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981.
Albert Lévai Gábor Tóth Áron Szőllősy Tibor Timár 《Monatshefte für Chemie / Chemical Monthly》1990,121(5):403-411
Summary Arylsulfonyloxy-2,2-dimethyl-2H-chromenes (26–35) have been synthesized by reduction of arylsulfonyloxy-2,2-dimethyl-4-chromanones (6–15) followed by dehydration.
Synthese von Benzopyranderviaten. 15. Mitt.: Darstellung von Arylsulfonyloxy-2,2-dimethyl-2H-chromenen
Zusammenfassung Reduktion von Arylsulfonyloxy-2,2-dimethyl-4-chromanonen (6–15) und anschließende Dehydratisierung liefert Arylsulfonyloxy-2,2-dimethyl-2H-chromene (26–35).相似文献
982.
J. Šňupárek L. Mrkvičková O. Quadrat Z. Walterová P. Bradna 《Colloid and polymer science》2000,278(12):1205-1210
Model ethyl acrylate–methacrylic acid copolymer latices and latices of particles cross-linked by copolymerizing small amounts
of water-soluble N,N′-methylenebisacrylamide were prepared by nonseeded semicontinuous emulsion copolymerization. Dynamic and static light scattering
measurements indicated a slightly higher degree of polydispersity in the case of cross-linked particles, especially in the
initial stages of polymerization. The hydrodynamic volume of the alkalinized particles controlling the viscosity properties
of the dispersions decreased with the time of polymerization and in the case of cross-linked copolymer almost reached a constant
value at about 1 h. The different character of the particle structure was confirmed by differences in particle disintegration
after alkali addition or in the presence of methanol.
Received: 2 February 1999/Accepted: 28 June 2000 相似文献
983.
Kubíček Vladimír Kučová Daria Císarř Prřemysl Burešová Vlasta 《Mikrochimica acta》2003,142(4):273-276
An ion-pair extraction spectrophotometry method was developed for the determination of fenpiverine bromide in tablets. To determine this substance it was necessary to find experimental conditions that would allow eliminating the influence of other components of the tablets. Attention was paid to the fact that a suitable pH of water phase was necessary to achieve high selectivity.Received December 11, 2002; accepted April 24, 2003
Published online July 28, 2003 相似文献
984.
Wege HA Aguilar JA Rodríguez-Valverde MA Toledano M Osorio R Cabrerizo-Vílchez MA 《Journal of colloid and interface science》2003,263(1):162-169
A new methodology capable of providing reliable and reproducible contact angle (theta) data has been employed to study the effect of clinical treatments grinding, acid etching, and deproteinization on medial dentin tissue. It is based on the application of the ADSA-CD algorithm to the determination of low-rate dynamic contact angles, obtained from slowly growing drops, and on contact angle measurement, as well as spreading behavior analysis, during the relaxation of the system (water on treated dentin) after initial drop growth. The theta data obtained were substantially more reproducible than those obtained with classical methods. A net effect of the treatment on theta was found, increasing dentin wettability: theta (polished) >theta (etched) >theta (deproteinized). The spreading rates correlate with the angles and are adequate for the dentin surface characterization. ANOVA and SNK tests show that for advancing contact angles the means corresponding to all treatments are significantly different. In the relaxing phase, mean angle and spreading rates on polished dentin differ significantly from those on etched and deproteinized dentin, but the latter do not differ significantly from each other. 相似文献
985.
[reaction: see text] A new route to oxcarbazepine (Trileptal), the most widely prescribed antiepileptic drug, starting from commercially available 2'-aminoacetophenone and 1,2-dibromobenzene, is reported. The sequentially accomplished key steps are palladium-catalyzed intermolecular alpha-arylation of ketone enolates and intramolecular N-arylation reactions. After several experiments to establish the best conditions for both arylation processes, the target oxcarbazepine is obtained in a satisfactory overall yield, minimizing the number of steps and employing scalable catalytic procedures developed in partially aqueous media. 相似文献
986.
Ruiz-Medina A Ortega-Barrales P Fernández-de Córdova ML Molina-Díaz A 《Journal of AOAC International》2002,85(2):369-374
A simple, rapid, inexpensive, and automated flow-through solid-phase spectroscopic sensing device is proposed for the sequential determination of 2 vitamins: thiamine and ascorbic acid. The vitamins are concentrated on ion-exchange gels, thiamine on Sephadex SP C-25, and ascorbic acid on Sephadex QAE A-25; both solid supports are packed in 2 different flow cells. The absorbance is monitored directly on the solid phase with a double-beam spectrophotometer at 250 nm, without derivatization or additional elution. With the use of 2 carrier/self-eluting solutions (0.1 5M sodium acetate/acetic acid and 0.18M citric acid/K2HPO4) and a sample volume of 1000 microL, the sensor responds linearly in the range of 0.5-15 and 3-50 microg/mL with detection limits of 0.14 and 0.36 microg/mL for thiamine and ascorbic acid, respectively. When the method was applied to synthetic samples and pharmaceutical preparations, precise and accurate values were obtained. 相似文献
987.
