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Antonio Lor?´a 《Chaos, solitons, and fractals》2011,44(9):702-709
We discuss the cascaded-based controlled synchronization method for hyperchaotic systems. The control approach is based on analysis tools for cascaded time-varying systems. That is, the closed-loop system takes the form of two subsystems which are interconnected in a manner that the state of one system enters into another but without feedback loop. The advantage of such construction is that the controller is largely simplified relative to other design methods such as backstepping. We apply the method to Chen’s hyperchaotic system and show that global synchronization is achieved via linear control. Also, we assume that only three instead of four control inputs are available. The method is tested in numerical simulations. 相似文献
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Clusters of galaxies are excellent probes of cosmic structure and evolution. X-ray studies of clusters provide some of their
key parameters, viz., temperature of the hot intra-cluster gas, its metallicity, X-ray luminosity and surface brightness giving
mass distribution and mass-flow rate in the case of cooling flows. X-ray measurements for a large sample of clusters have
lead to estimates of the total gravitating mass in them, which can be compared to the virial masses derived from dynamical
considerations and gravitational lensing in some of them. X-ray derived total masses are consistent with masses obtained from
the other methods after the effects due to the presence of cooling flows are taken into account in the analyses. Estimated
virial masses, lack of evolution in X-ray properties, and detection of several very hot clusters at high redshifts indicate
a Universe with a low value (≤ 0.3) for the Ω parameter. 相似文献
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Vlaar MJ Lor MH Ehlers AW Schakel M Lutz M Spek AL Lammertsma K 《The Journal of organic chemistry》2002,67(8):2485-2493
Six novel dispirophosphirane complexes have been synthesized from the reaction of bicycloalkylidenes with the electrophilic phosphinidene complex PhPW(CO)(5). They contain a central phosphirane ring, which is spirofused on one side to a cyclopropane or cyclobutane ring and on the other side with a three-, four-, five-, or six-membered ring. Their crystal structures and MP2/6-31G-computed geometries for simplified parent systems suggest that spirofusion with small rings results in a tightening of the central three-membered phosphaheterocycle, while spirofusion with larger rings results in a relaxation of the phosphirane geometry. Similar theoretical predictions are made for the corresponding annulated hydrocarbons. Strain energies for both the hydrocarbon and phosphorus series of structures have been calculated at G3(MP2). Whereas the [3]triangulane hydrocarbon and phospha[3]triangulane have a significant excess strain of 8.1 and 5.2 kcal/mol per spiroatom, respectively, the excess strain for systems spirofused with larger rings are negligible for the hydrocarbons and even negative for the phosphorus-containing species because of hyperconjugative stabilization. 相似文献
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Churchard AJ Banach E Borgschulte A Caputo R Chen JC Clary D Fijalkowski KJ Geerlings H Genova RV Grochala W Jaroń T Juanes-Marcos JC Kasemo B Kroes GJ Ljubić I Naujoks N Nørskov JK Olsen RA Pendolino F Remhof A Románszki L Tekin A Vegge T Zäch M Züttel A 《Physical chemistry chemical physics : PCCP》2011,13(38):16955-16972
The widespread adoption of hydrogen as an energy carrier could bring significant benefits, but only if a number of currently intractable problems can be overcome. Not the least of these is the problem of storage, particularly when aimed at use onboard light-vehicles. The aim of this overview is to look in depth at a number of areas linked by the recently concluded HYDROGEN research network, representing an intentionally multi-faceted selection with the goal of advancing the field on a number of fronts simultaneously. For the general reader we provide a concise outline of the main approaches to storing hydrogen before moving on to detailed reviews of recent research in the solid chemical storage of hydrogen, and so provide an entry point for the interested reader on these diverse topics. The subjects covered include: the mechanisms of Ti catalysis in alanates; the kinetics of the borohydrides and the resulting limitations; novel transition metal catalysts for use with complex hydrides; less common borohydrides; protic-hydridic stores; metal ammines and novel approaches to nano-confined metal hydrides. 相似文献
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Callebaut G Mangelinckx S Kiss L Sillanpää R Fülöp F De Kimpe N 《Organic & biomolecular chemistry》2012,10(11):2326-2338
The efficient asymmetric synthesis of new chiral γ-chloro-α,β-diamino acid derivatives via highly diastereoselective Mannich-type reactions of N-(diphenylmethylene) glycine esters across a chiral α-chloro-N-p-toluenesulfinylimine was developed. The influence of the base, LDA or LiHMDS, used for the formation of the glycine enolates, was of great importance for the anti-/syn-diastereoselectivity of the Mannich-type reaction. The γ-chloro-α,β-diamino acid derivatives proved to be excellent building blocks for ring closure towards optically pure anti- and syn-β,γ-aziridino-α-amino esters, and subsequent ring transformation into trans-3-aminoazetidine-2-carboxylic acid derivatives and α,β-diamino-γ-butyrolactones. 相似文献
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Anas Semghouli Dr. Zsanett Benke Dr. Attila M. Remete Tamás T. Novák Prof. Santos Fustero Prof. Loránd Kiss 《化学:亚洲杂志》2021,16(23):3873-3881
Novel functionalized azaheterocycles with multiple chiral centers have been accessed from readily available norbornene β-amino acids or β-lactams across a stereocontrolled synthetic route, based on ring-opening metathesis (ROM) of the staring unsaturated bicyclic amino esters, followed by selective cyclization through ring-closing metathesis (RCM). The RCM transformations have been studied under various experimental conditions to assess the scope of conversion, catalyst, yield, and substrate influence. The structure of the starting norbornene β-amino acids predetermined the structure of the new azaheterocycles, and the developed synthetic route took place with the conservation of the configuration of the chiral centers. 相似文献
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Maria Pihl Krzysztof Kolman Antiope Lotsari Marie Ivarsson Erich Schüster Niklas Lorén 《Journal of Dispersion Science and Technology》2019,40(4):555-562
Development of multi-purpose probes for mass transport measurements is of importance to gain knowledge in diffusional behaviour in heterogeneous structures such as food, hygiene or pharamceuticals. By combining different techniques, such as Fluorescence Recovery After Photobleaching (FRAP) and Nuclear Magnetic Resonance Diffusometry (NMR-d), information of both local and global diffusion can be collected and used to gain insights on for example material heterogeneities and probe-material interactions. To obtain a FRAP-responsive probe, fluorescent silica particles were produced using fluorescent preconjugates added in a modified Stöber process. A NMR-d responsive moiety was introduced by derivatizing the fluorescent silica particles with polyethylene glycol. The particle size distributions were determined by dynamic light scattering and transmission electron microscopy and these measurements were compared to value extrapolated from diffusion measurements using FRAP and NMR-d. The good agreement between the FRAP and NMR-d measurements demonstrates the potential of multi-purpose probes for future applications concerning mass transport at local and global scale simultaneously. 相似文献
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