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61.
Leon O. Chua Chwen-Cher Chang 《International Journal of Circuit Theory and Applications》1987,15(2):143-170
A new simple circuit model for the MOS (metal-oxide-semiconductor) structure is presented. the model consists of three elements, namely, a linear capacitor, a non-linear capacitor and a C-dynamic element. Each component bears a simple relationship to the physical operating mechanism inside the MOS structure. the model can be used for simulating arbitrary MOS structure circuits under all operating conditions. In particular, it is capable of reproducing the structure's frequency-dependent small-signal characteristics. the model is also shown to exhibit many important and interesting dynamic behaviours under forward, reverse and sinusoidal operating modes. The model is based mainly upon the device's physical operating principles. But perhaps the most significant implication of this model is that it is the first ever to use a dynamic element to model the MOS structure from a physical approach. 相似文献
62.
Mechanical activation before carbothermic reduction can substantially enhance the formation of SiC from SiO2 and carbon mixtures. However, the morphology (e.g., particles or whiskers) of SiC formed from mechanically activated SiO2 and carbon mixtures is dependent of the degree of mechanical activation and the condition of the subsequent carbothermic reduction. These phenomena are investigated and rationalized based on the increased reactivity of the reactants and SiC formation mechanisms. 相似文献
63.
Kun-San Chen T. Leon Yu Yung-Sin Chen Tsang-Lang Lin Wen-Jiun Liu 《Journal of Polymer Research》2001,8(2):99-109
Polyester based polyurethanes were synthesized from 4,4′-methylene bis(phenyl isocyanate) (MDI) with butanediol as a chain
extender and low molecular weight polyester-diol as a soft segment. Three polyesters were used in the synthesis of polyurethanes.
Two of the polyesters, with molecular weight Mn = 2,660 and 2,155, were synthesized from adipic acid and 1,6-hexanediol, which had an even number of carbon atoms (polyester-6-6-1
and polyester-6-6-2). The other polyester with Mn = 2,770 was synthesized from pimelic acid and 1,5-pentanediol, which had an odd number of carbon atoms (polyester-7-5). Polyester-6-6-1
and polyester-6-6-2 consisting of even carbon monomers, had a higher degree of crystallinity at room temperature than polyester-7-5,
which consists of an odd number of carbon monomers. The effect of polyester molecular weight and soft and hard-segmental geometric
structure on the soft-and hard-segmental phase segregation was studied using differential scanning calorimetry (DSC), Fourier
transform infrared spectroscopy (FTIR), and small angle X-ray scattering (SAXS). 相似文献
64.
Fuchs Stefan Leveles Laszlo Seshan K. Lefferts Leon Lemonidou Angeliki Lercher Johannes A. 《Topics in Catalysis》2001,15(2-4):169-174
The oxidative dehydrogenation and cracking of ethane and propane over LiDyMg mixed oxides is reported. High yields of olefins and only moderate formation of carbon oxides was observed. Both are primary products that hardly interconvert under the reaction conditions used. Addition of chloride increases the rate of reaction, while slightly decreasing the selectivity to olefins. The addition of carbon dioxide strongly decreases the rate of reaction, the negative order of 0.5 indicating that two active Li+sites are blocked by the adsorption of one CO2molecule. The reaction proceeds at low oxygen pressure primarily via elimination of dihydrogen, while at higher oxygen partial pressure the hydrogen elimination occurs via water formation. It is speculated that dehydrogenation and cracking involve Li+and a rather nucleophilic oxygen site. 相似文献
65.
Leon Wehrhan Prof. Dr. Alexander Hillisch Dr. Stefan Mundt Dr. Adrian Tersteegen Dr. Katharina Meier 《ChemMedChem》2020,15(21):2010-2018
Target druggability assessment is an integral part of the early target characterization and selection process in pharmaceutical industry. Here, we investigate a set of five different serine proteases from the blood coagulation cascade. The aim of this study is twofold. Firstly, leveraging the wealth of available in-house high-throughput screening (HTS) data, we analyze HTS hit rates and discuss their predictive value for the development of small molecule (SMOL) candidates. Purely structure-activity relationship (SAR) based druggability ratings are compared with computational protein-structure based druggability assessments. Secondly, we evaluate the impact of using conformational ensembles from molecular dynamics (MD) simulations instead of single static crystal structures as basis for computational druggability assessments. Based on this study, we recommend incorporating molecular dynamics routinely into the early target characterization process, especially if only a single X-ray structure is available. 相似文献
66.
Wilco MH Verbeeten Marc JW Kanters Tom AP Engels Leon E Govaert 《Polymer International》2015,64(11):1527-1536
A methodology for structural analysis simulations is presented that incorporates the distribution of mechanical properties along the geometrical dimensions of injection‐moulded amorphous polymer products. It is based on a previously developed modelling approach, where the thermomechanical history experienced during processing was used to determine the yield stress at the end of an injection‐moulding cycle. Comparison between experimental data and simulation results showed an excellent quantitative agreement, both for short‐term tensile tests as well as long‐term creep experiments over a range of strain rates, applied stresses, and testing temperatures. Changes in mould temperature and component wall thickness, which directly affect the cooling profiles and, hence, the mechanical properties, were well captured by the methodology presented. Furthermore, it turns out that the distribution of the yield stress along a tensile bar is one of the triggers for the onset of the (strong) localization generally observed in experiments. © 2015 Society of Chemical Industry 相似文献
67.
