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941.
M. Kooti F. Kooshki E. Nasiri A. Naghdi Sedeh 《Journal of the Iranian Chemical Society》2018,15(4):943-953
In this study, a three-component nanocomposite consisted of graphene, manganese ferrite and phosphotungstic acid (PTA) has been prepared. This composite, which is designated as Graphene/MnFe2O4@PTA, was synthesized through anchoring of PTA–imidazolium ionic liquid on magnetic graphene sheets. The structural and magnetic properties of the fabricated nanocomposite were studied by employing FT-IR, SEM, EDX, TEM, ICP, VSM, P-XRD and BET techniques. The synthesized magnetic nanocomposite was examined as an efficient and recyclable acidic catalyst for Mannich reaction under solvent-free conditions. The products of this reaction, which are an important class of potentially bioactive compounds, were obtained with good to excellent yields, and the catalyst could be readily recycled without any significant loss of its activity. 相似文献
942.
Khalid Mahmoud Hassan 《Journal of the Iranian Chemical Society》2018,15(5):1007-1014
A highly sensitive sensor based on Ni nanoparticles/poly (1,2-diaminoanthraquinone) modified electrode was fabricated at glassy carbon (GC) electrode (Ni/PDAAQ@GC ME) using cyclic voltammetry technique. The incorporation of nickel (II) ions nanoparticles (Ni NPs) followed by anodic polarization process was achieved. Surface morphologies of both PDAAQ@GC ME and Ni/PDAAQ@GC MEs were studied by scanning electron microscope. Ni/PDAAQ@GC ME was tested for simultaneous determination of ascorbic acid (AA), dopamine (DA) and uric acid (UA) by square wave voltammetry technique. The ME showed excellent electrocatalytic activity toward electrooxidation of these biomolecules in their single, binary and ternary systems in alkaline 0.1 M NaOH solutions. Experiment revealed that the low detection limits (LOD) for AA, DA and UA were 0.11, 0.072 and 1.2 µM in single system, respectively, and 0.069, 0.29 and 0.12 µM in ternary system, respectively. 相似文献
943.
Mohammad Ghanbari Neda Mollakarimi Dastjerdi Saman Ahmadi Sanaz Moradi 《Journal of the Iranian Chemical Society》2018,15(5):1119-1131
A novel inorganic–organic nanohybrid material SBA-15@triazine/H5PW10V2O40 (SBA-15@ADMPT/H5PW10V2O40) was prepared and used as an efficient, eco-friendly, and highly recyclable catalyst for the one-pot multicomponent synthesis of multisubstituted pyridines from the reaction of aldehydes, cyclic ketones, malononitrile, and ammonium acetate with good to excellent yields (77–97%). The nanohybrid catalyst was prepared by the chemical anchoring of Keggin heteropolyacid H5PW10V2O40 onto the surface of SBA-15 mesoporous silica modified with 2-APTS -4,6-bis(3,5-dimethyl-1H-pyrazol-1-yl)-1,3,5-triazine (ADMPT) linker. Standard characterization data such as FT-IR, XRD, SEM, TEM, BET, EDX, and DTA-TGA spectroscopy confirmed that the heteropolyacid H5PW10V2O40 is well dispersed on the surface of the solid support and its structure is preserved after immobilization on the SBA-15 mesoporous silica modified with ADMPT. Furthermore, the nanocatalyst can be recovered easily and reused five times without considerable loss of catalytic activity. In general, these advantages highlight this protocol as an attractive and useful methodology, among the other methods reported in the literature, for the eco-friendly and rapid synthesis of biologically active multisubstituted pyridines. 相似文献
944.
Somayeh Hashemi-Uderji Mohammad Abdollahi-Alibeik 《Journal of the Iranian Chemical Society》2018,15(8):1709-1719
A three-component process for the one-pot synthesis of 6-amino-4-aryl-5-cyano-3-methyl-1-phenyl-1,4-dihydropyrano[2,3-c]pyrazoles by the reaction of aldehydes, 3-methyl-1-phenyl-1H-pyrazol-5(4H)-one, and malononitrile in the presence of FSM-16-SO3H as an efficient mesoporous catalyst. The FSM-16-SO3H was prepared and characterized by SEM, XRD, BET, and FT-IR techniques. The advantages of the presented method are high yields, short reaction times, easy purification of products, easy work-up, and reusability of the catalyst. 相似文献
945.
