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101.
A novel and simple approach for the efficient and rapid synthesis of pyrano[2,3‐c]‐pyrazoleshas been accomplished via the four‐component condensation reaction of malononitrile, hydrazine hydrate, ethyl acetoacetate, and substituted aldehydes using MIL‐53(Fe) metal–organic framework (MOF) as a catalyst in ethanol at room temperature. Recycling studies have shown that the MIL‐53(Fe) can be readily recovered and reused six times without significant loss of its activity. The present protocol offers the advantages including short reaction times, simple workup, high yields, elimination of toxic solvents, no chromatographic purification and recoverability of the catalyst. Also, the catalyst was fully characterized by SEM, EDX, FT‐IR, XRD, TGA and TEM analysis.  相似文献   
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Russian Journal of Electrochemistry - In this paper, the use of a screen printed electrode modified by feather like La3+/ZnO nano-flowers for the determination of sertraline was described. These...  相似文献   
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Nonlinear Dynamics - In this paper, a numerical simulation of an anomalous reaction–diffusion process in two-dimensional space with a nonlinear source term is presented. An efficient and...  相似文献   
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A multicomponent electrochemical sensor, with two nanometer-scale components in sensing matrix/electrode, was used to simultaneous determination of levodopa (LD) and tyramine (TR) in pharmaceutical and diet samples. Multiwall carbon nanotubes (MWCNTs) were used as carbonaceous materials in the electrode construction. 5-amino-3',4'-dimethoxy-biphenyl-2-ol (5ADMB) was used as electron mediator and Pt nanoparticles (nPt) as a catalyst. The 5ADMB catalyzes the oxidation of LD to the corresponding catecholamine, which is electrochemically reduced back to LD. Preparation of this electrode was very simple and modified electrode showed good properties at electrocatalytic oxidization of LD and TR. Using differential pulse voltammetry (DPV), a highly selective and simultaneous determination of LD and TR has been explored at the modified electrode. Differential pulse voltammetry peak currents of LD and TR increased linearly with their concentrations at the ranges of 0.50–100.0 μM and 0.60–100.0 μM, respectively. Also, the detection limits for LD and TR were 0.31 and 0.52 μM, respectively. The electrode exhibited an efficient catalytic response with good reproducibility and stability.  相似文献   
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Herein we report a fluorescent method for sensitive and selective detection of uranyl ions using CdTe quantum dots functionalized with mercaptopropionic acid, which the fluorescence of the quantum dots could be quantitatively quenched through electron transfer mechanism. The detection limit of the method was estimated to be 4 nM, less than the maximum allowed content of 130 nM for uranyl in drinking water defined by the U.S. Environmental Protection Agency. Furthermore, the probe was successfully applied in detection of uranyl ions in real samples, demonstrating its potential practical applications for monitoring of uranyl ions in environment.  相似文献   
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