987 resultados para Schiff Bases
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A number of ring-extended DNA adducts resulting from reaction of alpha,beta-unsaturated aldehydes, or their epoxides, with DNA bases have been characterized in recent years. These adducts can lead to miscoding during DNA replication which, if not repaired, result in mutations that can contribute to cancer development. Recently, the use of ultrasensitive methods allowed the detection of background levels of etheno DNA adducts in tissues of untreated animals and humans suggesting the existence of endogenous sources of reactive intermediates. In this review, we briefly summarize the recent advances in the chemistry of these DNA lesions.
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Ultra-trace amounts of Cu(II) were separated and preconcentrated by solid phase extraction on octadecyl-bonded silica membrane disks modified with a new Schiff,s base (Bis- (2-Hydroxyacetophenone) -2,2-dimethyl-1,3-propanediimine) (SBTD) followed by elution and inductively coupled plasma atomic emission spectrometric detection. The method was applied as a separation and detection method for copper(II) in environmental and biological samples. Extraction efficiency and the influence of sample matrix, flow rate, pH, and type and minimum amount of stripping acid were investigated. The concentration factor and detection limit of the proposed method are 500 and 12.5 pg mL-1, respectively.
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Estat del coneixement sobre la neurofisiologia de la consciència, els seus marcs teòrics i els avenços experimentals assolits a finals de 2014.
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In spite of the availability of large databases of chromatographic data on several standardized systems, one major task in systematic toxicological analysis remains, namely how to handle the experimental data and retrieve data from the large available databases in a meaningful and productive way. To achieve this purpose, our group proposed an Internet-based tool using previously published STA databases, which interlaboratorial reproducibility tests have already evaluated. The developed software has the capability to calculate corrected chromatographic parameters, after the input of data obtained with standard mixtures of calibrators, and search the databases, currently incorporating TLC, color reactions, GC and HPLC data. At the end of the process, a list with candidate substances and their similarity indexes is presented.
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Tot seguit presentem un entorn per analitzar senyals de tot tipus amb LDB (Local Discriminant Bases) i MLDB (Modified Local Discriminant Bases). Aquest entorn utilitza funcions desenvolupades en el marc d’una tesi en fase de desenvolupament. Per entendre part d’aquestes funcions es requereix un nivell de coneixement avançat de processament de senyals. S’han extret dels treballs realitzats per Naoki Saito [3], que s’han agafat com a punt de partida per la realització de l’algorisme de la tesi doctoral no finalitzada de Jose Antonio Soria. Aquesta interfície desenvolupada accepta la incorporació de nous paquets i funcions. Hem deixat un menú preparat per integrar Sinus IV packet transform i Cosine IV packet transform, tot i que també podem incorporar-n’hi altres. L’aplicació consta de dues interfícies, un Assistent i una interfície principal. També hem creat una finestra per importar i exportar les variables desitjades a diferents entorns. Per fer aquesta aplicació s’han programat tots els elements de les finestres, en lloc d’utilitzar el GUIDE (Graphical User Interface Development Enviroment) de MATLAB, per tal que sigui compatible entre les diferents versions d’aquest programa. En total hem fet 73 funcions en la interfície principal (d’aquestes, 10 pertanyen a la finestra d’importar i exportar) i 23 en la de l’Assistent. En aquest treball només explicarem 6 funcions i les 3 de creació d’aquestes interfícies per no fer-lo excessivament extens. Les funcions que explicarem són les més importants, ja sigui perquè s’utilitzen sovint, perquè, segons la complexitat McCabe, són les més complicades o perquè són necessàries pel processament del senyal. Passem cada entrada de dades per part de l’usuari per funcions que ens detectaran errors en aquesta entrada, com eliminació de zeros o de caràcters que no siguin números, com comprovar que són enters o que estan dins dels límits màxims i mínims que li pertoquen.
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This article intends to answer the question: "what is the best way to evaluate the strength of acids and bases?" The meaning of the word strength, the main acid-base theories (ionotropic and electron pair), the neutralization reactions and the thermodynamical formalism are considered. Some cases are presented and discussed. In conclusion, evaluating acid-base strength is dependent on the theory (formalism) as well as on the system and measuring techniques.