Vitaliy Chagovets Zhihao Wang Alexey Kononikhin Natalia Starodubtseva Anna Borisova Dinara Salimova Igor Popov Andrey Kozachenko Konstantin Chingin Huanwen Chen Vladimir Frankevich Leila Adamyan Gennady Sukhikh 《Journal of the American Society for Mass Spectrometry》2018,29(2):323-330
Recent research revealed that tissue spray mass spectrometry enables rapid molecular profiling of biological tissues, which is of great importance for the search of disease biomarkers as well as for online surgery control. However, the payback for the high speed of analysis in tissue spray analysis is the generally lower chemical sensitivity compared with the traditional approach based on the offline chemical extraction and electrospray ionization mass spectrometry detection. In this study, high resolution mass spectrometry analysis of endometrium tissues of different localizations obtained using direct tissue spray mass spectrometry in positive ion mode is compared with the results of electrospray ionization analysis of lipid extracts. Identified features in both cases belong to three lipid classes: phosphatidylcholines, phosphoethanolamines, and sphingomyelins. Lipids coverage is validated by hydrophilic interaction liquid chromatography with mass spectrometry of lipid extracts. Multivariate analysis of data from both methods reveals satisfactory differentiation of eutopic and ectopic endometrium tissues. Overall, our results indicate that the chemical information provided by tissue spray ionization is sufficient to allow differentiation of endometrial tissues by localization with similar reliability but higher speed than in the traditional approach relying on offline extraction. 相似文献
946.
With the goal of obtaining a water soluble polymeric carrier for preparation of fixed facilitated transport membranes, a water soluble amino containing chitosan derivative was prepared through Michael-addition reaction between chitosan and ethyl acrylate followed by amidation of the ester groups with an appropriate diamine. This derivative was characterized using 1H-NMR spectroscopy. Then, facilitated transport membranes were prepared by casting a thin layer of chitosan derivative/poly(vinyl alcohol) blend on a porous polysolfune support; and the effect of fixed carrier’s content, feed temperature and feed pressure on the CO2 permeance, and CO2/CH4 selectivity of produced membranes were studied. A facilitated transport mechanism for CO2 through this membrane was concluded. 相似文献
947.
Anastasia S. Kondrateva Maxim V. Mishin Sergey E. Alexandrov 《Journal of the American Society for Mass Spectrometry》2017,28(11):2352-2360
NiO layers were deposited by metal-organic chemical vapor deposition using bis-(ethylcyclopentadienyl) nickel (EtCp)2Ni and oxygen or ozone. As a continuation of kinetic study of NiO MOCVD the gas-phase, transformations of (EtCp)2Ni were studied in the temperature range of 380–830 K. Time of reactions corresponding to the residence time of the gas stream in hot zone of the reactor was about 0.1 s under conditions studied. The interaction of (EtCp)2Ni with oxygen started at 450 K and its conversion rate reached the maximum at 700 K. The interaction of (EtCp)2Ni with ozone started at 400 K and its conversion rate reached the maximum at 600 K. Transformations of the gas phase with the temperature in the reaction zone were studied, the model reaction schemes illustrating (EtCp)2Ni transformations in the reaction systems containing oxygen and ozone have developed. In the reaction system (EtCp)2Ni–O2–Ar the main gas-phase products at 380–500 K were CO, CO2, HCO, C2H5OH, CpCOOH, and CpO. Formation of the C2H2O, C3H4O, and C5H8O was found at 630–830 K. The same gas-phase species, (C4H3O)2Ni and dialdehydes was formed in the reaction system (EtCp)2Ni–O3–O2–Ar. 相似文献
948.
