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91.
New naphtho‐aza‐crown ethers containing different phenolic side‐arms attached through the ortho‐position of the phenol have been prepared under solvent‐free conditions. The starting macrocyclic naphtho‐aza‐crown ether 2 was obtained by treatment of naphthalene dicarboxylic acid diester 1 with diethylenetriamine in EtOH at room temperature for two days without stirring in 77% yield (Scheme 1). Phenolic ligands ( 3 – 14 ) were synthesized by the Mannich reaction of the secondary macrocyclic amine 2 with the substituted phenols using nontoxic and inexpensive CaCl2. This procedure was applied successfully for the synthesis of Mannich bases from simple secondary amines. The CaCl2 powder can be reused up to three times after simple washing with dry acetone. 相似文献
92.
A. M. Hashem A. E. Abdel-Ghany R. El-Tawil A. Bhaskar B. Hunzinger H. Ehrenberg A. Mauger C. M. Julien 《Ionics》2016,22(12):2263-2271
MnO2 nanoneedles (NNs) were synthesized by sol-gel assisted by a redox reaction between ascorbic acid and KMnO4. X-ray powder diffraction (XRD), thermogravimetric analysis (TGA), Raman, far-infrared spectroscopy, and magnetic measurements confirm the tunnel structure of the tetragonal α-MnO2 phase. The MnO2 NNs prepared by sol-gel at moderate temperature (T ≈ 350 °C) aggregate with an urchin-like morphology observed by scanning electron (SEM) and high-resolution transmission electron (TEM) microscopy. Electrochemical investigations show an outstanding initial specific capacity ca. 230 mAh g?1 and 45 % capacity retention at 100th cycle was obtained for these MnO2 nanoneedles. 相似文献
93.
A new titanium complex [Ti(Me–Q)2(Cl)2] (1) is prepared by reacting titanium tetrachloride with 2-methyl-8-hydroxyquinoline in a fast and facile process. The complex is fully characterized based on its 1H and 13C NMR, IR, and UV spectra and elemental analysis. The prepared nanostructured compound is synthesized by the sonochemical method. This new nanostructure is characterized by scanning electron microscopy (SEM), powder X-ray diffraction (XRD), IR spectroscopy, and elemental analysis. Thermal stability of single crystalline and nanosize samples of the prepared compound is studied by thermal gravimetric (TG) and differential thermal analysis (DTA). The prepared complexes both bulk and nanosized are utilized as a precursor for the preparation of TiO2 nanoparticles by direct thermal decomposition at 600°C in air. The morphology and size of TiO2 nanoparticles are determined by SEM, powder XRD, and IR spectroscopy and the results show that the TiO2 nanoparticle size depends on the initial particle size of 1. Photoluminescence (PL) properties of the nanostructured and crystalline bulk prepared complex and their TiO2 nanoparticle cores are investigated. 相似文献
94.
Seyed Mehrdad Jalilian Hassan Farhadnejad Farshid Ziaee Behrouz Furughi Nia Hossein Abdollahi Vahid Najafi 《Polymer Science Series B》2016,58(6):675-680
The free radical solution polymerization of n-octyl methacrylate has been studied in benzene-d 6 in the presence of 2,2′-azobisisobutyronitrile as thermal initiator. An on-line nuclear magnetic resonance spectroscopy was applied to record the reaction data and to determine the monomer conversion at different times during the polymerization reaction. Effect of monomer and initiator concentration as well as reaction temperature on polymerization rate was studied. The order of the reaction with respect to initiator (0.45) was consistent with the classical kinetic rate equation, while the order of reaction with respect to monomer (1.87) was much greater than unity. An overall activation energy (E a = 53.8 kJ/mol) was obtained over the temperature range 328?338 K. Also, the efficiency of the synthesized poly(n-octyl methacrylate) for improving the viscosity index of the lube oil was investigated. 相似文献
95.
