Sharif Digital Repository

7H-benzimidazo[2,1-a]benz[de]isoquinolin-7-one compounds were prepared in a selective manner by reaction between o-phenylenediamines and appropriate 1,8-naphthalenedicarboxylic anhydrides using acidic alumina under microwave irradiation  

Free Content Selective synthesis of conjugated enynes from α-arylalkynols using LiCl-Acidic Al2O3 under solvent-free conditions  

A novel superabsorbent hydrogel composite based on gelatin has been prepared by graft copolymerisation of acrylic acid and acrylamide in the presence of kaolin powder, using methylene-bisacrylamide (MBA) as a crosslinking agent and ammonium persulfate as an initiator. The synthetic variables affecting the water absorbency of the resulting superabsorbent composite were studied and the composite structure was confirmed using FT-IR spectroscopy. A new absorption band at 1728 cm-1 in the composite spectrum confirmed the presence of a kaolin-organic polymer linkage. The effect of kaolin content and MBA concentration showed that increasing these parameters decreased the water absorbency of the... 

γ-Alumina is used to catalyze the Cannizzaro reaction in the absence of any base under microwave irradiation in high yields. In the case of terephthalaldehyde the reaction is carried out with high selectivity  

Conjugated enynes, dienes and simple olefins have been cleanly and selectively synthesized, good-to-excellent yields, by dehydration of corresponding alcohols using focused microwave irradiation on the surface of LiCI-acidic alumina  

This article describes the synthesis and swelling behavior of a superabsorbing hydrogel based on sodium alginate (NaAlg) and polyacrylonitrile (PAN). The physical mixture of NaAlg and PAN was hydrolyzed with a solution of NaOH to yield an alginate-poly(sodium acrylate-co-acrylamide) [Alg-poly(NaAA-co-AAm)] superabsorbent hydrogel. A proposed mechanism for hydrogel formation was suggested, and the structure of the product was established with Fourier transform infrared spectroscopy. The effects of reaction variables were systematically optimized to achieve a hydrogel with a swelling capacity as high as possible. Under the optimized conditions concluded, the maximum capacity of swelling in... 

Arylalkynols were converted into both conjugated enynes and arylacetylenic compounds using p-TsCl/Al2O3 and KOH/Al2O3 respectively in classical heating or microwave irradiation methods in good yields  

Microwave induced Cannizzaro reaction, which was performed in presence of neutral γ-alumina as a polymeric catalyst, was discussed. Cannizzaro reaction was carried out on alumina surface and other unknown products were also obtained. Solvent extraction method was utilized to isolate mild and selective benzyl alcohol and carboxylic acids  

In this work we report a fast two-step microwave activated synthesis of the ZnS:Mn nanocrystals. Zn(NO3)2 and Na2S 2O3 were used as the precursors and Mn(NO 3)2 was employed as the source of the impurity. The aqueous synthesis was based on the heat sensitivity of Na2S 2O3, which releases some S species on heating. Consequently, the reaction was well activated under microwave irradiation resulting in formation of ZnS:Mn nanocrystals. Thioglycerol (TG) was also used as the capping agent and the catalyst of the reaction. The synthesis process was done in two steps, i.e. 1 min irradiation without TG and then injection of TG and continuation of irradiation. ZnS:Mn nanocrystals were quickly formed... 

CdS nanoparticles were synthesized by a thermochemical method by using Na2S2O3 and CdSO4 as the precursors and thioglycerol as the capping agent. We have investigated the effect of different temperatures on the size and crystalline phase of the CdS nanoparticles. The results of the optical spectroscopy and XRD analyses clarified that increasing the synthesis temperature increased the final nanoparticles size and also changed the crystalline phase of the particles from hexagonal to cubic phase. The size of the synthesized particles was less than 4nm. TEOS was also used in cooperation with thioglycerol for better surface passivation. The results of the PL analysis showed that using this... 

Poly(vinyl alcohol) (PVA) is a biocompatible polymer which can be physically crosslinked by Borax to form hydrogel. PVA-Borax (PB) hydrogel is a promising candidate for drug delivery system. Therefore, it is necessary to find the quantitative relationship between drug release rate and network structure of PB hydrogels to predict and control drug release rate. In this work, at first step the optimum ratio of Borax: PVA was determined by studying the interactions between PVA chains and Borax molecules by means of Fourier transform infrared spectroscopy, while viscoelastic properties of prepared PB hydrogels were measured in the oscillatory shear flow field. In the following, curcumin as a... 

