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151.
Catechins (catechin and other derivatives) are naturally occurring flavonoids present in a number of plants and foods. They are also part of numerous nutraceutical formulations because they are believed to have antioxidant, cancer chemo-preventative, anti-inflammatory and antimicrobial properties. The determination of catechins has traditionally been performed by HPLC. However, this methodology is both time and sample intensive and generates large amounts of organic solvent waste. In the current report, an application of MEKC using a PDMS microchip is presented for the analysis of catechins. The system uses pulsed amperometric detection for direct analysis of important naturally occurring catechins. The effect of pH, surfactant concentration, detection potential and signal stability were analyzed. Linear relationships were found between the concentration and peak current, with good stability and limits of detection of 8 [micro sign]M for catechin, epigallocatechin gallate and epicatechin, and 14 [micro sign]M for epicatechin gallate. Optimum conditions were applied to the detection of selected catechins in a commercially available green tea extract nutraceutical and the results were compared to HPLC analysis. The analysis using microchip micellar electrokinetic chromatography and pulsed amperometric detection was completed in 4.5 min, 10 times faster than the HPLC analysis. 相似文献
152.
Anna Lucia C. H. Villavicencio Jorge Mancini-Filho Henry Delince 《Radiation Physics and Chemistry》2000,57(3-6):295-298
Based on the enormous potential for food irradiation in Brazil, and to ensure free consumer choice, there is a need to find a convenient and rapid method for detection of irradiated food. Since treatment with ionising radiation causes DNA fragmentation, the analysis of DNA damage might be promising. In this paper, the DNA Comet Assay was used to identify exotic meat (boar, jacaré and capybara), irradiated with 60Co gamma rays. The applied radiation doses were 0, 1.5, 3.0 and 4.5 kGy. Analysis of the DNA migration enabled a rapid identification of the radiation treatment. 相似文献
153.
Jan P. Weyrauch Dr. A. Stephen K. Hashmi Prof. Dr. Andreas Schuster Dipl.‐Chem. Tobias Hengst Dipl.‐Chem. Stefanie Schetter Anna Littmann Dipl.‐Chem. Matthias Rudolph Dr. Melissa Hamzic Dr. Jorge Visus Jan W. Bats Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(3):956-963
The substrate scope, the mechanistic aspects of the gold‐catalyzed oxazole synthesis, and substrates with different aliphatic, aromatic, and functional groups in the side chain were investigated. Even molecules with several propargyl amide groups could easily be converted, delivering di‐ and trioxazoles with interesting optical properties. Furthermore, the scope of the gold(I)‐catalyzed alkylidene synthesis was investigated. Further functionalizations of these isolable intermediates of the oxazole synthesis were developed and chelate ligands can be obtained. The use of Barluenga’s reagent offers a new and mild access to the synthetically valuable iodoalkylideneoxazoles from propargylic amides, this reagent being superior to other sources of halogens. 相似文献
154.
Elisa Barea Dr. Giulia Tagliabue Wen‐Guo Wang Dr. Manuel Pérez‐Mendoza Dr. Laura Mendez‐Liñan Francisco J. López‐Garzon Prof. Simona Galli Dr. Norberto Masciocchi Prof. Jorge A. R. Navarro Prof. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(3):931-937
The novel coordination polymers [Cu(Hoxonic)(H2O)]n ( 1 ) and [Cu(Hoxonic)(bpy)0.5]n ? 1.5 n H2O ( 2?H2O ) (H3oxonic: 4,6‐dihydroxy‐1,3,5‐triazine‐2‐carboxylic acid; bpy: 4,4′‐bipyridine) have been isolated and structurally characterised by ab initio X‐ray powder diffraction. The dense phase 1 contains 1D zig‐zag chains in which Hoxonic dianions bridge square‐pyramidal copper(II) ions, apically coordinated by water molecules. On the contrary, 2?H2O , prepared by solution and solventless methods, is based on 2D layers of octahedral copper(II) ions bridged by Hoxonic ligands, further pillared by bpy spacers. The resulting pro‐porous 3D network possesses small hydrated cavities. The reactivity, thermal, magnetic and adsorptive properties of these materials have been investigated. Notably, the adsorption studies on 2 show that this material possesses unusual adsorption behaviour. Indeed, guest uptake is facilitated by increasing the thermal energy of both the guest and the framework. Thus, neither N2 at 77 K nor CO2 at 195 K are incorporated, and CH4 is only minimally adsorbed at 273 K and high pressures (0.5 mmol g?1 at 2500 kPa). By contrast, CO2 is readily incorporated at 273 K (up to 2.5 mmol g?1 at 2500 kPa). The selectivity of 2 towards CO2 over CH4 has been investigated by means of variable‐temperature zero coverage adsorption experiments and measurement of breakthrough curves of CO2/CH4 mixtures. The results show the highly selective incorporation of CO2 in 2 , which can be rationalised on the basis of the framework flexibility and polar nature of its voids. 相似文献
155.
Jorge Antonio Guerrero‐Álvarez Wendy Paloma Mas‐Ku Cesar Garcías‐Morales Armando Ariza‐Castolo 《Magnetic resonance in chemistry : MRC》2010,48(5):356-361
The relative acidities of the cis and trans isomers of a series of 1,5‐oxazaspiro[5.5]undecane derivatives were determined by measuring ΔpK in acid‐base titrations followed by 1 H NMR. Relative structural stabilities were determined by measuring substituent chemical shift and γ‐gauche effects in 13C, 15N, and 17O NMR. Crystallographic characterization of a model spiro[5.5]undecane is presented to support the basicity in solid state. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
156.
157.
