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131.
Wilson in 1972 gave a generalization of Arrow's theorem without the Pareto axiom. We prove a version of Wilson's theorem for consensus functions on hierarchies. 相似文献
132.
Boris A. Trofimov Lyubov'' N. Sobenina Zinaida V. Stepanova Tamara I. Vakul''skaya Ol''ga N. Kazheva Grigorii G. Aleksandrov Oleg A. Dyachenko Al''bina I. Mikhaleva 《Tetrahedron》2008,64(23):5541-5544
The solvent-free interaction of 2-phenylpyrrole with bromobenzoylacetylene (room temperature) upon their grinding with solid metal oxides (MgO, CaO, ZnO, BaO, Al2O3, TiO2, ZrO2) and salts (CaCO3, ZrSiO4) leads to either the cross-coupling product or the adduct of pyrrole addition to the riple bond of acetylene. The ethynylation is accompanied by the formation of intermediate and side products: E-2-(1-bromo-2-benzoylethenyl)-5-phenylpyrrole and 1,1-di(5-phenylpyrrol-2-yl)-2-benzoylethene. The activity of the metal oxides in the ethynylation reaction falls in the order (in the brackets, the content of 2-benzoylethynyl-5-phenylpyrrole in the reaction mixture is given): ZnO (81%), BaO (73%), Al2O3 (71%), MgO (69%), CaO (50%). The oxides, SiO2, TiO2, ZrO2, and the salts, CaCO3 and ZrSiO4, are inactive in the ethynylation reaction affording only the intermediate adduct, with ZrO2 the isolated yield of the bromoethenylpyrrole reaching 60%. ESR monitoring shows the reaction to start from one electron transfer from pyrrole to acetylene mediated by the oxide surface. The adduct is readily converted on Al2O3 to 2-(benzoylethynyl)-5-phenylpyrrole crystallized mostly as cis-rotamer (X-ray data). 相似文献
133.
Tamara A. Vaganova Vladimir I. Rodionov Georgij E. Sal’nikov Evgenij V. Malykhin 《Journal of fluorine chemistry》2008,129(4):253-260
Monoamination of octafluoronaphthalene by liquid ammonia affords 2-aminoheptafluoronaphthalene mainly (isolated yield 85-90%). Diamination of octafluoronaphthalene or amination of 2-aminoheptafluoronaphthalene affords a mixture of isomeric 1,6-, 1,7-, 2,6-, and 2,7-diaminohexafluoronaphthalenes with considerable prevalence of the 2,7-isomer (∼70%), thus being the first example of the predominant substitution at position 7 in 2-substituted polyfluoronaphthalenes. The 2,7/2,6 ratio of 2-X-heptafluoronaphthalene (X = −NH, NH2 and NHAc) amination diminishes with the decrease of electron-donating effect of the substituent; 2,7-diaminohexafluoronaphthalene forms in the reactions of 2-aminoheptafluoronaphthalene or octafluoronaphthalene with excess of NaNH2 in liquid ammonia and 2,6-diaminohexafluoronaphthalene—in the reaction of 2-acetylamidoheptafluoronaphthalene with liquid ammonia followed by acetylamido group hydrolysis. The method of the selective preparation of these diamines based on the reversible transformation of amino group and a convenient technique of their high purity isolation by complexation with crown ether have been elaborated. 相似文献
134.