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Mediante la aplicación de ortesis de silicona, hemos podido reducir y tratar diversas patologías metatarsales de etiologfa biomecánica. Presentamos varios casos clínicos a los cuales mediante la instauración de estos tratamientos ortopodológicos, logramos establecer el comportamiento dinámico del antepié, y reducir las lesiones de partes blandas.
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Water-in-crude oil emulsions are formed during petroleum production and asphaltenes play an important role in their stabilization. Demulsifiers are added to destabilize such emulsions,however the demulsification mechanism is not completely known. In this paper, the performances of commercial poly(ethylene oxide-b-propylene oxide) demulsifiers were studied using synthetic water-in-oil emulsions and model-systems (asphaltenes in organic solvent). No change in the asphaltene aggregate size induced by the demulsifier was observed. The demulsification performance decreased as the asphaltene aggregate size increased, so it can be suggested that the demulsification mechanism is correlated to the voids between the aggregates adsorbed on the water droplets surface.
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Herein, the immobilization of some Schiff base-copper(II) complexes in smectite clays is described as a strategy for the heterogenization of homogeneous catalysts. The obtained materials were characterized by spectroscopic techniques, mostly UV/Vis, EPR, XANES and luminescence spectroscopy. SWy-2 and synthetic Laponite clays were used for the immobilization of two different complexes that have previously shown catalytic activity in the dismutation of superoxide radicals, and disproportionation of hydrogen peroxide. The obtained results indicated the occurrence of an intriguing intramolecular redox process involving copper and the imine ligand at the surface of the clays. These studies are supported by computational calculations.
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The triterpenoids oleanolic (OA) and ursolic (UA) acids show non-selective antiinflamatory activity in vitro for cyclooxygenase (COX) isoforms. 3D conformations of OA and UA, with three possible orientations (1, 1' and 2) in the active site of isoforms COX, obtained by docking, were submitted to molecular dynamics. The results show that orientation 2 of the OA in COX-2 is more favorable because orientation 1 moved away from the active site. The carboxylate group of OA interact by hydrogen bonds with Ser353 and with Phe357 and Leu359, mediated by water, while hydroxyl in C-3 interact by hydrogen bond, mediated by water, with Tyr385.
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This work is part of a study that focused on analyzing the contributions of didactic activities related to scientific language rhetoric characteristics aimed at developing students' abilities to identify such characteristics in chemistry scientific texts and critical reading of those texts. In this study, we present the theoretical basis adopted to determine the scientific discourse characteristics and for the production of the didactic material used in those activities. Latour, Coracini and Campanario studies on persuasive rhetorical strategies present in scientific articles aided the production of such material.
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A simple and fast approach for solid phase extraction is herein described, and used to determine trace amounts of Pb2+ and Cu2+ metal ions. The solid phase support is sodium dodecyl sulfate (SDS)-coated γ-alumina modified with bis(2-hydroxy acetophenone)-1,6-hexanediimine (BHAH) ligand. The adsorbed ions were stripped from the solid phase by 6 mL of 4 M nitric acid as eluent. The eluting solution was analyzed by flame atomic absorption spectrometry (FAAS). The sorption recovery of metal ions was investigated with regard to the effects of pH, amount of ligand, γ-alumina and surfactant and the amount and type of eluent. Complexation of BHAH with Pb2+ or Cu2+ ions was examined via spectrophotometry using the HypSpec program. The detection limit for Cu2+ was 7.9 µg L-1 with a relative standard deviation of 1.67%, while that for Pb2+ was 6.4 µg L-1 with a relative standard deviation of 1.64%. A preconcentration factor of 100 was achieved for these ions. The method was successfully applied to determine analyte concentrations in samples of liver, parsley, cabbage, and water.