Christina M. Gonzalez Jeffrey Hernandez Jason G. Parsons Jorge L. Gardea-Torresdey 《Microchemical Journal》2010,96(2):324-329
Selenium (Se) is naturally occurring in the environment and is an essential nutrient in mammals. However, environmental Se can be increased to toxic levels through different industrial practices. The potential adsorption of the Se oxoanions, selenite and selenate, from aqueous solutions onto nanosynthesized MnFe2O4 was investigated using batch techniques and DRC-ICP-MS spectroscopy. The nanomaterial (NM) was laboratory synthesized through slow titration of a mixture of Fe2+ and Mn2+ ions. X-ray diffraction and Scherrer's equation were used to determine the phase of the material and crystallite size, respectively. The effects of pH, reaction time, competitive anions, and the adsorption capacity of the synthesized NM to bind selenite and selenate were investigated. The Langmuir isotherm was used to determine the binding capacity of the NM. Results showed that the phase of the nanomaterial was similar to Jacobsite with a size of 27.5 nm. Results also showed that the sorption of either 100 ppb of selenite or selenate was pH independent in the pH range 2 to 6 and occurred within 5 min of contact time. The introduction of Cl− and NO3− anions individually added to solution had no significant effect on the sorption of either selenite or selenate. However, it was found that the addition of SO42− had a competitive effect only on the sorption of selenate, first seen at 10 ppm and more pronounced at 100 ppm of SO42−. In the presence of 100 ppm of PO43−, the adsorption of selenate decreased to 87% while selenite sorption decreased to 20%. From the Langmuir isotherm equation it was determined that the nano-Jacobsite had a selenite and selenate binding capacity of 6573.76 and 769.23 mg Se/kg of NM, respectively. 相似文献
158.
CdTe quantum dots (QDs), capped with mercaptopropionic acid (MPA), were synthesized and the variation of their fluorescence properties (steady state and lifetime) with pH was assessed in solution and when immobilized in a sol-gel host. Three different sizes of CdTe QDs with excited state lifetimes ranging from 42 to 48 ns and with emission maximum at 540 nm (QD540), 580 nm (QD580) and 625 nm (QD625) were selected. The solution pH affects the maximum emission wavelength (shifts to higher wavelengths of 23, 24 and 27 nm for QD540, QD580 and QD625, respectively), the excited state lifetime and the fluorescence intensity in a reversible way. Linearization of the maximum emission wavelength variation with the pH allows the estimation of an apparent ionization constant (pKa) for each QD: 6.5 ± 0.1 (QD540), 6.1 ± 0.5 (QD580) and 5.4 ± 0.3 (QD625). The variation of the QDs fluorescence properties was further explored using confocal laser scanning microscopy allowing the implementation of a new calibration method for pH imaging in solution. QDs were successfully immobilized on the tip of an optical fiber by dip-coating using sol-gel procedure. The immobilized QDs showed a similar pH behaviour to the one observed in solution and an apparent lifetime of 80, 68 and 99 ns, respectively. The proposed QDs based methodology can be successfully used to monitor pH using wavelength encoded data in imaging and fiber optic sensing applications. 相似文献
159.
Serxio I. Arias-Barros Antonio Cid Luis García-Río Juan C. Mejuto Jorge Morales 《Colloid and polymer science》2010,288(2):217-221
The influence of different polyethylene glycol (PEG) on the percolation of the ternary system composed by sodium bis(2-ethylhexyl)
sulfosuccinate (AOT) + isooctane + water has been studied. The additives used were chosen on the basis of its chain length
(the number of polymeric units). In all cases, we observed a decrease in the percolation threshold on increasing the amount
of PEG added to the AOT microemulsions. We observed a correlation between the effect exerted by the additive upon the percolation
temperature and its chain length. Moreover, a relationship between the percolation temperature and the additive partition
coefficient between 1-octanol and water (logP) was found. Both of them proved the importance of the inclusion of the additives into the microemulsion interface to explain
their influence upon the percolative phenomenon. Such inclusion modified the properties of the AOT film, facilitating the
exchange of matter between droplets. 相似文献
160.
Carmen Salazar-Hernández Jorge Cervantes Sergio Alonso 《Journal of Sol-Gel Science and Technology》2010,54(1):77-82
The gelation process of TEOS sols in three different solvents using di-n-butyltin dilaurate (DBTL) as polycondensation catalyst has been investigated. Sol compositions were similar to those employed
in the field of stone consolidation for the conservation of historical buildings. Three different systems were studied: TEOS
in ethanol (S-EtOH) which was tested to explain gelation in protic solvents; TEOS in a mixture of methylethylketone/acetone
(S-MA) to represent aprotic solvents; and TEOS in a blend of MEK/ethanol (S-ME) for comparison of a system with properties
intermediate between protic and aprotic solvents. The gelation process was studied by measuring the viscoelastic behavior
near the gelation point (GP). A scaling exponent (Δ) was determined for the elastic modulus, G(ω)′ and the viscous modulus,
G′′(ω), which both follow the same power law, ωΔ, at GP. The fractal dimension, df, was calculated from the scaling exponent, Δ, for each TEOS-DBTL system. For each type
of solvent studied, values of Δ from 0.34 to 0.53 with df of 1.9–2.2 were obtained. The results suggest that DBTL leads to
a TEOS polycondensation mechanism similar to that observed for a base-catalyst system. However, the change in df suggests
that there is a significant effect of the solvent on aggregation mechanisms of the gelation process. A diffusion limited cluster–cluster
aggregation mechanism (DLCCA) was observed when ethanol was used as protic solvent, while a reaction limited cluster–cluster
aggregation mechanism (RLCCA) was observed for MEK/acetone (aprotic solvent). 相似文献