Isabel C.F. Damin Morgana B. Dessuy Tamara S. Castilhos Márcia M. Silva Maria Goreti R. Vale Bernhard Welz Dmitri A. Katskov 《Spectrochimica Acta Part B: Atomic Spectroscopy》2009
The determination of trace elements in crude oil is difficult due to the complex nature of the sample and the various different chemical forms in which the metals can occur. The advantage of graphite furnace atomic absorption spectrometry is that only a minimum of sample pretreatment is required. In this work two techniques have been compared to establish a fast and reliable method for lead determination in crude oil. In the first one the crude oil samples were weighed directly onto solid sampling (SS) platforms and introduced into the graphite tube for analysis. In the second one the samples were prepared as oil-in-water emulsions and analyzed in a filter furnace (FF). Twenty μL of a mixture of 0.5 mg L− 1 Pd + 0.3 mg L− 1 Mg + Triton X-100 has been used as the modifier, and calibration against aqueous solutions has been used for both methods. The sensitivity obtained with the FF was more than a factor of two better than that with SS; however, as a larger sample mass could be introduced in the latter case, so that the limits of detection for both techniques were 0.004 mg kg− 1. Seven crude oil samples were analyzed using the two procedures, and all results were in agreement at a 95% confidence level using a paired Student's t-test. For validation purposes, three crude oil samples have been mineralized using an open-vessel acid digestion, and the results were in agreement with those found with direct sampling and with emulsion sampling using FF according to ANOVA test. Both methods are simple, fast and reliable, being appropriated for routine analysis; however, the direct method using SS technology should be preferred because of its simplicity, speed and commercial availability. 相似文献
135.
Campos Giménez E Trisconi MJ Kilinc T Andrieux P 《Journal of AOAC International》2010,93(5):1494-1502
A fast and simple chromatographic method to determine biotin in foods is presented. Biotin is extracted using papain (60 degrees C, 1 h). After pH adjustment and filtration, biotin is determined by LC with fluorescence detection using postcolumn reagent avidin-FITC (avidin labeled with fluorescein isothiocyanate). The method has been validated in a large range of products: milk- and soy-based infant formulas, cereals, cocoa-malt beverages, and clinical nutrition products. The method showed recovery rates of 98.1 +/- 5.7% (average +/- SD) in a large range of concentrations. Biotin concentrations determined in infant formula standard reference materials 1846 and 1849 were in agreement with reference values. RSD of repeatability (RSDr) varied from 2.0 to 4.5%, and intermediate reproducibility (RSD(iR)) from 5.8 to 9.4%. LOD and LOQ were 3.0 and 5.0 microg/100 g, respectively. The proposed method is suitable for routine analysis of biotin in fortified foods (infant formulas, infant cereals, cocoa-malt beverages, and clinical nutrition products). It can be used as a faster, more selective, and precise alternative to the classical microbiological determination, and is easily transferable among laboratories. 相似文献
136.
B. Ibarra-Escamilla O. Pottiez R. Zhou Q. Zhan P. E. Powers E. A. Kuzin J. W. Haus 《Laser Physics》2011,21(11):1936-1940
We experimentally demonstrated a stable, wavelength-tunable fiber laser using a polarization-maintaining, double-clad Er:Yb
doped fiber amplifier in the cavity. The output wavelength is tunable over the range from 1535 to 1567 nm using a fixed grating
and the dichroic mirror placed on a rotational mount; under rotation of the dichroic mirror the tuning ratio of 50 nm/deg
was found. We studied the wavelength tuning range dependence on the amplifier fiber length and achieved a maximal output power
of 850 mW. This configuration can be Q-switched for high peak power and its narrow bandwidth is suitable for nonlinear optics
applications, such as parametric teraherthz generator. 相似文献
137.
Ezhil Jothinathan Kim VanmeenselJef Vleugels Tamara KharlamovaVladislav Sadykov Svetlana PavlovaGeorgia Sourkouni Christian SzepanskiChristos Argirusis Omer Van der Biest 《Solid State Ionics》2011,192(1):419-423
Apatite type rare earth silicates are being extensively studied as electrolyte material for intermediate temperature solid oxide fuel cells (SOFC). In this paper we presents results on synthesis of Al and/or Fe-doped ATLS, the design of compatible anode materials, thermal expansion properties and co-sintering of half-cells from expansion matched materials using the advanced pulsed electric current sintering (PECS) technique. The issues related to the co-sintering of half cells have been addressed successfully by the combined use of nano powders and PECS. 相似文献
138.