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Synthesis, spectral identification, and magnetic properties of three complexes of Ni(II), Cu(II), and Zn(II) are described. All three compounds have the general formula [M(L)2(H2O)2], where L = deprotonated phenol in the Schiff base 2-((z)-(3-methylpyridin-2-yleimino)methyl)phenol. The three complexes were synthesized in a one-step synthesis and characterized by elemental analysis, Fourier transform infrared spectroscopy, electronic spectra, X-ray diffraction (XRD), and room temperature magnetic moments. The Cu(II) and Ni(II) complexes exhibited room temperature magnetic moments of 1.85 B.M. per copper atom and 2.96 B.M. per nickel atom. The X-band electron spin resonance spectra of a Cu(II) sample in dimethylformamide frozen at 77 K (liquid nitrogen temperature) showed a typical ΔMS = ± 1 transition. The complexes ([M(L)2(H2O)2]) were investigated by the cyclic voltammetry technique, which provided information regarding the electrochemical mechanism of redox behavior of the compounds. Thermal decomposition of the complexes at 750 ºC resulted in the formation of metal oxide nanoparticles. XRD analyses indicated that the nanoparticles had a high degree of crystallinity. The average sizes of the nanoparticles were found to be approximately 54.3, 30.1, and 44.4 nm for NiO, CuO, and ZnO, respectively.
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Este trabalho teve por objetivo avaliar o desempenho de mudas da espécie angico-branco (Anadenanthera colubrina (Vell.) Brenan), em condições diferenciadas de disponibilidade de fósforo no solo e de saturação por bases. Os tratamentos foram representados por um fatorial de seis níveis de P (0, 100, 200, 300, 400 e 500 mg/dm³) por cinco níveis de saturação por bases (original = 24, 40, 50, 60 e 70%), sendo dispostos no delineamento em blocos ao acaso, com cinco repetições. Aos 170 dias após a semeadura, foram feitas medições de altura e diâmetro do coleto de todas as plantas, as quais foram colhidas, separadas em raiz e parte aérea e postas a secar para obtenção do peso de matéria seca. A adição da mistura corretiva ao substrato não apresentou resposta significativa por parte da espécie estudada. Essa falta de resposta pode estar relacionada ao fato de que os teores de Ca (0,9 cmol c/dm³) e de Mg (0,4 cmol c/dm³) contidos no solo utilizado tenham sido suficientes para suprir as necessidades das plantas nessa fase. No entanto, observou-se que o angico-branco responde positivamente à aplicação de P. Considerando-se a saturação por bases de 40 e 60%, as doses de P que proporcionaram 90% de produção máxima, com base na produção de matéria seca da parte aérea, foram de 127 e 126 mg/dm³, respectivamente. De acordo com o modelo ajustado para P recuperado, em função do P adicionado, a dose que proporcionará essa disponibilidade de fósforo aos 170 dias é de 976,2 mg/dm³ para V=40% e de 1.277,3 mg/dm³ para V=60%. O nível crítico de P no solo, pelo extrator Mehlich-1, foi de 13,88 mg/dm³ (V=40%) e de 12,87 mg/dm³ (V=60%) e na parte aérea, de 0,14 dag/kg (V=40%) e de 0,12 dag/kg (V=60%).
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O presente trabalho foi desenvolvido com o objetivo de verificar a influência da saturação por bases do substrato sobre o crescimento e a qualidade de mudas de Anadenanthera macrocarpa (angico-vermelho). O delineamento experimental utilizado foi inteiramente casualizado, com quatro repetições por tratamento. Foram empregados três solos como substrato, e para cada um deles a saturação por bases original foi elevada aos seguintes valores: Latossolo Distrófico, 30,0; 50,0; e 70,0%; Latossolo Álico, 25,0; 45,0; e 65,0%; e Argissolo, 50,0; 60,0; e 70,0%. Foram avaliados os parâmetros morfológicos das mudas, suas relações e o índice de qualidade de Dickson. A saturação por bases não teve influência em nenhum dos parâmetros avaliados quando o substrato utilizado foi o argissolo. Exceto no diâmetro do coleto, a elevação da saturação por bases exerceu influência significativa, com padrão linear sobre os parâmetros morfológicos, suas relações e no índice de qualidade de Dickson para mudas produzidas no Latossolo Distrófico. No Latossolo Álico foi observado influência significativa com um comportamento quadrático sobre as características avaliadas, sendo os melhores crescimentos e qualidade encontrados quando a saturação por bases estava próxima de 50,0%.