排序方式: 共有109条查询结果,搜索用时 15 毫秒
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The front dynamics driven by a convection field in a model of FitzHugh-Nagumo type is studied both analytieMly and numerically. Saddle-node bifurcation induced by the convection field is found by using a singular perturbation analysis of front solutions. Convection field accelerates the B1och front propagating opposite the direction of convection field, but inhibits the Bloch front propagating along the direction of convection field. In addition convection field drives Ising front to travel opposite the direction of convection field. 相似文献
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利用Cluster-cluster aggregation (CCA)模型,模拟了由相同数目球形原始微粒凝聚而成的四种随机取向气溶胶凝聚粒子.根据物质的电结构,将气溶胶凝聚粒子离散为一系列偶极子,结合离散偶极子近似方法,在获得每一个偶极子的电偶极矩之后,数值计算了气溶胶凝聚粒子散射强度的角分布,并分析了散射强度随入射光入射角度和气溶胶凝聚粒子尺寸参数变化的规律.结果显示:当散射角较小时,气溶胶凝聚粒子取向和入射光的入射角度对散射强度影响不大,当散射角增大时,散射强度则明显依赖于气溶胶凝聚粒子取向和入射光的入射角度;对于不同尺寸参数的气溶胶凝聚粒子,在同一角度入射情况下,随尺寸参数的增加,气溶胶凝聚粒子的散射主要集中于前向散射. 相似文献
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WEN Li-Rong QI Wen-Ying LIYa-Feng LI Ming SUN En-Tao 《结构化学》2007,26(7):811-816
The title compound (C22H22N2O2Fe·CH3OH) was synthesized via a one-pot proce- dure from ferrocenylaldehyde, malononitrile and 5,5-dimethyl-1,3-cyclohexanedione using room temperature ionic liquid and pyridine as the catalysts, and characterized by elemental analysis, IR and 1H NMR. The structure was determined by X-ray single-crystal diffraction. The crystal belongs to monoclinic system, space group P21/n, with a = 9.7085(15), b = 22.951(4), c = 9.987(2) A, β = 112.494(3)°, V = 2055.9(6) A3, Z = 4, Mr = 402.28, Dc = 1.403 g/cm3, μ = 0.759 mm-1, F(000) = 868, the final R = 0.0536 and wR = 0.1449 for 4202 observed reflections with I > 2σ(I). The supramolecular single-helix chain of the title compound is formed by linking the building units with the hydrogen bond between N1 and N2. The adjacent chains are connected to a 2D layer by the hydrogen bond between N1 and O1. The adjacent layers are further linked by van der waals’ force. The CH3OH molecule is trapped in the interlayer. 相似文献
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Yang W Zhou YF Dai HP Bi LJ Zhang ZP Zhang XH Leng Y Zhang XE 《Analytical and bioanalytical chemistry》2008,390(8):2133-2140
Methyl parathion hydrolase (MPH) is an enzyme that catalyzes the degradation of methyl parathion, generating a yellow product
with specific absorption at 405 nm. The application of MPH as a new labeling enzyme was illustrated in this study. The key
advantages of using MPH as a labeling enzyme are as follows: (1) unlike alkaline phosphatase (AP), horseradish peroxidase
(HRP), and glucose oxidase (GOD), MPH is rarely found in animal cells, and it therefore produces less background noise; (2)
its active form in solution is the monomer, with a molecular weight of 37 kDa; (3) its turnover number is 114.70 ± 13.19 s−1, which is sufficiently high to yield a significant signal for sensitive detection; and (4) its 3D structure is known and
its C-terminal that is exposed to the surface can be easily subjected to the construction of genetic engineering monocloning
antibody–enzyme fusion for enzyme-linked immunosorbent assay (ELISA). To demonstrate its utility, MPH was ligated to an single-chain
variable fragment (scFv), known as A1E, against a white spot syndrome virus (WSSV) with the insertion of a [–(Gly–Ser)5–] linker peptide. The resulting fusion protein MPH-A1E possessed both the binding specificity of the scFv segment and the
catalytic activity of the MPH segment. When MPH-A1E was used as an ELISA reagent, 25 ng purified WSSV was detected; this was
similar to the detection sensitivity obtained using A1E scFv and the HRP/Anti-E Tag Conjugate protocol. The fusion protein
also recognized the WSSV in 1 μL hemolymph from an infected shrimp and differentiated it from a healthy shrimp.
Figure The 3-D structure of MPH. (a) monomer showing C- and N-terminals; (b) the crystal structure of the dimer
W. Yang and Y.-F. Zhou contributed equally to this work. 相似文献
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Li-Ya Niu Hui Li Liang Feng Ying-Shi Guan Yu-Zhe Chen Chun-Feng Duan Li-Zhu Wu Ya-Feng Guan Chen-Ho Tung Qing-Zheng Yang 《Analytica chimica acta》2013
A BODIPY(4,4-difluoro-4-bora-3a,4a-diaza-s-indacene)-based fluorometric sensor array has been developed for the highly sensitive detection of eight heavy-metal ions at micromolar concentration. The di-2-picolyamine (DPA) derivatives combine high affinities for a variety of heavy-metal ions with the capacity to perturb the fluorescence properties of BODIPY, making them perfectly suitable for the design of fluorometric sensor arrays for heavy-metal ions. 12 cross-reactive BODIPY fluorescent indicators provide facile identification of the heavy-metal ions using a standard chemometric approach (hierarchical clustering analysis); no misclassifications were found over 45 trials. Clear differentiation among heavy-metal ions as a function of concentration was also achieved, even down to 10−7 M. A semi-quantitative interpolation of the heavy-metal concentration is obtained by comparing the total Euclidean distance of the measurement with a set of known concentrations in the library. 相似文献
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传统的微孔晶体材料是以硅酸盐、硅铝酸盐、磷铝酸盐和无机金属磷酸盐等作为结构的骨架[1,2]. 近几年来, 出现了一类新型的无机-有机杂化微孔晶体材料, 这类晶体材料是用刚性和热稳定性较好的有机分子(如芳香多酸和多碱)和金属离子作为骨架的结构单元. 它们能够在去除孔道中的溶剂分子后仍然保持骨架的完整性, 而且其孔道的直径在0.4~1.0 nm之间, 比表面积远大于相似孔道的分子筛. 因此, 这类材料具有许多潜在的特殊性能, 在选择性催化、分子识别和可逆性主客体分子(离子)交换等方面具有诱人的应用前景. Yaghi等[3~11]利用不同的有机分子和各种金属制备出了许多这类晶体材料. 对苯二酸是常见的有机配体, 以它和金属离子为结构骨架所形成的无机-有机杂化微孔晶体有Zn3(BDC)3*(CH3OH),Zn(BDC)*(DMF)(H2O),(TPT)(Py)Cd和Zn4O(BDC)3*(DMF)8(C6H5Cl)等[12~15], 但在对苯二酸与金属构成的骨架中, 由于有多个乙二醇分子配位, 很少形成稳定的三维骨架结构的无机-有机杂化微孔晶体. 相似文献