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1.
Bounds are given on the size of the parameter-space decomposition induced by multiple sequence alignment problems where phylogenetic information may be given or inferred. It is shown that many of the usual formulations of these problems fall within the same integer parametric framework, implying that the number of distinct optima obtained as the parameters are varied across their ranges is polynomially bounded in the length and number of sequences. 相似文献
2.
Summary Standard analysis of multistep methods for ODE's assumes the application of an initialization routine that generates the starting points. Here ak-step method is considered directly as a mappingR
kn
R
n
. It is shown to approximate a mapping which is expressible directly in terms of the flow of the vector field. Some useful properties of that mapping are shown and for strictly stable methods these are applied to the question of invariant circles near a hyperbolic periodic solution. 相似文献
3.
Sharp peaks were observed in the IR spectra of allyl alcohol dimers in the νOH and τOH regions in low-temperature Ar and N2 matrices. In Ar a peak at 3587 cm?1 was found to increase in intensity upon annealing and decrease upon IR irradiation; it is concluded that this peak is due to an OH...π interaction (of a cyclic structure) present in part of the dimers. This is the first time such an interaction and photoprocess have been found for an alcohol in matrices. Also a faster photo-process was found. Confomer changes in the monomers accompany the photoprocess in allyl alcohol dimers. 相似文献
4.
Timo Rager 《Helvetica chimica acta》2004,87(2):400-407
Pre‐irradiation grafting of styrene/divinylbenzene (DVB) onto poly(tetrafluoroethylene‐co‐hexafluoropropylene) (FEP) films from isopropanol (iPrOH) solution was investigated with respect to the effect of irradiation dose, film thickness, cross‐linker concentration, and reaction temperature. A mathematical model was applied to the kinetic curves to extract information on the polymerization rate, the radical‐recombination rate, and the grafting through time. It turned out that the two closely correlated reaction rates for polymerization and radical recombination can be varied over a wide range by changing the irradiation dose, the cross‐linker concentration, and the reaction temperature. On the other hand, the time until the grafting front has progressed to the center of the film is mainly affected by the film thickness and the reaction temperature. The formation of homopolymer in the grafting solution increases steeply with temperature and cross‐linker concentration. 相似文献
5.
[reaction: see text] Nuclear amination of p-hydroquinones with primary aromatic amines was catalyzed by fungal laccases (EC 1.10.3.2) from Trametes spec. and Myceliophthora thermophila. This is the first report of laccase-catalyzed synthesis of aminoquinones. Incubation of two compounds with laccase in the presence of oxygen resulted in the formation of the corresponding monoaminated or diaminated quinones. No hydroquinonoids were formed. Observed differences in the reaction courses for different p-hydroquinones and aromatic amines with different laccases are discussed. 相似文献
6.
Kumar K Michalik D Garcia Castro I Tillack A Zapf A Arlt M Heinrich T Böttcher H Beller M 《Chemistry (Weinheim an der Bergstrasse, Germany)》2004,10(3):746-757
A practical route for the synthesis of new biologically active 5-HT(2 A) receptor antagonists has been developed. In only three catalytic steps, this class of central nervous system (CNS) active compounds can be synthesized efficiently with high diversity. As the initial step, an anti-Markovnikov addition of amines to styrenes provides an easy route to N-(arylalkyl)piperazines, which constitute the core structure of the active molecules. Here, base-catalyzed hydroamination reactions of styrenes with benzylated piperazine proceeded in high yield even at room temperature. After catalytic debenzylation, the free amines were successfully carbonylated with different aromatic and heteroaromatic halides and carbon monoxide to yield the desired compounds in good to excellent yields. The two key reactions, base-catalyzed hydroamination of styrenes and palladium-catalyzed aminocarbonylation of haloarenes/heterocycles, showed tolerance towards various functional groups, thereby demonstrating the potential to synthesize a wide variety of new derivatives of this promising class of pharmaceuticals. 相似文献
7.
Gun Wirtanen Timo Alanko Tiina Mattila-Sandholm 《Colloids and surfaces. B, Biointerfaces》1996,5(6):319-326
Biofilm growth of Bacillus subtilis, Pseudomonas fragi, Pediococcus inopinatus and Listeria monocytogenes was studied on stainless steel surfaces at room and low temperatures to evaluate the results of traditional hygiene measures. The results were compared with those of image analysis of stainless steel surfaces in an epifluorescence microscope. Statistical analyses were carried out to determine the variations between the conventional cultivation swab method, the glycocalyx amount obtained using swabbing, and the values of the areas of the biofilm, slime and cells. As a general rule, old biofilms showed total counts at approximately the same levels as the young biofilm. The results showed that temperature affected the results for all strains except B. subtilis. The strains of Pe. inopinatus and Ps. fragi showed increased attachment at 6°C and L. monocytogenes at 25°C. The biofilm slime was more easily detached than the cells. The results indicated that the traditional swab method is not reliable for the measurement of biofilm formation on surfaces. 相似文献
8.
We describe a route for the polymer supported total synthesis of the cyclic bisbibenzyls of the isoplagiochin type found in liverworts. TentaGel® resins were used as solid support for a sequence involving Suzuki, Wittig and hydrogenation protocols. The polymer linked intermediates could be characterized by HR-MAS NMR. This route is to be extended to the synthesis of small libraries of differently halogenated derivatives. 相似文献
9.
10.
An Experimental Study of the Kinetics of the Reactions of Isopropyl,sec‐Butyl,and tert‐Butyl Radicals with Molecular Chlorine at Low Pressures (0.5–7.0 Torr) in the Temperature Range 190–480 K 下载免费PDF全文
Timo T. Pekkanen Suula L. Arppe Arkke J. Eskola Matti P. Rissanen Raimo S. Timonen 《国际化学动力学杂志》2016,48(12):796-805
In this work, we have measured the rate coefficients of the reactions of isopropyl (propan‐2‐yl), sec‐butyl (butan‐2‐yl), and tert‐butyl (2‐methylpropan‐2‐yl) radicals with molecular chlorine as a function of temperature (190–480 K). The experiments were done in a tubular laminar flow reactor coupled to a photoionization quadrupole mass spectrometer employing a gas‐discharge lamp for ionization. The radicals were homogeneously produced in the reactor by photolyzing suitable precursor molecules with 193‐nm pulsed exciplex laser radiation. The bimolecular rate coefficients were obtained by monitoring the radical decay signals in real time under pseudo–first‐order conditions. The rate coefficients of all three reactions showed negative temperature dependence. The bath gas used in the experiments was helium, and the rate coefficients appeared to be independent of the helium concentrations employed ([2.4–14] × 1016 cm?3) for all three reactions. The rate coefficients of the reactions can be approximated in the studied temperature range by the following parameterizations: We estimate that the overall uncertainties of the measured rate coefficients are ±20%. We were able to observe 2‐chloropropane (i‐C3H7Cl) product for the i‐C3H7● + Cl2 reaction. No products were observed for the other two reactions, and the reasons for this are briefly discussed in the text. 相似文献