupled with a hot stage. The PEO and PMPCS block possess the number-average molecular weights (Mn) of 5300 and 2100 g/mol, respectively. The ultrathin films on the mica and glow-discharged carbon surfaces were obtained by static dilute solution casting at room temperature. Isothermal melt crystallization from ultrathin films always leads to flat-on lamellae. Selective area electron diffraction (SAED) experiments have demonstrated that the PEO blocks crystallize with a monoclinic structure identical to that of homo-PEO and the chain direction is perpendicular to the substrate. At Tc<44 °C, the monolayer crystals are dendrites. At Tc>48 °C, square-shaped crystals are formed with the (100) and (020) planes as the crystal edges. At 44 °C≤Tc≤48 °C, an intermediate monolayer morphology is observed. The monolayer thickness increases monotonically with increasing Tc. At the same Tc, the monolayer lamellae with the top and bottom amorphous layers contacting with the atmosphere and the substrate possess a significantly larger overall thickness than the long period of the crystals in bulk. For the spiral terraces induced by screw dislocation, the thickness of each terrace is close to that of the monolayer formed at the same Tc, and their melting is mainly determined by the terrace thickness. 相似文献
900.