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181.
Marcos J Pascual JA de la Torre X Segura J 《Journal of mass spectrometry : JMS》2002,37(10):1059-1073
A fast and sensitive method for the comprehensive screening of anabolic agents and other banned doping substances using gas chromatography/tandem mass spectrometry (GC/MS/MS) with an external ionization ion trap mass spectrometer is presented. The method takes advantage of the resolving power of MS/MS to eliminate background interferences, thus speeding up the chromatographic analysis. For each compound, different fragmentation reactions were studied and their collision energies optimized to obtain the best sensitivity in terms of their signal-to-noise ratio (S/N). A dramatic reduction in overall analysis time was achieved compared with other common approaches. More than 50 substances could finally be monitored in less than 7.4 min with detection limits (S/N >3) lower than 0.5 ng ml(-1) for most of the compounds with special sensitivity requirements according to the International Olympic Committee (IOC). A validation procedure for qualitative analysis was performed. The selectivity of the method showed that no interfering peaks were observed at the retention time of the analytes. Good intermediate precision, below 25% for most of the compounds, and robustness were observed. The optimized method was successfully applied to analyse more than 100 real human urine samples with optimum sensitivity and specificity rates. 相似文献
182.
Joaquin Barbera Mercedes Marcos Ana Omenat Jose-Luis Serrano Jesus I. Martinez Pablo J. Alonso 《Liquid crystals》2013,40(2):255-262
The synthesis and liquid crystalline behaviour of the first and second generations of a dendrimeric structure based on poly(propyleneimine)(DAB-dendr(NH2)x) are reported. 4-(4-n-Alkoxybenzoyloxy)salicylaldehydes are used as mesogenic moieties attached at the peripheral amino groups of the dendrimers giving rise to dendromesogens with four and eight mesogenic branches. From these dendromesogens, considered as organic ligands, were prepared six metal-containing dendrimers which incorporate two or four copper atoms in their structures. All the dendrimeric ligands and three of the metal-containing dendrimers exhibit liquid crystalline properties which were studied by optical microscopy, DSC, X-ray diffraction and EPR spectroscopy. 相似文献
183.
Abstract One series of 4-n-octyl-N-(4-X-benzylidene)anilines and two series of polar orthopalladated complexes derived from these of type Pd2(μ-Y)2 p-X-C6H3-CH = N-C6H4-C8H17 2; X: -H, -F, -Cl, -Br, -NO2, -CN, -CH3, -OCH3, -CF3, -COOCH3, -OCOCH3 and -OCOQH5; Y: -OAc and -Cl; have been synthesized and their mesogenic properties studied. In the polar Schiff bases used as organic ligands, the polar end group determines both the presence of the mesophase and the type of mesophase exhibited. In the complexes, however, it is the central structure of the molecule that practically always determines mesogenic behaviour. No acetato-bridged complex is mesogenic. All the chloro-bridged complexes, however, show mesogenic behaviour. All these compounds show smectic A mesophases with the exception of the CN compound, which only exhibits a nematic mesophase. 相似文献
184.
185.
Silva MM Vale MG Damin IC Welz B Mandaji M Fett JP 《Analytical and bioanalytical chemistry》2003,377(1):165-172
The amount of sample that is available for analysis in laboratory plant cultivation experiments is usually very limited. Highly sensitive analytical techniques are therefore required, even for elements that are present in the plants at mg g–1 concentrations, and graphite furnace atomic absorption spectrometry (GFAAS) was chosen in this work because of its micro-sampling capability, and its relatively simple operation. Four micro-methods were investigated for the determination of iron in roots and leaves of rice plants: i) a micro-digestion with nitric and hydrochloric acids, ii) a slurry procedure using tetramethylammonium hydroxide (TMAH) tissue solubilizer, iii) a slurry prepared in 1.4 mol L–1 nitric acid, and treated in an ultrasonic bath, and iv) the direct analysis of solid samples. The micro-digestion was suffering from high blank values and contamination problems, so that it could not be recommended for routine purposes. The TMAH method exhibited poor precision and occasional low recoveries, particularly for real samples. Direct solid sampling analysis gave results similar to those obtained with the slurry technique with ultrasonic agitation for the determination of iron in certified reference materials with iron content up to about 100 g g–1, but was too sensitive for the investigated rice plants, which had an iron content up to several mg g–1. The slurry technique with ultrasonic treatment of the samples, suspended in dilute nitric acid, was finally adopted as the method of choice.The method was then applied for the determination of iron in the leaves and in different compartments of the roots of two rice cultivars, one sensitive to iron toxicity, an important nutritional disorder, and the other one resistant to iron toxicity. The results suggest that the higher resistance to iron toxicity of the second cultivar is due to a smaller uptake of iron from the soil, resulting in lower iron levels in all compartments of the plant. 相似文献
186.
