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11.
A rapid, efficient, convenient and cost-effective procedure has been developed for the synthesis of 3,5-bis-(arylmethylidene)-tetrahydropyran-4-ones by the condensation of tetrahydropyran-4-one with araldehydes in the presence of catalytic amount of iodine to obtain the products in good to excellent yield. The reactions work at 25 °C and go to completion within 30–60 min. 相似文献
12.
Superior laryngeal nerve paresis and paralysis 总被引:1,自引:0,他引:1
Gürsel Dursun Robert Thayer Sataloff Joseph R. Spiegel Steven Mandel Reinhardt J. Heuer Deborah Caputo Rosen 《Journal of voice》1996,10(2):206-211
Superior laryngeal nerve paresis and paralysis are relatively common but often difficult to diagnose with certainty. They are most commonly caused by viral infections, though other etiologies must be considered. A thorough history and physical examination, including strobovideolaryngoscopy and laryngeal electromyography, are needed for definitive diagnosis. It is essential to establish the diagnosis accurately to differentiate an apparent superior laryngeal nerve paresis from other conditions, such as myasthenia gravis. Laryngeal electromyography is used to confirm clinical impressions, as a guide for therapy, and as one measure of recovery. In our experience, accurate and early diagnosis assure the best phonatory outcome by directing therapy that will prevent or eliminate compensatory vocal abuses, which may themselves lead to even more serious vocal injury. 相似文献
13.
Platinum electrodes modified with Mn(II) 5-(N-(8-pyrrole-yl-3,6-dioxa-1-aminooctane)phenylamide-10,15,20-trimethoxyphenylporphyrin (Mn(II)triOMeTCPPyP) using multi-sweep cyclic voltammetry and differential pulse amperometry were evaluated as electrocatalytic surfaces for the oxidation of nitric oxide. The electrodes modified using the pulse amperometric approach were more sensitive towards the detection of nitric oxide. The increased sensitivity led to the attainment of a wider linear dynamic range for the quantification of nitric oxide. 相似文献
14.
A modified electrode was fabricated by electrochemically deposition of Pt nanoparticles on the multiwall carbon nanotube covered glassy carbon electrode (Pt nanoparticles decorated MWCNT/GCE). A higher catalytic activity was obtained to electrocatalytic oxidation of ascorbic acid, dopamine, and uric acid due to the enhanced peak current and well‐defined peak separations compared with both, bare and MWCNT/GCE. The electrode surfaces were characterized by scanning electron microscopy (SEM), X‐ray diffraction (XRD) and electrochemical impedance spectroscopy (EIS). Individual and simultaneous determination of AA, DA, and UA were studied by differential pulse voltammetry. The detection limits were individually calculated for ascorbic acid, dopamine, and uric acid as being 1.9×10?5 M, 2.78×10?8 M, and 3.2×10?8 M, respectively. In simultaneous determination, LODs were calculated for AA, DA, and UA, as of 2×10?5 M, 4.83×10?8 M, and 3.5×10?7 M, respectively. 相似文献
15.
Sonochemical oxidation of benzyl alcohols into corresponding aldehydes by FeCl(3)/HNO(3) in acetone at room temperature has been reported. All substrates give good yield of the products within 10-25 min. The reaction of selected substrates were also studied under reflux and at the room temperature. Further, various Lewis acids were used to evaluate their catalytic efficacy. 相似文献
16.
An expeditious synthesis of 2-aryl-benzimidazoles by the condensation of o-phenylenediamine with various araldehydes is described. This greener protocol is catalyzed by Amberlite IR-120, and proceeds efficiently in the absence of any organic solvent under microwave irradiation within 3–5 min. 相似文献
17.
18.
Salman M. Saadeh Nizam M. El‐Ashgar Issa M. El‐Nahhal Mohamed M. Chehimi Jocelyne Maquet Florence Babonneau 《应用有机金属化学》2005,19(6):759-767
A porous, solid insoluble polysiloxane‐immobilized ligand system bearing pyrogallol active sites of the general formula P? (CH2)3? NH(CH2)3OC6H3(OH)2 (where P represents [Si? O]n siloxane network) has been prepared by the reaction of 3‐aminopropylpolysiloxane with 1,3‐dibromopropane followed by the reaction with pyrogallol. 13C CP‐MAS NMR and X‐ray photoelectron spectroscopy confirmed that the pyrogallol is chemically bonded to the siloxane backbone. Thermal analysis showed that the ligand system is stable under nitrogen at relatively high temperature. The polysiloxane–pyrogallol ligand system exhibits high potential for the uptake of the metal ions (Fe3+, Co2+, Ni2+ and Cu2+). Complexation of the pyrogallol ligand system for the metal ions at the optimum conditions was found to be in the order Fe3+ > Cu2+ > Ni2+ > Co2+. Copyright © 2005 John Wiley & Sons, Ltd. 相似文献
19.
Aluminum is one of the most toxic metals causing a variety of neurologic diseases, especially Alzheimer's disease. It is impossible to avoid contact with aluminum because of its existence in food to medications. Therefore, removal of aluminum from the blood or wastewater is urgently important. The cost-effective and easy-to-prepare adsorbents are needed to get efficient aluminum removal. For that purpose, the poly(2-hydroxyethylmethacrylate-co-acrylic acid), poly(HEMA-co-AA), microparticles was synthesized to remove aluminum in a very short interaction time. The achievement of the desired polymeric structure was confirmed via Fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM) and transmission electron microscope (TEM), etc. Additionally, particle features such as swelling ratio, size, and surface area were determined. The microparticles synthesized in this study have been determined with very good adsorption capacity even in small aluminum concentrations. 相似文献
20.
Özge Dağlı Dursun Ali Köse Onur Şahin Zarife Sibel Şahin 《Journal of Thermal Analysis and Calorimetry》2017,128(3):1373-1383
The coumarilate (coum?) complexes of CoII(1), NiII(2) CuII(3) and ZnII(4) were synthesized and characterized by elemental analysis, magnetic susceptibility, solid-state UV–Vis, FTIR spectra, thermoanalytical TG–DTG/DTA and single-crystal X-ray diffraction methods. It was found that all of the complex structures have 2 mol (coum?) ligand bonded as monoanionic monodentate in the structures of 1 and 2 while they were coordinated to metal cations as monoanionic bidentate in the complexes 3 and 4. There was not any hydrate water in the metal complexes. The complexes of 1 and 2 have four moles of aqua ligand, and the other complexes have two moles. Thermal decomposition of each complex starts with dehydration, and then the decomposition of organic parts goes. The thermal dehydration of the complexes takes place in one (for the compounds of 2, 3, 4) or two (for the compound 1) steps. The decomposition mechanism and the thermal stability of the complexes under investigation were determined on the basis of their structures. Metal oxides were obtained as the final decomposition product. 相似文献