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排序方式: 共有1003条查询结果,搜索用时 15 毫秒
1.
In this article we study the well-posedness of the initial value problem for quasi-linear weakly hyperbolic equations of second order. We obtain a sufficient condition for the Cauchy problem to be locally solvable in the class of smooth function. 相似文献
2.
Renato Mario Benazic Tome 《Bulletin of the Brazilian Mathematical Society》1997,28(2):211-231
In this paper, the desingularization problem for an absolutely isolated singularity of an-dimensional holomorphic vector field is solved. Also, we exhibit final forms under blowing-up for this type of singularities. 相似文献
3.
We introduce a family of matrices that define logics in which paraconsistency and/or paracompleteness occurs only at the level of literals, that is, formulas that are propositional letters or their iterated negations. We give a sound and complete axiomatization for the logic defined by the class of all these matrices, we give conditions for the maximality of these logics and we study in detail several relevant examples. (© 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
4.
Domenico Spinelli Giovanni Consiglio Renato Noto 《Journal of heterocyclic chemistry》1977,14(8):1325-1329
The rates of piperidino substitution of some 2-L-3-nitrothiophenes (I) and 2-L-5-nitrothiophenes (II) (L = Cl, Br, I, OC6H4NO2-p, and SO2Ph) have been measured in methanol and in benzene at various piperidine concentrations. The reactivity of compounds (I) is not affected by the piperidine concentration in both methanol and benzene, except for the case of L = I (Ic). Probably due to association effects, the reactivity of Ic in benzene decreases as the piperidine concentration is increased. The reactions of compounds II follow overall second order kinetics in methanol while in benzene a different behaviour is observed as a function of the nature of the leaving group. In fact, the piperidino substitutions of IIa-c (L = Cl, Br, I) are mildly accelerated at high piperidine concentrations (a moderate solvent effect); on the contrary the reactivity of IId and e shows a strong dependence on the piperidine concentration, pointing out a genuine base catalysis. 相似文献
5.
Pau Bernadó Renato Barbieri Esteve Padrós Claudio Luchinat Miquel Pons 《Journal of the American Chemical Society》2002,124(3):374-375
Addition of Tb3+ to purple membrane (PM) suspensions changes the orientation of the menbrane normal from parallel to perpendicular with respect to the magnetic field. Residual dipolar couplings measured in protein L in the presence of PM are scaled by a factor of -1/2. NMR line broadening and cross-correlation effects induced by the addition of PM are partially reversed by Tb3+ but not by Tm3+ that has no effect on the orientation of PM. This is interpreted as the result of anisotropically restricted motion of protein L in the transiently PM-bound form. 相似文献
6.
The hydride transfer process between the isoalloxazine moiety of flavins and the nicotinamide moiety of NAD(P)H has been explored by using density functional theory based reactivity index in the 1-methylnicotinamide-lumiflavine model system. Based on crystallographic data available, we have found that the group softness index helps to locate and orientate reactive regions in these interacting molecules while the electrophilicity index successfully describes the reactivity pattern of this system. 相似文献
7.
Piero Zanello Renato Seeber Bruno Crociani Marino Nicolini 《Transition Metal Chemistry》1980,5(1):45-48
Summary The electrochemical behaviour of a series of cationic platinum(II) isocyanide complexes has been studied in acetonitrile. All the tested compounds are oxidized at a platinum electrode via a two-electron process and reduced at a platinum or mercury electrode via two successive one-electron steps. The anodic step involves the formation of platinum(IV) complexes. The main reduction product formed in correspondence to the first cathodic process is a stable dimer platinum(I) containing bridging isocyanide ligands. Platinum(0) species are formed in the subsequent reduction step. 相似文献
8.
Michelangelo Gruttadauria Renato Noto Serena Riela 《Journal of heterocyclic chemistry》1998,35(4):865-869
The stereoselective synthesis of a 2-substituted tetrahydropyran with adjacent alkoxy-bearing stereogenic centre is described. The key steps of this synthesis were the stereoselective epoxidation of an allylic alcohol and the regioselective epoxide ring opening by lithium aluminum hydride. The regio and stereoselective synthesis of a trihydroxyselenide and a trihydroxysulfide is also described. The latter compounds are not suitable for cyclization to tetrahydrofuran ring. 相似文献
9.
D. Tonelli Renato Seeber Claudio Ciavatta Carlo Gessa 《Analytical and bioanalytical chemistry》1997,359(7-8):555-560
Fractions of humic acids, resolved by ultrafiltration of extracts from a sample of peat treated with alkaline pyrophosphate
solution, have been submitted to high-performance size-exclusion chromatography, with the aim of determining the molecular
weight distributions. Anomalous peaks, located at retention volumes higher than those corresponding to the main signal, are
present in the elution profiles relative to the lightest fractions. These peaks are more intense when using a refractive index
detector rather than a UV detector. Elemental analysis data for the lightest fractions suggested that the spurious peaks are
due to the presence of inorganic material. The hypothesis that pyrophosphate interacts with humic acids in the course of the
extraction has been confirmed by colorimetric determination of the phosphorus content in the different fractions. As a consequence,
the extraction procedure has been modified by using 0.1 mol/L NaOH as extractant.
The average molecular weights of the various fractions, following NaOH extraction, result in substantial agreement with those
obtained following pyrophosphate solution extraction (if the ‘pyrophosphate peaks’ present in the chromatographic profile
are discarded in the calculations).
Received: 18 November 1996 / Revised: 18 February 1997 / Accepted: 23 February 1997 相似文献
10.
Vilar RB da Silva R Schossler P Cataluña Veses R Piatnicki C Samios D Caramão EB 《Journal of chromatography. A》2003,985(1-2):367-373
This work reports preliminary studies on the characterisation of anhydrous ethanol (AEA) used as an automotive fuel mixed with gasoline in Porto Alegre (South Brazil). Pre-concentration of the impurities contained in 1000 ml of AEA was carried on through solid-phase extraction using XAD4 resin. The main compounds in the extract were identified by means of spectral data from the library of the equipment. The concentrate was then fractionated using a preparative liquid chromatographic column filled with activated silica gel and the elution procedure was carried out with, n-hexane, n-hexane-benzene (1:1, v/v) and dichloromethane. Prior to analysis by GC-MS, each fraction was reduced to 1 ml with a gentle stream of nitrogen. Saturated linear hydrocarbons and aromatic hydrocarbons eluted in the first fraction and oxygenated compounds such as aldehydes. ketones and alcohols, eluted in the second one. were the main compounds detected in the sample. 相似文献