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1.
2.
We investigate two families of Lorenz-like three-dimensional nonlinear dynamical systems (i) the generalized Lorenz system and (ii) the Burke–Shaw system. Analytical investigation of the former system is possible under the assumption (I) which in fact concerns four different systems corresponding to = ±1, m = 0, 1. The fixed points and stability characteristics of the Lorenz system under the assumption (I) are also classified. Parametric and temporal (t → ∞) asymptotes are also studied in connection to the memory of both the systems. We calculate the Lyapunov exponents and Lyapunov dimension for the chaotic attractors in order to study the influence of the parameters of the Lorenz system on the attractors obtained not only when the assumption (I) is satisfied but also for other values of the parameters σ, r, b, ω and m. 相似文献
3.
Yu Yang Maya Belghazi Arnaud Lagadec David J. Miller Steven B. Hawthorne 《Journal of chromatography. A》1998,810(1-2):149-159
The intermolecular interactions between organic solutes and sorbent matrices under subcritical water conditions have been investigated at a pressure of 50 bar and temperatures ranging from 50 to 250°C. Both polar and nonpolar organics (chlorophenols, amines, n-alkanes, and polycyclic aromatic hydrocarbons) and five different sorbent matrices (glass beads, alumina, Florisil, silica-bonded C18, and polymeric XAD-4 resins) were used. From the same matrix, the polar solutes always eluted at lower temperatures, while the moderately polar and nonpolar solutes only eluted at higher temperatures. Similar to matrix effects previously observed using supercritical carbon dioxide, the sorbent type greatly influenced the elution efficiency under subcritical water conditions. Lower temperatures are sufficient to elute a particular solute from glass beads, alumina, and Florisil, but higher temperatures (less polar water) are needed to elute the same solute from silica-bonded C18. The highest temperatures were required to elute aromatic organics from XAD-4. These matrix effects demonstrate that, while low temperature water can break inert or dipole interactions between solutes and glass beads, alumina, and Florisil, higher temperature water is required to interrupt the van der Waals attractions between solutes and silica-bonded C18, and even higher temperatures needed to overcome the π-electron interactions between aromatic solutes and XAD-4. 相似文献
4.
Irina G. Gazaryan Maya Yu. Rubtsova Yuri L. Kapeliuch José Neptuno Rodriguez-Lopez L. Mark Lagrimini Roger N. F. Thorneley 《Photochemistry and photobiology》1998,67(1):106-110
The properties of a newly isolated anionic tobacco peroxidase from transgenic tobacco plants overexpressing the enzyme have been studied with respect to the chemiluminescent reaction of luminol oxidation. These were compared to the properties of horseradish peroxidase in the cooxidation of luminol and p -iodophenol, the enhanced chemiluminescence reaction. The pH, luminol and hydrogen peroxide concentrations were optimized for maximum sensitivity using the tobacco enzyme. The detection limit for the latter under the optimal conditions (2.5 m M luminol, 2 m M hydrogen peroxide, 100 m M Naborate buffer, pH 9.3) was about 0.1 p M , which is at least five times lower than that for horseradish peroxidase in enhanced chemiluminescence with p -iodophenol. The rate constants for the elementary steps of the enzyme-catalyzed reaction have been determined: k 1 = 4.9 × 106 M −1 s1 , k 2 = 7.3 × 106 M −1 s−1 , k 3 = 2.1 × 106 M −1 s−1 (pH 9.3). The similarity of these rate constants is unusual for plant peroxidases. The high catalytic activity of tobacco peroxidase in the luminescent reaction is explained by the high reactivity of its Compound II toward luminol and the high stability of the holoenzyme with respect to heme dissociation. This seems to be a unique property of this particular enzyme among other plant peroxidases. 相似文献
5.
Recently, we introduced a class of generalized hypergeometric functionsI
n:(b
q)/α:(a
p) (x, w) by using a difference operator Δ
x,w
, where
. In this paper an attempt has been made to obtain some bilateral generating relations associated withI
n
ga
(x, w). Each result is followed by its applications to the classical orthogonal polynomials. 相似文献
6.
Dusanka Ž. Obadović Anikó Vajda Maya Garić A. Bubnov Vera Hamplová M. Kašpar Katalin Fodor-Csorba 《Journal of Thermal Analysis and Calorimetry》2005,80(2):519-523
Summary Thermal properties of a homologous series of ferroelectric liquid crystals S-(-)-[4-(2-n-alkoxy-propionyloxy)]biphenyl-4'-[n-alkoxy-(3,5-dimethyl)]benzoate have been investigated by polarizing optical microscopy and differential scanning calorimetry.
The mesophases were identified and confirmed by X-ray too. Three binary mixtures were prepared from the individual homologues.
In one of the mixtures (Mix1), the ferroelectric SmC* phase has broadened and became enantiotropic. This mesophase remained
monotropic in the other two mixtures (Mix2, Mix3). The chiral nematic N* phase did not appear in Mix1, but remained monotropic
for the other two mixtures. Two molecular parameters, the layer spacing and the average intermolecular distance have been
calculated from the X-ray results for the homologues and their mixtures. An intercalated tail-to-tail packing of molecules
was found both in the single compounds and their mixtures resulting in the layer spacing about half of the molecular length
of the single compounds. 相似文献
7.