A rapid extraction separation of trace amounts of yttrium from strontium with a nitrobenzene solution of sodium dicarbollylcobaltate (NaDCC) and 18-crown-6 in the presence of tetrasodium salt of ethylenediamine-N,N,N",N"- tetraacetic acid (Na4L) in the aqueous phase was developed. The separation factor a(Sr/Y) was substantially higher than 106. This water-nitrobenzene extraction system can be applied for efficient separation of carrier-free 90Y from 90Sr/90Y generator. 相似文献
988.
Raúl Comelli Zunilda Finelli Sergio Canavese Nora Fígoli 《Reaction Kinetics and Catalysis Letters》1995,55(1):171-181
The effect of Mg addition to Pd impregnated silica-alumina catalysts and the behavior of these catalysts in synthesis gas to hydrocarbons transformation have been studied. Measurements of H2 chemisorption and temperature programmed NH3 desorption allow us to consider that Mg addition to Pd containing catalysts increases the Pd dispersity, the support acidity not being modified. The presence of Mg enhances hydrocarbon production. Meanwhile, the hydrocarbon distribution is not modified. A large amount of light alkanes in the reaction products is obtained. 相似文献
989.
A study of method robustness for arsenic speciation in drinking water samples by anion exchange HPLC-ICP-MS 总被引:2,自引:0,他引:2
Day JA Montes-Bayón M Vonderheide AP Caruso JA 《Analytical and bioanalytical chemistry》2002,373(7):664-668
Regulating arsenic species in drinking waters is a reasonable objective, since the various species have different toxicological impacts. However, developing robust and sensitive speciation methods is mandatory prior to any such regulations. Numerous arsenic speciation publications exist, but the question of robustness or ruggedness for a regulatory method has not been fully explored. The present work illustrates the use of anion exchange chromatography coupled to ICP-MS with a commercially available "speciation kit" option. The mobile phase containing 2 mM NaH(2)PO(4) and 0.2 mM EDTA at pH 6 allowed adequate separation of four As species (As(III), As(V), MMAA, DMAA) in less than 10 min. The analytical performance characteristics studied, including method detection limits (lower than 100 ng L(-1) for all the species evaluated), proved the suitability of the method to fulfill the current regulation. Other parameters evaluated such as laboratory fortified blanks, spiked recoveries, and reproducibility over a certain period of time produced adequate results. The samples analyzed were taken from water utilities in different areas of the United States and were provided by the U.S. EPA. The data suggests the speciation setup performs to U.S. EPA specifications but sample treatment and chemistry are also important factors for achieving good recoveries for samples spiked with As(III) as arsenite and As(V) as arsenate. 相似文献
990.
Martínez-Junza V Rizzi A Jolliffe KA Head NJ Paddon-Row MN Braslavsky SE 《Physical chemistry chemical physics : PCCP》2005,7(24):4114-4125
Photophysical studies with semi-rigid, 1, and flexible, 2, donor-bridge-acceptor (D-b-A2+) molecules with D a porphyrin and A2+ a methyl viologen moiety, were performed in neat polar solvents as well as included in surfactant (DTAB) aqueous and in reverse AOT/n-alkane micelles. The micelles acted as nanoreactors for the photoinduced electron transfer reaction upon laser excitation. In spite of the longer lifetime of the charge separated (CS) state in the semi-rigid tetrad 1(ca. 200 ns vs. ca. 100 ns for the flexible dyad 2), the CS formation quantum yield, for example in acetonitrile, was lower for the former (phi(CS) = 0.13) than for the latter (0.58). Comparison of the time-resolved fluorescence data in neat solvent and in the micelles yielded the phi(CS) values in the dilute micellar solutions. Application of laser-induced optoacoustic spectroscopy at various temperatures to 1 dissolved in a polar organic solvent (benzonitrile, BZN) included in aqueous DTAB nanoreactors afforded structural volume changes for the production in hundreds of ps of the CS state upon excitation of a polar molecule. The contraction during CS formation upon excitation of the collapsed conformer in BZN is attributed to the entering of solvent into the open molecular cavity. The opening upon formation of the CS state due to photoinduced electron transfer in the 1 collapsed conformation arises from the repulsion of the two positively charged ends in this state, as previously calculated. Inclusion of 1 in reverse AOT micelles in various n-alkanes also led to a contraction upon excitation, but the data had much more error due to the limited range of variability of the ratio of thermoelastic parameters. The data obtained with the more flexible "supermolecule" 2 showed the predicted large conformation flexibility of these molecules. 相似文献