Rei‐Mei Chou Chi‐Chin Chang T Leon Yu Yu‐Hsien Tseng Mo‐Jyi Wu 《Polymer International》2001,50(2):213-221
The crystallization kinetics of poly(butylene terephthalate) (PBT), poly(ethylene terephthalate) (PET), and their copolymers poly(1,4‐butylene‐co‐ethylene terephthalate) (PBET) containing 70/30, 65/35 and 60/40 molar ratios of 1,4‐butanediol/ethylene glycol were investigated using differential scanning calorimetry (DSC) at crystallization temperatures (Tc) which were 35–90 °C below equilibrium melting temperature . Although these copolymers contain both monomers in high proportion, DSC data revealed for copolymer crystallization behaviour. The reason for such copolymers being able to crystallize could be due to the similar chemical structures of 1,4‐butanediol and ethylene glycol. DSC results for isothermal crystallization revealed that random copolymers had a lower degree of crystallinity and lower crystallite growth rate than those of homopolymers. DSC heating scans, after completion of isothermal crystallization, showed triple melting endotherms for all these polyesters, similar to those of other polymers as reported in the literature. The crystallization isotherms followed the Avrami equation with an exponent n of 2–2.5 for PET and 2.5–3.0 for PBT and PBETs. Analyses of the Lauritzen–Hoffman equation for DSC isothermal crystallization data revealed that PBT and PET had higher growth rate constant Go, and nucleation constant Kg than those of PBET copolymers. © 2001 Society of Chemical Industry 相似文献
68.
Phylogenetic Studies,Gene Cluster Analysis,and Enzymatic Reaction Support Anthrahydroquinone Reduction as the Physiological Function of Fungal 17β‐Hydroxysteroid Dehydrogenase 下载免费PDF全文
Leon Fürtges David Conradt Dr. Michael A. Schätzle Shailesh Kumar Singh Dr. Nada Kraševec Prof. Dr. Tea Lanišnik Rižner Prof. Dr. Michael Müller Dr. Syed Masood Husain 《Chembiochem : a European journal of chemical biology》2017,18(1):77-80
17β‐Hydroxysteroid dehydrogenase (17β‐HSDcl) from the filamentous fungus Curvularia lunata (teleomorph Cochliobolus lunatus) catalyzes NADP(H)‐dependent oxidoreductions of androgens and estrogens. Despite detailed biochemical and structural characterization of 17β‐HSDcl, its physiological function remains unknown. On the basis of amino acid sequence alignment, phylogenetic studies, and the recent identification of the physiological substrates of the homologous MdpC from Aspergillus nidulans and AflM from Aspergillus parasiticus, we propose an anthrahydroquinone as the physiological substrate of 17β‐HSDcl. This is also supported by our analysis of a secondary metabolite biosynthetic gene cluster in C. lunata m118, containing 17β‐HSDcl and ten other genes, including a polyketide synthase probably involved in emodin formation. Chemoenzymatic reduction of emodin by 17β‐HSDcl in the presence of sodium dithionite verified this hypothesis. On the basis of these results, the involvement of a 17β‐HSDcl in the biosynthesis of other anthrahydroquinone‐derived natural products is proposed; hence, 17β‐HSDcl should be more appropriately referred to as a polyhydroxyanthracene reductase (PHAR). 相似文献
69.
Manganese(II) acetate reacts with phthalic acid (phH(2)) to give [Mn(ph)].0.5H(2)O (1). Reaction of 1 with 1,10-phenanthroline produces [Mn(ph)(phen)].2H(2)O (2) and [Mn(ph)(phen)(2)(H(2)O)].4H(2)O (3). Reaction of isophthalic acid (isophH(2)) with manganese(II) acetate results in the formation of [Mn(isoph)].2H(2)O (4). The addition of the N,N-donor ligands 1,10-phenanthroline or 2,2'-bipyridine to 4 leads to the formation of [Mn(2) (isoph)(2)(phen)(3))].4H(2)O (5), [(Mn(phen)(2)(H(2)O)(2)](2)(isoph)(2)(phen).12H(2)O (6) and {[Mn(isoph)(bipy)](4).2.75 biby}(n) (7), respectively. Molecular structures of 3, 6 and 7 were determined crystallographically. In 3 the phthalate ligand is bound to the manganese via just one of its carboxylate groups in a monodentate mode with the remaining coordination sites filled by four phenanthroline nitrogen and one water oxygen atoms. In 6 the isophthalates are uncoordinated with the octahedral manganese center ligated by two phenanthrolines and two waters. In 7 the Isophthalate ligands act as bridges resulting in a polymeric structure. One of the carboxylate groups is chelating a single manganese with the other binding two metal centres in a bridging bidentate mode. The phthalate and isophthalate complexes, the metal free ligands and a number of simple manganes salts were each tested for their ability, to inhibit the growth of Candida albicans. Only the "metal free" 1,10-phenanthroline and its manganese complexes were found to be active. 相似文献
70.
Tams Roska Leon O. Chua 《International Journal of Circuit Theory and Applications》1992,20(5):469-481
The cellular neural network (CNN) paradigm is a powerful framework for analogue non-linear processing arrays placed on a regular grid. In this paper we extend the current repertoire of CNN cloning template elements (atoms) by introducing additional non-linear and delay-type characteristics. In addition, architectures with non-uniform processors and neighbourhoods (grid sizes) are introduced. With this generalization, several well-known and powerful analogue array-computing structures can be interpreted as special cases of the CNN. Moreover, we show that the CNN with these generalized cloning templates has a general programmable circuit structure (a prototype machine) with analogue macros and algorithms. the relations with the cellular automaton (CA) and the systolic array (SA) are analysed. Finally, some robust stability results and the state space structure of the dynamics are presented. 相似文献