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排序方式: 共有453条查询结果,搜索用时 78 毫秒
1.
Bonelli Giulio Grassi Alba Tanzini Alessandro 《Letters in Mathematical Physics》2019,109(9):1961-2001
Letters in Mathematical Physics - We propose that the grand canonical topological string partition functions satisfy finite-difference equations in the closed string moduli. In the case of genus... 相似文献
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We analyse some identifiers which can univocally identify hyperbolic components and Misiurewicz points of one-dimensional quadratic maps. After seeing the equivalence among the different identifiers and how to go from one to another, we show which are the best for some specific tasks. Likewise, we present the analytic expressions, some of them shown for the first time in this paper, to calculate these identifiers. Some experimental considerations are taken into account. 相似文献
4.
Polyazido high-nitrogen compounds: hydrazo- and azo-1,3,5-triazine 总被引:13,自引:0,他引:13
Huynh MH Hiskey MA Hartline EL Montoya DP Gilardi R 《Angewandte Chemie (International ed. in English)》2004,43(37):4924-4928
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Sannomiya M Rodrigues CM Coelho RG dos Santos LC Hiruma-Lima CA Souza Brito AR Vilegas W 《Journal of chromatography. A》2004,1035(1):47-51
The methanolic extract of the leaves of the medicinal plant Byrsonima crassa (Malpighiaceae) contain flavonoids with antioxidant activity. They were separated in a preparative scale using high-speed counter-current chromatography. The optimum solvent system used was composed of a mixture of ethyl acetate-n-propanol-water (140:8:80 (v/v/v)) and led to a successful separation between monoglucosilated flavonoids (quercetin-3-O-alpha-L-arabinoside, quercetin-3-O-beta-D-galactoside) and the biflavonoid amentoflavone in only 3.5 h. The purities of quercetin-3-O-alpha-L-arabinoside (95 mg), quercetin-3-O-beta-D-galactoside (16 mg) and the biflavonoid amentoflavone (114 mg) were all isolated at purity over 95%. Identification was performed by 1H NMR, 13C NMR and UV analyses. 相似文献
6.
Matiide Angulo Mercedes Ruiz Montoya Rafael Marin Galvin José Miguel Rodriguez Mellado 《Electroanalysis》1997,9(4):345-349
The electroreductions of the NAD+ model compounds nicotinamide (I), N1-methyl nicotinamide (II), N′-methyl nicotinamide (III) and isonicotinamide (IV) on carbon electrodes have been studied in aqueous media in the pH range 0–12 by linear-sweep cyclic voltammetry (Scheme 1, I-IV). Logarithmic analyses of the reduction peaks were performed by computing the convolution of the current with time as a function of the potential. On the basis of the experimental results it was concluded that the irreversibility of the electron transfers increased when a glassy carbon electrode was used, and this irreversibility being more marked when a plastic formed carbon electrode was employed. The reduction processes occurred with more difficulty on carbon electrodes than on mercury electrodes. Both the reduction and the reoxidation (when occurred) processes changed with respect to those observed on mercury electrodes, being irreversible electron transfers the rate-determining steps in most cases. Thus, for compounds I, II and III at pH < 2 the reductions occurred by the uptake of two electrons and two H+ ions, and the rate determining step was found to be the first one-electron transfer, for I and III, and the irreversible second electron transfer, preceded by the uptake of an H+ ion, for II. At pH>3 the processes consisted of electrodimerization reactions, preceded by the protonation of the heterocyclic nitrogen in cases I and III. The second electron transfer of the electroreduction of IV always appeared irreversible, in contrast with that found for mercury electrodes. 相似文献
7.
A. Alba M. A. Aramendia V. Borau C. Jimenez J. M. Marinas 《Reaction Kinetics and Catalysis Letters》1984,25(1-2):45-50
The reduction of ,-unsaturated (olefin) carbonyl compounds of the type using a 0.75 wt.% Pd catalyst supported on SiO2–AlPO4 (8020 w/w) in a Parr reactor at low hydrogen pressure is reported. Selectivity in the reduction of the C=C bond is 100% in every case, and the nature of the groups A and B affects reaction rate, thus suggesting a 1,4-hydrogen addition mechanism.
, - () , , 0,75 . % Pd, SiO2–AlPO4 (8020 /), . C=C 100% , A B , 1,4- .相似文献
8.
Several on-column sample preconcentration modes--large-volume sample stacking using the EOF pump (LVSEP), LVSEP with anion-selective exhaustive injection (LVSEP-ASEI) and field-amplified sample injection with sample matrix removal using the electroosmotic flow (EOF) pump (FAEP)--were used to analyze some nonsteroidal anti-inflammatory drugs (NSAIDs) by capillary electrophoresis, and then compared. Methanol was the background electrolyte solvent to suppress the EOF. The effect of the type and length of the solvent plug, and the sample injection time were investigated in FAEP to determine the conditions that provided the best response. LVSEP, LVSEP-ASEI, and FAEP improved the sensitivity of the peak area by 100-, 1200-, and 1800-fold, respectively. The methodology developed, in combination with solid-phase extraction (SPE), was applied to the analysis of water samples. 相似文献
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Le Faou JH Suomijärvi T Blumenfeld Y Piattelli P Agodi C Alamanos N Alba R Auger F Bellia G Chomaz P Coniglione R Del Zoppo A Finocchiaro P Frascaria N Gaardhoje JJ Garron JP Gillibert A Lamehi-Rachti M Liguori-Neto R Maiolino C Migneco E Russo G Roynette JC Santonocito D Sapienza P Scarpaci JA Smerzi A 《Physical review letters》1994,72(21):3321-3324