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841.
842.
基于10级模块串联的1 MV快脉冲直线型变压器驱动源装置,分别开展了1~3个模块在不充电或不触发时装置的整体输出参数测试。结果表明,在二极管负载阻抗基本不变的情况下,装置输出电流和电压降低的数值约为故障模块数与总模块数的比值。与所有模块正常工作时相比,脉冲上升时间分别增加10,22和32 ns,脉冲宽度分别增加13,23和48 ns。根据电路分析以及模块实际电参数建立了装置的等效电路模型,模拟得到的不同数量模块不工作时的输出电压变化趋势与实验结果基本一致,并利用电路模型对故障模块中开关两端的电压进行了模拟和分析。 相似文献
843.
[reaction: see text] Reductive alkylation of 5-methoxy-1-tetralone (6) with 2,3-dibromopropene gave an equilibrium mixture of bicyclic diones 7 (51%) and 8 (35%). Radical cyclization of 7 afforded tricyclic dione 5 (84%), which was reduced, cyclized, and dehydrated to give tetracyclic alkene 13 in 63% yield. Allylic oxidation of 13 with SeO2 and activated MnO2 afforded enone 2 in 85% yield, thereby completing a short formal synthesis of (+/-)-platensimycin. 相似文献
844.
Goulay F Osborn DL Taatjes CA Zou P Meloni G Leone SR 《Physical chemistry chemical physics : PCCP》2007,9(31):4291-4300
The reactions of the ethynyl radical (C(2)H) with propyne and allene are studied at room temperature using an apparatus that combines the tunability of the vacuum ultraviolet radiation of the Advanced Light Source at Lawrence Berkeley National Laboratory with time-resolved mass spectrometry. The C(2)H radical is prepared by 193-nm photolysis of CF(3)CCH and the mass spectrum of the reacting mixture is monitored in time using synchrotron-photoionization with a dual-sector mass spectrometer. Analysis using photoionization efficiency curves allows the isomer-specific detection of individual polyynes of chemical formula C(5)H(4) produced by both reactions. The product branching ratios are estimated for each isomer. The reaction of propyne with ethynyl gives 50-70% diacetylene (H-C[triple bond]C-C[triple bond]C-H) and 50-30% C(5)H(4), with a C(5)H(4)-isomer distribution of 15-20% ethynylallene (CH(2)=C=CH-C[triple bond]CH) and 85-80% methyldiacetylene (CH(3)-C[triple bond]C-C[triple bond]CH). The reaction of allene with ethynyl gives 35-45% ethynylallene, 20-25% methyldiacetylene and 45-30% 1,4-pentadiyne (HC[triple bond]C-CH(2)-C[triple bond]CH). Diacetylene is most likely not produced by this reaction; an upper limit of 30% on the branching fraction to diacetylene can be derived from the present experiment. The mechanisms of polyynes formation by these reactions as well as the implications for Titan's atmospheric chemistry are discussed. 相似文献
845.
The synthesis of a new class of template-assembled oligomannose clusters as the mimics of the epitope of the HIV-neutralizing antibody 2G12 is described. The novel oligomannose clusters were successfully assembled on a cyclic decapeptide template using the Cu(I)-catalyzed 1,3-dipolar cycloaddition of azides to alkynes by introducing four units of a synthetic D1 arm tetrasaccharide (Manalpha1,2Manalpha1,2Manalpha1,3Manalpha-) of high-mannose N-glycan on one face of the template and two T-helper epitope peptides on the other face of the template. Their binding to human antibody 2G12 was studied using surface plasmon resonance (SPR) technology. It was found that while the synthetic monomeric D1 arm oligosaccharide and its fluorinated derivative interacted with 2G12 only weakly, the corresponding template-assembled oligosaccharide clusters showed high affinity to antibody 2G12, indicating a clear clustering effect in 2G12 recognition. Interestingly, the fluorinated D1 arm cluster, in which the 6-OH of the terminal mannosyl residue was replaced with a fluorine atom, showed a distinct kinetic model in 2G12 binding as compared with the cluster of the natural D1 arm oligosaccharides. The oligosaccharide clusters with varied length of spacer demonstrated different affinity to 2G12, suggesting that an appropriate spatial orientation of the sugar chains in the cluster was crucial for high affinity binding to the antibody 2G12. It was also found that the introduction of two T-helper epitopes onto the template did not affect the structural integrity of the oligomannose cluster. The novel synthetic glycoconjugates represent a new type of immunogen that may be able to raise carbohydrate-specific neutralizing antibodies against HIV-1. 相似文献
846.
The interactions of nonionic meso-tetra(p-hydroxyphenyl)porphyrin (THPP) with CX3COOH (X = F, Cl, Br) in Triton X-100 (TX) micellar solution have been investigated by optical absorption, resonance light-scattering, and fluorescence spectroscopies. The double red-shifted absorption bands and strong resonance light scattering (RLS) signal imply that the assemblies induced by trihalo acetic acids belong to J-aggregates. The fluorescence of porphyrin is quenched due to the aggregate formation. The kinetics of assemblies trigged by CBr3COOH is studied via stopped-flow techniques. No characteristics of autocatalyzed reactions are observed, and there is only a log phase. The nature of the exciton coupling of transition dipole moment can be systematically changed by the haloid substituents of the organic counteranion. 相似文献
847.
848.
Yao X Wu C Du A Zou J Zhu Z Wang P Cheng H Smith S Lu G 《Journal of the American Chemical Society》2007,129(50):15650-15654
Synergistic effect of metallic couple and carbon nanotubes on Mg results in an ultrafast kinetics of hydrogenation that overcome a critical barrier of practical use of Mg as hydrogen storage materials. The ultrafast kinetics is attributed to the metal-H atomic interaction at the Mg surface and in the bulk (energy for bonding and releasing) and atomic hydrogen diffusion along the grain boundaries (aggregation of carbon nanotubes) and inside the grains. Hence, a hydrogenation mechanism is presented. 相似文献
849.
Short oxidized multi-walled carbon nanotubes (CNT) were derivatized with fluorescein isothiocyanate (FITC). Capillary electrophoresis
coupled with laser-induced fluorescence (CE–LIF) was then used to separate and detect the fluorescently labeled carbon-nanotube
probes (CNTP) in multidrug-resistant cells (K562A) and the parent cells (K562S). Greater expression of P-glycoprotein in K562A
cells than in K562S cells was confirmed by use of anti-P-glycoprotein antibody and flow-cytometric analysis. Analyses of CNTP
in both cell lines using both CE–LIF and flow cytometry showed that CNTP could traverse the cellular membrane without being
pumped out by P-glycoprotein. The CNTP distributed in both cell lines was analyzed at the single cell level and the results
were compared with those from analysis of ten cells and of the lysate from bulk cells. The results revealed the CE–LIF method
could be used for quantitative analysis of CNT in single cells in studies of drug delivery and multidrug resistance.
相似文献
850.