Willian R. Rocha Josefredo R. Pliego Stella M. Resende Hlio F. Dos Santos Marcos A. De Oliveira Wagner B. De Almeida 《Journal of computational chemistry》1998,19(5):524-534
The potential energy surface (PES) for the cyclooctane molecule was comprehensively investigated at the Hartree–Fock (HF) level of theory employing the 3–21G, 6–31G, and 6–31G* basis sets. Six distinct true minimum energy structures (named B, BB, BC, CROWN, TBC, and TCC1), characterized through harmonic frequency analysis, were located on the multidimensional PES. Two transition state structures were also located on the PES for the cyclooctane molecule. Electron correlation effects were accounted for using the Møller–Plesset second-order perturbation theory (MP2) approach. The predicted global minimum energy structure on the ab initio PES for the cyclooctane molecule is the BC conformer. A gas phase electron diffraction study at 300 K suggested a conformational mixture while an NMR study in solution at 161.5 K predicted the BC conformer as the predominant form. The equilibrium constants reported in the present study, which were evaluated from the ab initio calculated total Gibbs free energy change values, were in good agreement with both experimental investigations. The ab initio results showed that the low temperature condition significantly favored the BC conformer while above room temperature both BC and CROWN structures can coexist. © 1998 John Wiley & Sons, Inc. J Comput Chem 19: 524–534, 1998 相似文献
187.
Maíra Fasciotti Gustavo B. Sanvido Vanessa G. Santos Priscila M. Lalli Michael McCullagh Gilberto F. de Sá Romeu J. Daroda Martin G. Peter Marcos N. Eberlin 《Journal of mass spectrometry : JMS》2012,47(12):1643-1647
The use of CO2 as a massive and polarizable drift gas is shown to greatly improve peak‐to‐peak resolution (Rp‐p), as compared with N2, for the separation of disaccharides in a Synapt G2 traveling wave ion mobility cell. Near or baseline Rp‐p was achieved for three pairs of sodiated molecules of disaccharide isomers, that is, cellobiose and sucrose (Rp‐p = 0.76), maltose and sucrose (Rp‐p = 1.04), and maltose and lactose (Rp‐p = 0.74). Ion mobility mass spectrometry using CO2 as the drift gas offers therefore an attractive alternative for fast and efficient separation of isomeric disaccharides. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
188.
The use of aerosol produced in a nebulization chamber is proposed as an alternative to gas sample capture in flow systems. This paper describes the coupling of a sampling interface with a flow system, for in situ gas monitoring. Aspects related with the behavior of aerosol formation and gas solubilization in liquid drops are discussed. The method is applied to the determination of residual lime in acidic soils. Aliquots of 5.0 ml of 1.0 mol l−1 HCl were mixed with soil samples (1 g). The CO2 released from these samples was captured by a nebulized aerosol and determined conductivity. The analytical curve from 1.0×10−2 to 5.0×10−2 mol kg−1 CaCO3 was ploted applying the matrix matching approach. This proposition, allowed an increase in the sensibility with detection limit of 6.0×10−3 mol kg−1. The precision was good (R.S.D. <3%) for an analytical frequency of 22 determinations per hour. A fair agreement, at 95% confidence level, was found between the results from the proposed method and certified values of the investigated samples. 相似文献
189.
This article presents a method that provides the molecular weight distribution (MWD) of polymeric material from rheological data. The technique has been developed to deal with linear polymers with a log‐normal molecular weight distribution. The rheological data must include the shear storage modulus, G′(ω), and the shear loss modulus, G″ (ω), ranging from the terminal zone to the rubberlike zone. It was not necessary to achieve the relaxation spectrums via the extremely unstable problem of inverting integral equations. The method has been tested with different polymers (polydimethylsiloxane, polyisoprene, random copolymer of ethylene and propylene, and polystyrene) and the calculated MWDs were in good agreement with experimental data. © 2000 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 38: 1539–1546, 2000 相似文献
190.
In this paper an enzymatic fluorometric sensor for glucose determination in drinks is presented. The sensor film was obtained by immobilisation of glucose oxidase chemically modified with a fluorescein derivative (GOx-FS) in a polyacrylamide polymer. During the enzymatic reaction the changes in the fluorescence intensity of the GOx-FS are related to the glucose concentration. Working in FIA mode, the optimum conditions found were: 0.7 ml min(-1) flow rate, 300 mul sample injection and pH 6.5. The sensor responds to glucose concentrations ranging from 400 to 2000 mg l(-1), the reproducibility is around 3% and the life-time is at least 3 months (more than 350 measurements). The sensor was applied to direct glucose determination in drinks with good accuracy; interference caused by the filter effect was avoided by the kinetics of the reaction. 相似文献