Balázs Pogrányi Dr. Tamara Mielke Dr. Alba Díaz-Rodríguez Dr. Jared Cartwright Dr. William P. Unsworth Prof. Gideon Grogan 《Angewandte Chemie (International ed. in English)》2023,62(5):e202214759
A lyophilized preparation of an unspecific peroxygenase variant from Agrocybe aegerita (rAaeUPO-PaDa-I-H) is a highly effective catalyst for the oxygenation of a diverse range of N-heterocyclic compounds. Scalable biocatalytic oxygenations (27 preparative examples, ca. 100 mg scale) have been developed across a wide range of substrates, including alkyl pyridines, bicyclic N-heterocycles and indoles. H2O2 is the only stoichiometric oxidant needed, without auxiliary electron transport proteins, which is key to the practicality of the method. Reaction outcomes can be altered depending on whether hydrogen peroxide was delivered by syringe pump or through in situ generation using an alcohol oxidase from Pichia pastoris (PpAOX) and methanol as a co-substrate. Good synthetic yields (up to 84 %), regioselectivity and enantioselectivity (up to 99 % ee) were observed in some cases, highlighting the promise of UPOs as practical, versatile and scalable oxygenation biocatalysts. 相似文献
139.
Anatoly I. Rusanov Tamara G. Movchan Elena V. Plotnikova 《Molecules (Basel, Switzerland)》2022,27(22)
A spectrophotometric study of the solubilization and aggregation of the Nile red dye (NR) in premicellar and micellar aqueous solutions of sodium dodecyl sulfate (SDS) was carried out. The experiments were conducted both with saturated solutions of NR under conditions of thermodynamic equilibrium of the solution with a dye precipitate, and at a constant concentration of NR in a homogeneous solution. In the first case, it was proved theoretically and verified experimentally that with an increase in the SDS concentration, the NR concentration always increases, and at the limit of low concentrations, the dependence is linear. In both cases, the concentration of NR dimers as a function passes through a maximum in the premicellar region. There are no dimers in the micellar region. The extinction coefficients of NR monomers in SDS solutions were determined both below and above the critical micelle concentration (CMC) of SDS. A solubilization curve with branches for the premicellar and micellar regions was constructed, the intersection of which was used to find the CMC value in the system under study. The state of deep supersaturation of the NR solution in the metastable state upon dilution of the micellar system with water was studied. It was found that, in addition to dimers, molecular aggregates of higher orders were also formed. 相似文献
140.
Nine water-soluble vitamins: [thiamine (B1), ascorbic acid (C), nicotinamide (PP), pyridoxine (B6), calcium pantothenate (B5), folic acid (B9), cyanocobalamin (B12), riboflavin (B2) and biotin (B8)] were separated on a YMC-Pack Pro C18 column (250 mm x 4.6 mm, 5 microm particle size) in a single run with a gradient elution of mobile phase consisting of 0.025% trifluoroacetic acid pH 2.6 (solvent A) and acetonitrile (solvent B). The separation was achieved within 17 min with a flow rate of 0.8 ml min(-1) and the detection was performed at two wavelengths (210 and 275 nm). The calibration graphs plotted with six concentrations of each vitamin were linear with a regression coefficient R2 > 0.995. The method was applied for the quantification of vitamins B1, C, PP, B6, B5, B9 B2 and B8 in polyvitaminated premixes (premixes) used for the fortification of infant nutrition products. The sample preparation involves an aqueous extraction of vitamins and two different samples dilution were used prior the LC-analysis. The specificity of the method was demonstrated by the retention characteristics, UV spectra and by comparing the peak purity with the standard of each vitamin. The repeatability of the method was evaluated at different level of concentrations on 12 premixes and the coefficients of variation (CVr) were below 6.5%. The values of the intermediate precision (CV1) were below 9.6% (n = 6). The concentrations of vitamins found in premixes with our method were comparable to the declared values, since no bias was found between the two sets of results at 95% confidence. The simplicity of the procedure should make it highly desirable for quality control of premixes in the food industry. 相似文献