排序方式: 共有179条查询结果,搜索用时 15 毫秒
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Graphene quantum dot-β-cyclodextrin modified glassy carbon electrode was used as a new nanosensor for determination of L-tyrosine (L-Tyr). It was found that graphene quantum dot-β-cyclodextrin has been stably electrodeposited on glassy carbon electrode modified by simple technique. The cyclic voltammograms of the modified electrode in an aqueous solution displayed a pair of well-defined, stable and irreversible reductive/oxidation redox systems. The apparent electron transfer rate constant (ks) and transfer coefficient (α) determined by cyclic voltammetry were approximately equal to 8.0 s–1 and 0.7, respectively. The modified electrode showed excellent catalytic activity towards the oxidation of L-Tyr at positive potential in buffer solution. The nanosensor also displayed fast response time, high sensitivity, low detection limit and a remarkably positive potential oxidation of L-Tyr that decreased the effect of interferences in analysis. 相似文献
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Shahnaz Rostamizadeh Ali Mohammad Amani Reza Aryan Hamid Reza Ghaieni Nasrin Shadjou 《合成通讯》2013,43(20):3567-3576
A simple, inexpensive, and efficient one-pot synthesis of 2,3-dihydroquinazoline-4(1H)-one derivatives under solvent-free conditions using a catalytic amount of iodine with excellent product yields is reported. This methodology provides easy, quantitative access to various 2,3-dihydroquinazoline-4(1H)-one derivatives, using commercially available iodine as a catalyst. 相似文献
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MCM‐41‐SO3H, an ordered mesoporous silica material in which MCM‐41 with covalently anchored sulfonic acid groups was used as an acidic catalyst for the rapid and ‘green’ synthesis of pyrano[3,2‐c]pyridine derivatives under solvent‐free conditions. Reusability of the catalyst, high yields, short reaction times, simplicity and easy workup are advantages of this novel synthetic procedure compared to the conventional methods reported in the literature. 相似文献
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Nasrin Soltani Nahid Tavakkoli Zinat S. Mosavimanesh Fatemeh Davar 《Comptes Rendus Chimie》2018,21(1):54-60
In this study, cyclic voltammetry and differential pulse voltammetry were used to determine the electrochemical properties and concentration of naproxen in pharmaceutical formulation and human serum samples by using a carbon paste electrode modified with activated carbon nanoparticles. Optimum conditions were obtained at an electrode with 0.005 g activated carbon nanoparticles in a phosphate buffer solution of pH 6 as a supporting electrolyte. Linear calibration curves were obtained in the range of 0.1–120 μM, and the detection limit of naproxen determined was 0.0234 μM. The modified electrode shows good selectivity for naproxen in the presence of some organic and inorganic interferences and very good precision in real samples. Finally, naproxen was measured in the presence of acetaminophen. 相似文献
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In the present work, an innovative leach proof nanocatalyst based on dendritic fibrous nanosilica (DFNS) modified with ionic liquid loaded Fe3O4 NPs and CuI salts was designed and applied for the rapid synthesis of imidazo[1,2‐a]pyridines from the reaction of phenyl acetylene, 2‐aminopyridine, and aldehydes in aqueous medium. The structure of the synthesized nanocatalyst was studied by field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), Fourier transform infrared (FT‐IR), flame atomic absorption spectroscopy (FAAS), energy‐dispersive X‐ray (EDX), and X‐ray diffraction (XRD), vapor–liquid–solid (VLS), and adsorption/desorption analysis (Brunauer–Emmett–Teller [BET] equation) instrumental techniques. CuI/Fe3O4NPs@IL‐KCC‐1 with high surface area (225 m2 g?1) and porous structure not only exhibited excellent catalytic activity in aqueous media but also, with its good stability, simply recovered by an external magnet and recycled for eight cycles without significant loss in its intrinsic activity. Higher catalytic activity of CuI/Fe3O4NPs@IL‐KCC‐1 is due to exceptional dendritic fibrous structure of KCC‐1 and the ionic liquid groups that perform as strong anchors to the loaded magnetic nanoparticles (MNPs) and avoid leaching them from the pore of the nanocatalyst. Green reaction media, shorter reaction times, higher yields (71–97%), easy workup, and no need to use the chromatographic column are the advantages of the reported synthetic method. 相似文献
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Ramin Ghorbani‐Vaghei Mohammad Ali Zolfigol Nasrin Moshfeghifar Nadiya Koukabi Gholamabbas Chehardoli 《中国化学会会志》2007,54(3):791-794
An efficient method for the oxidative coupling of thiols to their corresponding disulfides by new reagents poly(N‐bromobenzene‐1,3‐disulfonylamide) PBBS , N,N,N′,N′‐tetrabromobenzene‐1,3‐disulfonylamide TBBDA and DABCO‐bromine complex is described. The reaction was applicable to a variety of thiols with high chemoselectivity. 相似文献
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A series of new phosphoramides with general formula RP(O)X2, where R = amino/p‐methylphenoxy and X = amine, were synthesized and characterized by 1H, 13C, 31P nuclear magnetic resonance (NMR), and infrared (IR) spectroscopy and elemental analysis. The 31P{1H} NMR spectra show that among compounds 7–9 containing 2‐, 3‐, and 4‐aminopyridinyl moieties, respectively, the shielding order of the P atom decreases as 7 > 9 > 8 . Also, the structure of compound 7 was determined by X‐ray crystallography. In this structure, repeated noncentrosymmetric dimers are formed by two strong intermolecular N(1)‐H(1N)…N(2) and N(3)‐H(3N)…O(1) hydrogen bonds. Taking into account weak intermolecular C(17)‐H(17C)…N(4), C(17)‐H(17E)…N(4), C(2)‐H(2A)…O(2), and also weak aromatic C—H…C interactions, a three‐dimensional polymeric chain is created in the crystalline network. The density functional theory calculations at B3LYP, B3PW91, and M06 levels using the 6–31+G** basis set were in good agreement with the X‐ray crystallography data. 相似文献
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Masoumeh Taei Foroozan Hasanpour Mohammad Dinari Nasrin Sohrabi Mohammad Sadegh Jamshidi 《中国化学快报》2017,28(2):240-247
In this study,Au nanoparticles/poly 5-[(2-hydroxynaphthalen-l-yl)diazenyl]isophthalic acid film modified glassy carbon electrode(AuNPs/poly(NDI)/GCE) has shown excellent electrocatalytic activity toward the oxidation of adrenaline(ADR),paracetamol(PAC),and tryptophan(Trp).The bare glassy carbon electrode(GCE) fails to separate the oxidation peak potentials of these molecules,while the poly(NDI) film modified electrode can resolve them.Electrochemical impedance spectroscopy(EIS)indicates that the charge transfer resistance of the bare electrode decreases as 5-[(2-hydroxynaphthalen-l-yl)diazenyl]isophthalic acid is electropolymerized on the bare electrode.Furthermore,EIS exhibits enhancement of electron transfer kinetics between analytes and the electrode after electrodeposition of Au nanoparticles.Differential pulse voltammetry results show that the electrocatalytic current increases linearly in the ranges of 0.01-680.0 μmol L~1 for ADR,0.05-498.0 μmol L~1 for PAC,and 3.0-632.0 μmol L~1 for Trp;with detection limits(S/N = 3) of 0.009 μmol L~1,0.005 μmol L~1,and 0.09 μmol L~1 for ADR,PAC,and Trp,respectively.The proposed method has been successfully applied for simultaneous determination of ADR,PAC,and Trp in biological samples. 相似文献