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991.
992.
993.
This study reports the structural and spectroscopic characterization of a novel metal organic compound formulated as [Fe (bpy)3] [Fe (dipic)2]2.7H2O ( 1 ) (dipic = pyridine‐2,6‐dicarboxylate and bpy = 2,2′‐bipyridine). 1 was investigated by elemental analysis, FT‐IR spectroscopy, powder X‐ray diffraction and single crystal X‐ray diffraction (SC‐XRD), which revealed a triclinic structure of expected composition. Thermal degradation of 1 was also investigated. Complex 1 was used as a precursor to prepare superparamagnetic nanoparticles of Fe3O4 by thermal analysis. The obtained Fe3O4 was characterized by Fourier transformed infrared spectroscopy (FT‐IR), powder X‐ray diffraction (XRD) and scanning electron microscopy (SEM). Fe3O4 nanoparticles were used as a nano‐adsorbent to remove Cd2+ from water at room temperature. The results showed that this nano‐adsorbent is effective in removing Cd2+ from contaminated water sources, and that the maximal effectivity of adsorption occurs at pH = 6. Magnetic measurements of complex 1 and Fe3O4 nanoparticles at room temperature revealed paramagnetic and superparamagnetic behavior, respectively. 相似文献
994.
Kornelija Lasi Ana Bokuli Astrid Mili Biljana Nigovi Ana Mornar 《Biomedical chromatography : BMC》2019,33(8)
This paper presents lipophilicity and bio‐mimetic property determination of 15 phytoestrogens, namely biochanin A, daidzein, formononetin, genistein, genistein‐4,7‐dimethylether, prunetin, 3,4,7‐trihydroxyisoflavon, 4,6,7‐trihydroxyisoflavon, 4,6,7‐trimethoxyisoflavon, daidzin, genistin, ononin, sissotrin, coumestrol and coumestrol dimethylether. High‐performance liquid chromatography with fast gradient elution and Caco‐2 cell line were used to determine the physicochemical properties of selected phytoestrogens. Lipophilicity was determined on octadecyl‐sylane stationary phase using pH 2.0 and pH 7.4 buffers. Immobilized artificial membrane chromatography was used for prediction of interaction with biological membranes. Protein binding was measured on human serum albumin and α‐1‐acid‐glycoprotein (AGP) stationary phases. Caco‐2 assay was used as a gold standard for assessing in vitro permeability. The obtained results differentiate phytoestrogens according to their structure where aglycones show significantly higher lipophilicity, immobilized artificial membrane partitioning, AGP binding and Caco‐2 permeability compared with glucosides. However, human serum albumin binding was very high for all investigated compounds. Furthermore, a good correlation between experimentally obtained chromatographic parameters and in silico prediction was obtained for lipophilicity and human serum albumin binding, while the somewhat greater difference was obtained for AGP binding and Caco‐2 permeability. 相似文献
995.
Jia-Pei Du Dr. Alexander Wilting Prof. Dr. Inke Siewert 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(21):5555-5564
Here, the reduction chemistry of mono- and binuclear α-diimine-Re(CO)3 complexes with proton responsive ligands and their application in the electrochemically-driven CO2 reduction catalysis are presented. The work was aimed to investigate the impact of 1) two metal ions in close proximity and 2) an internal proton source on catalysis. Therefore, three different Re complexes, a binuclear one with a central phenol unit, 3 , and two mononuclear, one having a central phenol unit, 1 , and one with a methoxy unit, 2 , were utilised. All complexes are active in the CO2-to-CO conversion and CO is always the major product. The catalytic rate constant kcat for all three complexes is much higher and the overpotential is lower in DMF/water mixtures than in pure DMF (DMF=N,N-dimethylformamide). Cyclic voltammetry (CV) studies in the absence of substrate revealed that this is due to an accelerated chloride ion loss after initial reduction in DMF/water mixtures in comparison to pure DMF. Chloride ion loss is necessary for subsequent CO2 binding and this step is around ten times faster in the presence of water [ 2 : kCl(DMF)≈1.7 s−1; kCl(DMF/H2O)≈20 s−1]. The binuclear complex 3 with a proton responsive phenol unit is more active than the mononuclear complexes. In the presence of water, the observed rate constant kobs for 3 is four times higher than of 2 , in the absence of water even ten times. Thus, the two metal centres are beneficial for catalysis. Lastly, the investigation showed that the phenol unit has no impact on the rate of the catalysis, it even slows down the CO2-to-CO conversion. This is due to an unproductive, competitive side reaction: After initial reduction, 1 and 3 loose either Cl− or undergo a reductive OH deprotonation forming a phenolate unit. The phenolate could bind to the metal centre blocking the sixth coordination site for CO2 activation. In DMF, O−H bond breaking and Cl− ion loss have similar rate constants [ 1 : kCl(DMF)≈2 s−1, kOH≈1.5 s−1], in water/DMF Cl− loss is much faster. Thus, the effect on the catalytic rate is more pronounced in DMF. However, the acidic protons lower the overpotential of the catalysis by about 150 mV. 相似文献
996.
