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81.
Mohammad Javad Taghizadeh Hamid ArvinnezhadSaadi Samadi Khosrow Jadidi Abdollah JavidanBehrouz Notash 《Tetrahedron letters》2012,53(38):5148-5150
An efficient, one-pot, three-component procedure for the synthesis of a small library of new chiral spirooxindolopyrrolizidines with high regio-, diastereo-, and enantioselectivity, from the 1,3-dipolar cycloaddition of azomethine ylides and optically active cinnamoyl oxazolidinone is described. The process occurs at room temperature in aqueous ethanol as a green solvent and in the absence of any Lewis acids. The oxazolidinone chiral auxiliary is removed in a non-destructive manner. The reaction mechanism is discussed on the basis of the assignment of the absolute configuration of the cycloadducts, and on theoretical calculations. 相似文献
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85.
Caroline K. Williams Amir Lashgari Nilakshi Devi Marcus Ang Ashwin Chaturvedi Pranita Dhungana Prof. Jianbing Jimmy Jiang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(20):6240-6246
In this work, the electrocatalytic reduction of dichloromethane (CH2Cl2) into hydrocarbons involving a main group element-based molecular triazole-porphyrin electrocatalyst H2PorT8 is reported. This catalyst converted CH2Cl2 in acetonitrile to various hydrocarbons (methane, ethane, and ethylene) with a Faradaic efficiency of 70 % and current density of −13 mA cm−2 at a potential of −2.2 V vs. Fc/Fc+ using water as a proton source. The findings of this study and its mechanistic interpretations demonstrated that H2PorT8 was an efficient and stable catalyst for the hydrodechlorination of CH2Cl2 and that main group catalysts could be potentially used for exploring new catalytic reaction mechanisms. 相似文献
86.
Alireza Bananej Amir Hassanpour Hossein Razzaghi Mehdí Vaez zade Ali Mohammadi 《Optics & Laser Technology》2010,42(8):1187-1192
Monolayer ZrO2 and TiO2 films were prepared on BK7 glass by physical vapor deposition (PVD) and were subsequently annealed for 1 h at 300 °C. By using the transmission spectra of two samples and the envelope method, the refractive index dispersion and extinction coefficients have been calculated. Laser induced damage threshold (LIDT) measurement shows that despite slight differences between the extinction coefficients of the two samples, the LIDT parameter of the ZrO2 film is greater than that of the TiO2 film. This fact leads us to consider thermal conductivity as an important parameter for interpreting the LIDT difference. According to our theoretical analysis, as a consequence of increase in the number of thermal barriers along poorer film, its thermal conductivity, and hence LIDT, decreased, which is in agreement with our experimental results. The measured porosity of the two samples shows higher porosity for TiO2 single layer, which is in agreement with atomic force (AFM) images. The gradual and smooth damage morphology of ZrO2 observed in optical images implies higher thermal conductivity than TiO2. 相似文献
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Hadi Amiri Amir Charkhi Mohammad Ali Moosavian Seyyed Javad Ahmadi Hamed Nourian 《Chemical Papers》2017,71(9):1587-1596
The polydimethylsiloxane (PDMS) mixed matrix membrane with dispersed phase of nanozeolite silicalite-1 has been synthesized on polyethersulphone (PES) as a support, and its performance in the gas separation of xenon and krypton has been studied. For this purpose, nanozeolite silicalite-1 is synthesized by the hydrothermal clear solution method and is characterized by XRD and SEM analysis. In this research, the separation performance of MMM has also been compared with the polymeric PDMS membrane. Furthermore, the effect of feed pressure and loading percentage of nanozeolite in the polymeric matrix are evaluated. The results indicate that the addition of nanozeolite to the polymeric matrix improves its separation performance, and that the changes of the feed pressure have no major effect. The average permeability of the krypton and xenon gases through the PDMS polymeric membrane is calculated as 1.25 × 10?9 and 1.78 × 10?9 cm mol/(cm2 s kPa), respectively, while by adding only 5 wt% of nanosilicalite-1 to the polymeric matrix of the membrane, this amount increased to 1.82 × 10?9 and 8.07 × 10?9 cm mol/(cm2 s kPa), respectively. In addition, the presence of nanosilicalite-1 as the filler leads to an increase in the selectivity of xenon to krypton up to 4.38. 相似文献
89.
Mahdi Tohidian Mohadeseh Nouri Elham Jaafarnia Amir Hossein Haghighi 《Journal of Macromolecular Science: Physics》2015,54(1):17-31
The preparation and characterization of a new type of nanocomposite polyelectrolyte membrane, based on DuPont Nafion/imidazole-modified nanosilica (Im-Si), for direct methanol fuel cell applications is described. Related to the interactions between the protonated imidazole groups, grafted on the surface of nanosilica, and negatively charged sulfonic acid groups of Nafion, new electrostatic interactions can be formed in the interface of Nafion and Im-Si which result in both lower methanol permeability and also higher proton conductivity. Physical characteristics of these manufactured nanocomposite membranes were investigated by scanning electron microscopy, thermogravimetry analysis, differential scanning calorimetry, Fourier transform infrared spectroscopy, water uptake, methanol permeability, and ion-exchange capacity, as well as proton conductivity. The Nafion/Im-Si membranes showed higher proton conductivity, lower methanol permeability and, as a consequence, higher selectivity parameter in comparison to the neat Nafion or Nafion/silica membranes. The obtained results indicated that the Nafion/Im-Si membranes could be utilized as promising polyelectrolyte membranes for direct methanol fuel cell applications. 相似文献
90.
Mehrdad Mahkam Mohammad Galeh Assadi 《Phosphorus, sulfur, and silicon and the related elements》2013,188(4):842-847
A series of acrylic copolymers containing silyl pendant groups was prepared by free radical cross-linking copolymerization. Me3Si, Et3Si, and Ph3Si together with cubane-1,4-dicarboxylic acid (CDA) were covalently linked with 2-hydroxyethyl methacrylate (HEMA). CDA linked to two HEMA group is the cross-linking agent (CA). Free radical cross-linking copolymerization of the methacrylic acid (MAA) and organosilyl monomers with two different molar ratios of CA was carried out at 60–70°C. The compositions of the cross-linked three-dimensional polymers were determined by FT-IR spectroscopy. The glass transition temperature of the network polymers was determined calorimetrically. Equilibrium swelling studies were carried out in enzyme-free simulated gastric and intestinal fluids (SGF and SIF, respectively). A model hydrophobic drug, the steroid hormone estradiol, was entrapped in these gels, and the in vitro release profiles were established separately in both SGF (pH 1) and SIF (pH 7.4). Incorporation of silyl groups in a new macromolecule system modified network polymers for drug delivery. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file. 相似文献