Nowadays, environmental hazards caused by plastic wastes are a major concern in academia and industry. Utilization of biodegradable polymers derived from renewable sources for replacing common petroleum-based plastics is a potential solution for reducing the problem. In this regard, starch has become one of the most promising alternatives to non-biodegradable polymers for depleting plastic waste thanks to its low expense, abundance, renewability and biodegradability. However, the main drawbacks of starch are its poor processability, weak mechanical properties and severe hydrophilicity. In this work, thermoplastic starch (TPS) samples have been prepared using glycerol and sorbitol as... 

CdS nanocrystals were prepared through a thermally activated (thermochemical) method. The synthesis was performed in two different oxygen-saturated and Ar purged atmospheres. Na2S2O3 was used as a heat-sensitive source of S in the experiments. Thioglycerol was also applied as the capping agent to restrain the growth. The growth was activated by heating and controlled by solution pH. The results demonstrated a considerably higher luminescence intensity for the synthesis in oxygen-saturated atmosphere. This could show the role of luminescent oxygen trap states created inside the CdS nanocrystals. The improved luminescence was observed for the synthesis at different solution pHs. Nevertheless,... 

CdS nanocrystals were thermochemically (thermally activated) synthesized thorough the reaction between CdSO4 and Na2S 2O3 in an aqueous solution. Thioglycolic Acid (TGA) was used as the capping agent and catalyst of the reaction. The method was based on heat activated dissociation of Na2S2O3 and controllable release of S and free electrons in the solution. CdS NCs were formed by heating the sample solution at 96 C for 1 h. The results of optical spectroscopy and transmission electron microscopy demonstrated round shape NCs with sizes about 3.0 nm. The nanocrystals were also luminescent and represented a broad emission with a peak located at 515 nm and FWHM of 160 nm. Several samples were... 

CdS nanoparticles were grown using CdSO4 and Na 2S2O3 as the precursors and thioglycerol (TG) as the capping agent. TG was shown to exhibit a catalytic role in the reaction and also acted as a capping agent. It was demonstrated that size growth is linearly related to the temperature of the reaction, i.e.the sizes can be controllably adjusted by temperature. The crystalline phase of the nanocrystals was also dependent on the temperature of growth: higher temperature favours the cubic phase. The pH also plays an important role in nanoparticle growth, as lower pH leads to a higher release rate of sulfur species. At pH as high as 10, the growth rate remains slow even at boiling temperature. This... 

A polypropylene (PP) sheet was successfully applied as an extracting medium for trace enrichment of fluoxetine (FLX) from urine samples, followed by high performance liquid chromatography-fluorescence detection (HPLC-FD). The extraction medium was a square, 1 × 1 cm2 piece of polypropylene membrane sheet that was conditioned in methanol. The extraction process was conveniently carried out using a 5 mL urine sample. After extraction, the PP sheet was withdrawn and transferred to a glass vial for performing the desorption process using 210 μL organic solvent. After complete drying, the residue was dissolved in 50 μL of methanol and an aliquot of 20 μL was, finally, injected into the HPLC... 

In this article, a new method is proposed to identify the constants of the extended Drucker-Prager yield surface for polypropylene nanocomposites. The method is based on optimizing the difference between the numerical and the experimental results of a three-point bending test. The test specimens are made of polypropylene/nanoclay and polypropylene/nano-calcium carbonate nanocomposites with different nanoparticles content. Moreover, the effect of composite filler content on the extended Drucker-Prager constants of polypropylene, as the composite matrix, is investigated. Inasmuch as numerical simulation is usually very time-consuming and highly nonlinear, a surrogate-based model with radial... 

A simple, rapid tandem mass spectrometric method for recognition of chiral molecules by proton transfer reactions with chiral sec-butylamines and sec-butanols is reported  

Recently, the use of biodegradable polymers became the applicable solution to reduce the environmental concerns, which are created by plastic wastes as well as restrictions of petroleum-based synthetic polymers. By this point of view, polylactic acid (PLA) as a biodegradable and bio-based polymer is resolving both aforementioned issues. While, the high cost of PLA and its slow biodegradation rate make researchers to blend it with a faster one, for instance, thermoplastic starch (TPS). Adding TPS into PLA can influence on the morphological structure, thermal stability, and biodegradability. In this study, the well-tuned co-plasticized TPS via sorbitol/glycerol mixture was melt mixed with PLA... 

Polyhedral oligomeric silsesquioxanes are 3D nanoscaled materials with large potential in solid phase microextraction (SPME). Here, as a case study, an octaglycidyldimethylsilyl modified polyhedral oligomeric silsesquioxane network is described. It was deposited on a stainless steel wire via a sol–gel method and used as a fiber coating for SPME of aromatic compounds. The uniform pore structure, high surface area, and hydrophobicity of the network make it susceptible toward isolation of non-polar and semi-polar chemical compounds. The performance of the fiber coating was tested with three classes of environmental pollutants, viz. chlorobenzenes (CBs), benzenes (benzene, toluene, ethylbenzene,...