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121.
Nanomolar Determination of Methyldopa in the Presence of Large Amounts of Hydrochlorothiazide Using a Carbon Paste Electrode Modified with Graphene Oxide Nanosheets and 3‐(4′‐Amino‐3′‐hydroxy‐biphenyl‐4‐yl)‐acrylic Acid
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A novel electrochemical sensor for sensitive detection of methyldopa at physiological pH was developed by the bulk modification of carbon paste electrode (CPE) with graphene oxide nanosheets and 3‐(4′‐amino‐3′‐hydroxy‐biphenyl‐4‐yl)‐acrylic acid (3,′AA). Applying square wave voltammetry (SWV), in phosphate buffer solution (PBS) of pH 7.0, the oxidation current increased linearly with two concentration intervals of methyldopa, one is 1.0×10?8–1.0×10?6 M and the other is 1.0×10?6–4.5×10?5 M. The detection limit (3σ) obtained by SWV was 9.0 nM. The modified electrode was successfully applied for simultaneous determination of methyldopa and hydrochlorothiazide. Finally, the proposed method was applied to the determination of methyldopa and hydrochlorothiazide in some real samples. 相似文献
122.
123.
Zahra Shokri Behzad Zeynizadeh Seyed Ali Hosseini Behrooz Azizi 《Journal of the Iranian Chemical Society》2017,14(1):101-109
Magnetically separable nano core–shell Fe3O4@Cu(OH)x with 22 % Cu content was prepared by the addition of sodium hydroxide to a mixture of CuCl2·2H2O and nano Fe3O4 in water. Characterization of the impregnated copper hydroxide was carried out by X-ray fluorescence (XRF), X-ray diffraction (XRD) atomic absorption spectroscopy (AAS), scanning electron microscopy (SEM), value stream mapping (VSM) and Brunauer–Emmett–Teller (BET) analysis. The core–shell nanocatalyst exhibited the excellent catalytic activity toward reduction of various nitro compounds to the corresponding amines with NaBH4. All reactions were carried out in H2O (55–60 °C) within 3–15 min to afford amines in high to excellent yields. Reusability of core–shell Cu(OH)x catalyst was examined 9 times without significant loss of its catalytic activity. 相似文献
124.
The synthesis of coumarins by hydroxyalkylation of phenols with ethyl acetoacetate (via Pechmann reaction) is attempted using magnetically separable and reusable CuFe2O4 nanoparticles in water.
[Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications ® for the following free supplemental resource(s): Full experimental and spectral details.] 相似文献
125.
Let 𝕂 be a field, and let R = 𝕂[x 1,…, x n ] be the polynomial ring over 𝕂 in n indeterminates x 1,…, x n . Let G be a graph with vertex-set {x 1,…, x n }, and let J be the cover ideal of G in R. For a given positive integer k, we denote the kth symbolic power and the kth bracket power of J by J (k) and J [k], respectively. In this paper, we give necessary and sufficient conditions for R/J k , R/J (k), and R/J [k] to be Cohen–Macaulay. We also study the limit behavior of the depths of these rings. 相似文献
126.
DFT calculations are employed to compare and contrast six-membered ring carbenes including 1,3-dimethyltetrahydropyrimidin-2-ylidene (1a), 1-methyl-3-cyclopropyltetrahydropyridine-2-ylidene (2a), and 1,3-dicyclopropylcyclohexane-2-ylidene (3a) as well as their unsaturated analogues 1b, 2b, 3b, and 2c. The amino groups exert singlet-triplet energy separation (?Es−t) of 60.9 kcal/mol to 1a while cyclopropyls induce a ?Es−t of 14.8 kcal/mol to 3a. The simultaneous presence of amino and cyclopropyl in 2a leads to a ?Es−t of 43.3 kcal/mol. Unsaturation slightly increases the ?Es−t of 1a and 3a but not that of 2a. Our thermodynamic, kinetic, and reactivity results are compared with those of synthetic five-membered ring N-heterocyclic carbenes. 相似文献
127.
Robabeh Baharfar Seyed Meysam BaghbanianSeyed Mohammad Vahdat 《Tetrahedron letters》2011,52(45):6018-6020
The reactive 1:1 zwitterionic intermediate, formed by the addition of isocyanides to dialkyl acetylenedicarboxylates, was trapped by thiouracils to yield a ketenimine intermediate, which cyclized and then rearranged to afford pyrimido[2,1-b][1,3]thiazines in good yields. 相似文献
128.
A fully integrated polydimethylsiloxane (PDMS)/modified PDMS membrane/SU-8/quartz hybrid chip was developed for protein separation using isoelectric focusing (IEF) mechanism coupled with whole-channel imaging detection (WCID) method. This microfluidic chip integrates three components into one single chip: (i) modified PDMS membranes for separating electrolytes in the reservoirs from the sample in the microchannel and thus reducing pressure disturbance, (ii) SU-8 optical slit to block UV light (below 300?nm) outside the channel aiming to increase detection sensitivity, and (iii) injection and discharge capillaries for continuous operation. Integration of all these components on a single chip is challenging because it requires fabrication techniques for perfect bonding between different materials and is prone to leakage and blockage. This study has addressed all the challenges and presented a fully integrated chip, which is more robust with higher sensitivity than the previously developed IEF chips. This chip was tested by performing protein and pI marker separation. The separation results obtained in this chip were compared with that obtained in commercial cartridges. Side-by-side comparison validated the developed chip and fabrication techniques. 相似文献
129.
We report that sodium alginate and its graft-copolymers with (2-dimethylaminoethyl) methacrylate may attach to the surface of colloidal CdS-thioglycerol quantum dots (QDs) via a ligand exchange process and result in water-soluble and highly stable QD supramolecules. Optical properties of modified QDs in water showed that the emission intensity of QDs was still high after surface passivation. 相似文献
130.
Novel method for in-situ surfactant-based solid-phase extraction: application to the determination of Co(II) and Ni(II) in aqueous samples 总被引:1,自引:0,他引:1
We report on a completely new kind of solid phase extraction which we term in-situ surfactant-based solid-phase extraction (ISS-SPE). It represents a simple and rapid method for extraction from aqueous samples and preconcentration of compounds containing hydrophobic (alkyl) groups. A cationic surfactant containing alkyl chain is dissolved in the aqueous sample. Following the addition of hexafluorophosphate (HFP; an ion-pairing anion), solutions turn cloudy due to the interaction between the surfactant and the HFP ion. This is due to the formation of fine solid particles composed of the HFP salt of the cationic surfactant. The alkyl groups of the surfactant in the solid particles strongly interact with hydrophobic groups of analytes and become bound. The solid particles are centrifuged, and the sedimented particles can be either dissolved in an appropriate organic solvent, or leached with a solvent to recover the absorbed analyte(s). The method presented here has distinct advantages in that the extraction times are short and recoveries are high, probably a result of the formation of very fine particles of large specific surface, and of their good dispersion in the sample solution. The performance of ISS-SPE was demonstrated by extracting chelates of Co(II) and Ni(II) from water samples. Under the optimized conditions, the preconcentration factors are 51 and 45, respectively, and the detection limits are 0.9 and 0.6???g?L?1. The method was validated by the analysis of a certified reference material and by comparing results with those obtained by electrothermal AAS. Figure
In ISS-SPE method, a cationic surfactant containing alkyl chain is dissolved in aqueous sample. After addition of hexafluorophosphate anion, a cloudy solution is formed due to formation of fine solid particles (surfactant hexafluorophosphate salt). Hydrophobic anaytes can be adsorbed on the alkyl group of the solid particles and extracted. 相似文献