Abdol Reza Hajipour Morteza Karimzadeh Sirous Ghorbani Hossein Farrokhpour Alireza Najafi Chermahini 《Structural chemistry》2016,27(5):1345-1362
Electronic structures of allophanic acid were studied using MP2/6-311++G(d,p) level of theory. Five most stable tautomers were selected and stability of them was studied in detail. Obtained data showed that tautomer 1 having hydrogen atom in the central nitrogen N3 and also in a trans conformation of carbonyl and amino functional groups becomes the most stable one. Then, interconversion of these tautomers to each other was investigated step by step through internal rotation and proton transfer routes. Results indicated that movement of protons determines rate-determining step of all paths A–E. Effects of different solvents were carefully surveyed for each tautomer, and among investigated solvents, water made slight stabilization. Activation barrier for proton exchange assisted by one water molecule and one formic acid molecule was also studied, separately. Both molecules had a great influence on lowering barrier especially for proton transfer routes. Comparative MP2 study showed that the barrier will be lowered much more when acid-assisted proton exchange takes place. 相似文献
96.
97.
A. E. Abdel Ghany A. M. A. Hashem H. A. M. Abuzeid A. E. Eid H. A. Bayoumi C. M. Julien 《Ionics》2009,15(1):49-59
Single phase LiCo1 − y
Ni
y
O2 (y = 0.4 and 0.5) with fine particles and high homogeneity was synthesized by “chimie douce” assisted by citric acid as the
polymeric agent and investigated as positive electrodes in rechargeable lithium batteries. The long-range and short-range
structural properties are investigated with experiments including X-ray diffraction (XRD), Fourier transform infrared spectroscopy
(FTIR), and superconducting quantum interference device magnetometry. The physicochemical properties of the powders (crystallinity,
lattice constants, grain size) have been investigated in this composition. The powders adopted the α-NaFeO2 structure as it appeared from XRD and FTIR results. Magnetic measurements shows signal at low temperature attributed to the
magnetic domains in the nanostructure sample from which we estimated that the cation mixing are 3.35 and 4.74% for y = 0.4 and 0.5 in LiCo1 − y
Ni
y
O2, respectively. LiCo0.5Ni0.5O2 cathode yields capacity (135 mAh g−1) compared to LiCo0.6Ni0.4O2 cathode (147 mAh g−1) when discharged to a cutoff voltage of 2.9 V vs. Li/Li+. Lower capacity loss and higher discharge efficiency percentage are observed for the cell of LiCo0.6Ni0.4O2 cathode. 相似文献
98.
A novel model of Cw diode pumped Yb:YAG thin disk laser has been presented to simulate absorption pump power distribution by Monte-Carlo ray tracing. Comparing obtained results with the common distribution function indicate the offered model is quite trustful. So these findings help to evaluate temperature distribution due to the 3D finite element analyses (FEA) based on heat conduction equation. To improve our simulation the temperature dependent of crystal property such as the absorption coefficient, thermal conductivity, stimulated emission cross section and Boltzman population factors are considered by a numerical iterative approach. 相似文献
99.
Zirconium oxide (ZrO2) films have been prepared by using ex situ thermal oxidation of sputtered Zr films on glass and silicon substrates. XRD patterns show that a highly monoclinic (111) preferential orientation of ZrO2 phase can be formed with increasing the oxidation temperature. According to XRD patterns in all thermal oxidized samples silicon oxide phase is present as interfacial layer at the Zr (ZrO2) / Si (glass) interface. In the case of silicon substrates, crystallite sizes obtained from ZrO2 peak with higher intensity reveal an increase with substrate temperature. AFM measurement shows on the whole a decrease of average surface roughness with oxidation temperature. The electrical property of the prepared films is investigated by means of four point probe measurement. An abrupt increase of sheet resistivity occurs when the crystallinity of ZrO2 phase enhances at higher temperature. (© 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
100.
Davarani SS Najafi NM Ramyar S Masoumi L Shamsipur M 《Chemical & pharmaceutical bulletin》2006,54(7):959-962
Electrochemical oxidation of catechol and some 3-substituted catechols (1a--c) has been studied in the presence of 2-chloro-5,5-dimethyl-1,3-cyclohexanedione (3) in aqueous solution using cyclic voltammetry and controlled-potential coulometry. The results indicate that the quinones derived from catechols (1a--c) participate in a Michael addition reaction with 2-chloro-5,5-dimethyl-1,3-cyclohexanedione (3) with consumption of only two electrons per molecule of (1a--c) to from the corresponding benzoforans (10a--c). The electrochemical synthesis of benzofurans has been successfully performed at a carbon rod electrode and in an undivided cell with high yields and purity. 相似文献