Hang Yin Qian Cheng Roselyne Rosas Prof. Stéphane Viel Dr. Valérie Monnier Prof. Laurence Charles Prof. Didier Siri Dr. Didier Gigmes Dr. Olivier Ouari Prof. Ruibing Wang Dr. Anthony Kermagoret Dr. David Bardelang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(54):12552-12559
A viologen derivative carrying a benzimidazole group ( V-P-I 2+; viologen–phenylene–imidazole V-P-I ) can be dimerized in water using cucurbit[8]uril (CB[8]) in the form of a 2:2 complex resulting in a negative shift of the guest pKa, by more than 1 pH unit, contrasting with the positive pKa shift usually observed for CB-based complexes. Whereas 2:2 complex protonation is unclear by NMR, silver cations have been used for probing the accessibility of the imidazole groups of the 2:2 complexes. The protonation capacity of the buried imidazole groups is reduced, suggesting that CB[8] could trigger proton release upon 2:2 complex formation. The addition of CB[8] to a solution containing V-P- I 3+ indeed released protons as monitored by pH-metry and visualized by a coloured indicator. This property was used to induce a host/guest swapping, accompanied by a proton transfer, between V-P-I 3+ ⋅ CB[7] and a CB[8] complex of 1-methyl-4-(4-pyridyl)pyridinium. The origin of this negative pKa shift is proposed to stand in an ideal charge state, and in the position of the two pH-responsive fragments inside the two CB[8] which, alike residues engulfed in proteins, favour the deprotonated form of the guest molecules. Such proton release triggered by a recognition event is reminiscent of several biological processes and may open new avenues toward bioinspired enzyme mimics catalyzing proton transfer or chemical reactions. 相似文献
997.
In this study, we present a versatile and easy procedure for modifying a cobalt ferrite nanoparticle step by step. A new nanocatalyst was prepared via CuII immobilized onto CoFe2O4@HT@Imine. The catalyst was fully characterized by Fourier‐transform infrared (FT‐IR), energy‐dispersive X‐ray spectroscopy (EDX), field emission scanning electron microscopy (FE‐SEM), X‐ray diffraction (XRD), and vibrating sample magnetometer (VSM) analyses. The current procedure as a green protocol offers benefits including a simple operational method, an excellent yield of products, mild reaction conditions, minimum chemical wastes, and short reaction times. Without any significant reduction in the catalytic performance, up to five recyclability cycles of the catalyst were obtained. The optimization results suggest that the best condition in the oxidation of benzyl alcohol derivatives is 0.003 g of the CoFe2O4@HT@Imine‐CuII catalyst, TEMPO, at 70°C under solvent‐free condition and air. 相似文献
998.
《Physics letters. A》2019,383(17):2110-2113
The electron effective mass in GaAs quantum wires has been estimated by using a full dynamical random-phase approximation to examine its properties versus spin polarization, temperature, and carrier density. A decrease of mass with spin polarization is seen. The minority mass increases with the polarization while the majority mass decreases and this behaviour is seen for all densities. A maximal enhancement of mass at moderate temperature around 25 K is also presented. These calculations show a qualitative consistence with results in two-dimensional systems and help to control the electronic transport in quantum wires. 相似文献
999.
Zhipeng Lin Hao Zhang Guofeng Liang Yanqi Jin Hongbin Zeng Jiawang Li Jian Chen Weihong Zhang Fangyan Xie Yanshuo Jin Hui Meng 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(12):3112-3118
A composite of FeOOH nanocubes anchored on carbon ribbons has been synthesized and used as a cathode material for Li/O2 batteries. Fe2+ ion-exchanged resin serves as a precursor for both FeOOH nanocubes and carbon ribbons, which are formed simultaneously. The as-prepared FeOOH cubes are proposed to have a core–shell structure, with FeOOH as the shell and Prussian blue as the core, based on information from XPS, TEM, and EDS mapping. As a cathode material for Li/O2 batteries, FeOOH delivers a specific capacity of 14816 mA h g−1cathode with a cycling stability of 67 cycles over 400 h. The high performance is related to the low overpotential of the oxygen reduction/evolution reaction on FeOOH. The cube structure, the supporting carbon ribbons, and the -OOH moieties all contribute to the low overpotential. The discharge product Li2O2 can be efficiently decomposed in the FeOOH cathode after a charging process, leading to higher cycling stability. Its high activity and stability make FeOOH a good candidate for use in non-aqueous Li/O2 batteries. 相似文献
1000.
Chunlai Wu Chuanyun Peng 《International journal of environmental analytical chemistry》2019,99(7):670-682
To develop an accurate and precise method for separation and pre-concentration of Hg(II), a novel thionin functionalised core shell structure magnetic material has been prepared and characterised. The extraction ability of the material was evaluated by magnetic solid-phase extraction coupled with inductively coupled plasma mass spectrometry determination of Hg(II) in food and water samples. Combining the advantages of magnetic separation with selective extraction of thionin towards Hg(II), the material exhibits enhanced enrich selectivity and efficiency for Hg(II). The experimental parameters influencing Hg(II) extraction efficiency, including pH of the aqueous solution, the dosage of the adsorbent, extraction time and sample volume, were systematically investigated. Under the optimised conditions, concentration of Hg(II) at 1.0 μg L?1 can be successfully enriched by the material without the interference of the common co-existing ions. The enrichment factor and adsorption capacity were 250 and 75.2 mg g?1, and precise of the method was confirmed by analysing the spiked food, water samples and standard water reference samples with the recoveries of 92.5–101.8%. 相似文献