Muyi He You Jiang Dan Guo Xingchuang Xiong Xiang Fang Wei Xu 《Journal of the American Society for Mass Spectrometry》2017,28(7):1262-1270
A dual-polarity linear ion trap (LIT) mass spectrometer was developed in this study, and the method for simultaneously controlling and detecting cations and anions was proposed and realized in the LIT. With the application of an additional dipolar DC field on the ejection electrodes of an LIT, dual-polarity mass spectra could be obtained, which include both the mass-to-charge (m/z) ratio and charge polarity information of an ion. Compared with conventional method, the ion ejection and detection efficiency could also be improved by about one-fold. Furthermore, ion–ion reactions within the LIT could be dynamically controlled and monitored by manipulating the distributions of ions with opposite charge polarities. This method was then used to control and study the reaction kinetics of ion–ion reactions, including electron transfer dissociation (ETD) and charge inversion reactions. A dual-polarity collision-induced dissociation (CID) experiment was proposed and performed to enhance the sequence coverage of a peptide ion. Ion trajectory simulations were also carried out for concept validation and system optimization. 相似文献
949.
Jiang Zhang Rachel R. Ogorzalek Loo Joseph A. Loo 《Journal of the American Society for Mass Spectrometry》2017,28(9):1815-1822
Native mass spectrometry (MS) with electrospray ionization (ESI) has evolved as an invaluable tool for the characterization of intact native proteins and non-covalently bound protein complexes. Here we report the structural characterization by high resolution native top-down MS of human thrombin and its complex with the Bock thrombin binding aptamer (TBA), a 15-nucleotide DNA with high specificity and affinity for thrombin. Accurate mass measurements revealed that the predominant form of native human α-thrombin contains a glycosylation mass of 2205 Da, corresponding to a sialylated symmetric biantennary oligosaccharide structure without fucosylation. Native MS showed that thrombin and TBA predominantly form a 1:1 complex under near physiological conditions (pH 6.8, 200 mM NH4OAc), but the binding stoichiometry is influenced by the solution ionic strength. In 20 mM ammonium acetate solution, up to two TBAs were bound to thrombin, whereas increasing the solution ionic strength destabilized the thrombin–TBA complex and 1 M NH4OAc nearly completely dissociated the complex. This observation is consistent with the mediation of thrombin-aptamer binding through electrostatic interactions and it is further consistent with the human thrombin structure that contains two anion binding sites on the surface. Electron capture dissociation (ECD) top-down MS of the thrombin–TBA complex performed with a high resolution 15 Tesla Fourier transform ion cyclotron resonance (FTICR) mass spectrometer showed the primary binding site to be at exosite I located near the N-terminal sequence of the heavy chain, consistent with crystallographic data. High resolution native top-down MS is complementary to traditional structural biology methods for structurally characterizing native proteins and protein–DNA complexes. 相似文献
950.
Marjan Hematyar Ali Es-haghi Majid Soleimani Ali Rezaie Mokarram 《Journal of the Iranian Chemical Society》2017,14(12):2665-2671
In this work, magnetic solid-phase extraction based on sodium dodecyl sulfate-coated Fe3O4 nanoparticles has been successfully applied for extraction and preconcentration of trace amounts of nystatin from water and vaccine samples prior to high-performance liquid chromatography–ultraviolet detection. Various experimental parameters affecting extraction and recovery of the analyte, such as the amount of sodium dodecyl sulfate, pH of the sample solution, salt concentration, extraction time, sample volume and desorption conditions, were systematically studied and optimized. Under optimized conditions, nystatin was quantitatively extracted. Proper linear range with good coefficient of determination, (R 2 > 0.99) and limit of detection and quantification (based on signal-to-noise ratios of 3 and 10) of 2.0 and 5.0 µg L?1, over the investigated concentration range (5–700 µg L?1), were obtained, respectively. The intra-day and inter-day relative standard deviations at 50 µg L?1 level of NYS were 1.4 and 4.5% based on six replicate determinations. The accuracy of the method was evaluated by recovery measurements on spiked samples. Suitable recoveries of 96–102 and 26–44% were achieved (at spiked levels of 50, 300 and 500 µg L?1) for water and vaccine samples, respectively. 相似文献