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301.
A simple and efficient synthetic protocol has been developed using a one-pot multicomponent reaction (MCR) involving 2-aminophenols, dialkyl acetylenedicarboxylates, and ethyl bromopyruvate in poly(ethyleneglycol). This protocol was utilized to prepare novel pyrrolo[2,1-c][1,4]benzoxazines in excellent yields. 相似文献
302.
Maryam Malekdar Avat Arman Taherpour Issa Yavari Kambiz Larijani 《Structural chemistry》2014,25(5):1483-1493
The reactions on benzotriazoles continue to happen to reach interesting varieties of their derivatives. This study reports a fast one-pot microwave-assisted solvent-free synthesis of N-alkenyl-1,2,3-benzotriazole (3, 5, and 7) and 1-(2-Alkyloxycarbonyl-vinyl)-1H-[1–3] triazole-4-carboxylic acid methyl ester (8 and 9) derivatives by nucleophilic addition reactions of 1,2,3-benzotriazole (C6H5N3) (1) and 1H-[1–3] triazole-4-carboxylic acid methyl ester (C4H4N3O2) (1′) with R-propiolates (R = Me, Et; 2 & 4) and phenylacetylene 6 in good yields. The values of activation energy for rotation around C–N bond in the synthesized N-alkenyl-1,2,3-triazole compounds were studied by DFT-B3LYP/6-31G* method. 相似文献
303.
A new sample preparation method based on microextraction in packed syringe was developed for preconcentration of quercetin prior to its spectrophotometric determination. Molecularly imprinted polymers as packing material was used for higher extraction efficiency. First, glass powder as support material because of low cost and available substrate was modified, and then molecularly imprinted polymers were synthesized by the sol–gel method using 3-aminopropyltriethoxysilane as a functional monomer and tetraethyl orthosilicate as cross-linker agent. The combination of a molecularly imprinted polymers and microextraction in packed syringe increased the selectivity and sensitivity. The surface morphology and functionality of the prepared molecularly imprinted polymers was characterized using Fourier-transform infrared spectroscopy, Field emission scanning electron microscopy, energy dispersive X-ray spectroscopy, and thermogravimetric analysis. Different influencing parameters on extraction efficiency such as effect of the number of sample sorption/desorption cycles, type and volume of desorption solvent, pH of the sample solution, and molecularly imprinted polymers amounts were optimized. Under the optimum condition, the proposed method displayed a linear range from 0.01 to 5 µg mL−1 and limit of detection 3.68 ng mL−1. Relative standard deviation for three replicate determination of 1 µg mL−1 quercetin was 2.1 %. The proposed method was applied successfully for the selective extraction of quercetin from tea and coffee samples. 相似文献
304.
The electrocatalytic reduction of nitrite has been studied by poly(ortho‐toluidine) films modified carbon paste electrode (P‐OT/MCPE). Cyclic voltammetry and chronoamperometry techniques were used to investigate the suitability of poly(ortho‐toluidine) as a mediator for the electrocatalytic nitrite reduction in aqueous solution with various pH. Results showed that pH 0.00 is the most suitable for this purpose. In the optimum pH, the reduction of nitrite occurs at a potential about 600 mV more positive than unmodified carbon paste electrode. The catalytic reaction rate constant, (kh), was calculated 8.68×102 M?1 s?1 by the data of chronoamperometry. The catalytic reduction peak current was linearly dependent on the nitrite concentration and the linearity range obtained was 5.00×10?4 M–1.90×10?2 M. Detection limit has been found to be 3.38×10?4 M (2σ). This method has been successfully employed for quantification of nitrite in real sample. 相似文献
305.
Zhang Z Xiang S Hong K Das MC Arman HD Garcia M Mondal JU Thomas KM Chen B 《Inorganic chemistry》2012,51(9):4947-4953
A three-dimensional triply interpenetrated mixed metal-organic framework, Zn(2)(BBA)(2)(CuPyen)·G(x) (M'MOF-20; BBA = biphenyl-4,4'-dicarboxylate; G = guest solvent molecules), of primitive cubic net was obtained through the solvothermal reaction of Zn(NO(3))(2), biphenyl-4,4'-dicarboxylic acid, and the salen precursor Cu(PyenH(2))(NO(3))(2) by a metallo-ligand approach. The triple framework interpenetration has stabilized the framework in which the activated M'MOF-20a displays type-I N(2) gas sorption behavior with a Langmuir surface area of 62 m(2) g(-1). The narrow pores of about 3.9 ? and the open metal sites on the pore surfaces within M'MOF-20a collaboratively induce its highly selective C(2)H(2)/CH(4) and CO(2)/CH(4) gas separation at ambient temperature. 相似文献
306.
Functionalized poly‐N,N‐dimethylaniline film was prepared by adsorption of ferrocyanide onto the polymer forming at the surface of carbon paste electrode (CPE) in aqueous solution by using potentiostatic method. The electrocatalytic ability of poly‐N,N‐dimethylaniline/ferrocyanide film modified carbon paste electrode (PDMA/FMCPE) was demonstrated by oxidation of cysteamine. Cyclic voltammetry and chronoamperometry techniques were used to investigate this ability. Results showed that pH 7.00 is the most suitable for this purpose. It is found that the catalytic reaction rate constant, (kh), is equal to 2.142×103 M?1 s?1 by the data of chronoamperometry. The catalytic reduction peak current was linearly dependent on the cysteamine concentration and the linearity range obtained was 8.00×10?5 M–1.14×10?2 M. Detection limit was determined 7.97×10?5 M (2σ). This method has been successfully employed for quantification of cysteamine in real sample. 相似文献
307.
Kriti Kapil Dr. Grzegorz Szczepaniak Dr. Michael R. Martinez Dr. Hironobu Murata Dr. Arman Moini Jazani Jaepil Jeong Prof. Dr. Subha R. Das Prof. Dr. Krzysztof Matyjaszewski 《Angewandte Chemie (International ed. in English)》2023,62(10):e202217658
Hyperbranched polymethacrylates were synthesized by green-light-induced atom transfer radical polymerization (ATRP) under biologically relevant conditions in the open air. Sodium 2-bromoacrylate (SBA) was prepared in situ from commercially available 2-bromoacrylic acid and used as a water-soluble inibramer to induce branching during the copolymerization of methacrylate monomers. As a result, well-defined branched polymethacrylates were obtained in less than 30 min with predetermined molecular weights (36 000<Mn<170 000), tunable degree of branching, and low dispersity values (1.14≤Đ≤1.33). Moreover, the use of SBA inibramer enabled the synthesis of bioconjugates with a well-controlled branched architecture. 相似文献