Busch KW Swamidoss IM Fakayode SO Busch MA 《Journal of the American Chemical Society》2003,125(7):1690-1691
Multivariate statistical techniques were applied to the UV spectra of a series of solutions at pH 12 containing a fixed concentration (30 mM) of beta-cyclodextrin (beta-CD) and a fixed concentration (15 mM) of 2-phenylglycine (phi-Gly) with various known enantiomeric compositions. Multivariate correlation of the spectral data for the solutions containing the phi-Gly/beta-CD guest-host complexes with the known enantiomeric composition of the phi-Gly samples was accomplished by partial-least-squares regression. When the multivariate model was used to predict the enantiomeric purity of a test set of samples over the mol fraction range of 0.5-0.9 R-phi-Gly, the average magnitude of the relative errors in the mol fraction determination of enantiomeric composition was 3%. A plot of the enantiomeric composition predicted by the model versus the known enantiomeric composition of the calibration set gave a straight line with a correlation coefficient of 0.955, a slope of 1.05, and an offset of 5.61 x 10-4. 相似文献
8.
Miyagi K Sampson RW Sieber-Blum M Sieber F 《Journal of photochemistry and photobiology. B, Biology》2003,70(3):133-144
The purpose of this study was to determine in a preclinical purging model, how effective crystal violet-mediated photodynamic therapy (CV-PDT) is against solid tumor and drug-resistant mutant tumor cells, and if certain limitations of CV-PDT can be overcome by using crystal violet (CV) in combination with the membrane-active photosensitizer, Merocyanine 540 (MC540). When used under conditions that preserved an adequate fraction of normal human granulocyte/macrophage progenitors (CFU-GM), CV-PDT failed to achieve meaningful reductions of DU145 prostate, H69 small cell lung cancer, and MDA-MB-435S breast cancer cells. Melphalan-resistant L1210/L-PAM1, adriamycin-resistant P388/ADR, and adriamycin-resistant HL-60/ADR leukemia cells were markedly less sensitive to CV-PDT than their wild-type counterparts, whereas cisplatin-resistant H69/CDDP cells were more sensitive than wild-type H69 cells. Sequential exposure to MC540- and CV-PDT under conditions that preserved an adequate fraction (73% and 29%, respectively) of normal CD34-positive hematopoietic stem cells and granulocyte/macrophage progenitors was highly effective against H69 (99.997% reduction) and H69/CDDP (99.999% reduction) cells, but ineffective against HL-60/ADR, MDA-MB-435S, and DU145 cells. CV thus shows only limited promise as a single-modality purging agent. However, in certain situations, clinically meaningful tumor cell depletions can be obtained by using CV in combination with a second photosensitizer such as MC540. 相似文献
9.
Oleg A. Raitman Andrei B. Kharitonov Maya Zayats Eugenii Katz Itamar Willner 《Analytica chimica acta》2004,504(1):101-111
Crosslinked films consisting of the acrylamide-acrylamidophenylboronic acid copolymer that are imprinted with recognition sites for β-nicotinamide adenine dinucleotide (NAD+), β-nicotinamide adenine dinucleotide phosphate NADP+, and their reduced forms (NAD(P)H), are assembled on Au-coated glass supports. The binding of the oxidized cofactors NAD+ or NADP+ or the reduced cofactors NADH or NADPH to the respective imprinted sites results in the swelling of the polymer films through the uptake of water. Surface plasmon resonance (SPR) spectroscopy is employed to follow the binding of the different cofactors to the respective imprinted sites. The imprinted recognition sites reveal selectivity towards the association of the imprinted cofactors. The method enables the analysis of the NAD(P)+ and NAD(P)H cofactors in the concentration range of 1×10−6 to 1×10−3 M. The cofactor-imprinted films associated with the Au-coated glass supports act as active interfaces for the characterization of biocatalyzed transformations that involve the cofactor-dependent enzymes. This is exemplified with the characterization of the biocatalyzed oxidation of lactate to pyruvate in the presence of NAD+ and lactate dehydrogenase using the NADH-imprinted polymer film. 相似文献
10.
Maya Ramesh 《Journal of organometallic chemistry》2004,689(8):1425-1430
The molecular box [CpCo(CN)3]4[Cp*Ru]4 (Co4Ru4) reacts readily with a variety of monocations to form M⊂Co4Ru4+ (M=K+, Cs+, Rb+). Ion competition experiments, monitored by ESI-MS, show that the molecular box binds the smaller K+ more rapidly than Cs+, but that thermodynamically Co4Ru4 prefers the larger ion. The rates of ion-insertion for K+ and Cs+ into Co4Ru4 were found to qualitatively follow second order kinetics with K+, 300 M−1 s−1 and Cs+, 36 M−1 s−1. The ratio kK/kCs qualitatively matched the ESI-MS results from ion competition experiments. The rates of ion-insertion into Co4Ru4 were found to depend on the counter anions. In particular, RbBF4 reacted with Co4Ru4 more slowly than did RbOTf. The slower rates allowed us to establish second order kinetics. 1H NMR studies reveal that the Cp signal for Co4Ru4 is very sensitive to the presence of entering ions, e.g., Rb+, whereas the corresponding Cp signal for Rb⊂Co4Ru4+ was insensitive to the presence of Rb+. The molecular structures of [Co4Ru4] · 6MeCN, [K⊂Co4Ru4]BF4 · 7MeCN, [Cs⊂Co4Ru4]BF4 · 6MeCN and [Tl⊂Co4Ru4]BF4 · 6MeCN, determined by X-ray diffraction, showed that although the compounds crystallized in the same space group I23, a correlation exists between the Ru-N/Co-C bond distances and the size of the interstitial ion. 相似文献