排序方式: 共有206条查询结果,搜索用时 125 毫秒
181.
Mohammad R. Tamadondar Reza Zarghami Maryam Tahmasebpoor Navid Mostoufi 《Particuology》2014,(5):75-83
The dynamic features of an agglomerate bubbling fluidization of nanoparticles were investigated through the analysis of pressure fluctuations. Experiments were carried out in a lab-scale fluidized bed at ambient conditions using 10-15 nm silica nanoparticles without any surface modification. Pressure fluctuation signals were processed in both frequency and time-frequency domains to characterize the behavior of various scales of phenomena (i.e.. macro-, meso-, and micro-structures) during fluidization. Due to the aggregation of nanoparticles, three separate broad peaks were observed in the frequency spectra of the pressure signals measured in the bubbling fluidized bed of nanoparticles. A non-intrusive method based on the decoupling of pressure fluctuations recorded simultaneously in the plenum and in the bed was used to determine the approximate size of the bubbles in the bed. 相似文献
182.
Mohammad Navid Soltani Rad 《Journal of Saudi Chemical Society》2018,22(3):329-336
A simple, mild, highly efficient and transition metal-free protocol for synthesis of ynones in an ionic liquid is described. In this approach, the coupling reaction of different acid chlorides with terminal alkynes was efficiently carried out using 0.05 mol% MgCl2 in the presence of triethylamine in [bmim]Br at room temperature to afford the corresponding ynones in good to excellent yields. This method is highly efficient for various acid chlorides and alkynes including aliphatic, aromatic, and heteroaromatic substrates bearing different functional groups. The influence of some parameters in this reaction including type of ionic liquid, base and catalyst has been discussed. 相似文献
183.
Mohammad Saeid Hosseini Zahra Hashemi-Pour Navid Hosseini 《International journal of environmental analytical chemistry》2016,96(10):945-958
In this study, a new sensitised spectrofluorometric method was presented as a probe sensor for hypochlorite analysis in oral and tap water samples. By capping L-tyrosine (Tyr) on ZnSe nanoparticles, stable quantum dots (QDs) were obtained. In comparison with Tyr, the fluorescence (FL) emission of Tyr-capped ZnSe is enhanced and shifted to greater wavelength, which causes to enhance the sensitivity for the determination of hypochlorite. Based on the FL quenching of the Tyr-capped ZnSe QDs, hypochlorite concentration was detected at buffering pH of 7 in the range of 5.15 × 10?5?2.57 × 10?2 g L?1. Relative standard deviation and detection limit were found to be 0.83% and 2.06 × 10?5 g L?1, respectively. In comparison with the other methods of hypochlorite determination, this method is simple, fast and inexpensive, with low sample volume consumption. It also exhibits a good selectivity. 相似文献
184.
185.
Gazaleh Imani Shakibaei Hamid Reza Khavasi Peiman Mirzaei Ayoob Bazgir 《Journal of heterocyclic chemistry》2008,45(5):1481-1484
186.
Mohammad Navid Soltani Rad Somayeh Behrouz Ali Khalafi-Nezhad 《Tetrahedron letters》2008,49(7):1115-1120
An efficient and selective method for esterification of alcohols using N-(p-toluenesulfonyl)imidazole (TsIm) is described. In this method, alcohols are refluxed with a mixture of RCO2Na (R: alkyl and aryl), TsIm, and triethylamine in the presence of catalytic amounts of tetra-n-butylammonium iodide (TBAI) in DMF to afford the corresponding esters in good yields. This methodology is highly efficient for various structurally diverse alcohols with selectivity for ROH: 1° > 2° > 3°. 相似文献
187.
Azadeh S. Hashemi Doulabi Hamid Mirzadeh Mohammad Imani Shahriar Sharifi Mohammad Atai Shahram Mehdipour‐Ataei 《先进技术聚合物》2008,19(9):1199-1208
Biodegradable polymers have currently attracted high interest as ideal carriers in drug delivery and tissue engineering applications. In situ forming devices based on these materials will synergistically provide the advantages of the customary prefabricated devices as well as ease of administration. To acheive these objectives, optically transparent and biodegradable macromers based on poly(ethylene glycol) and fumaric acid copolymers were synthesized using propylene oxide as a different proton scavenger to enhance in situ photocrosslinking capability. The macromers in different compositions were then photocured for 300 sec in the presence of a visible light initiator/accelerator couple and also a reactive diluent. Characterization of the macromers and the resulting networks were performed using different spectroscopic, chromatographic, physical, and thermal analysis techniques. The resulted shrinkage strain of the macromers upon photocuring was studied using the bounded disk technique, and initial shrinkage strain rates were obtained by numerical differentiation. Our results suggest that the compositions based on these unsaturated aliphatic polyesters are potentially useful to develop injectable, in situ photocrosslinkable carriers for drug and cell delivery applications. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
188.
Afsaneh Feiz Ghazaleh Imani Shakibaei Zahra Yasaei Hamid Reza Khavasi Ayoob Bazgir 《Helvetica chimica acta》2011,94(9):1628-1637
A new four‐component synthesis of spiro[4H‐indeno[1,2‐b]pyridine‐4,3′‐[3H]indoles] and spiro[acenaphthylene‐1(2H),4′‐[4H‐indeno[1,2‐b]pyridines] by the reaction of indane‐1,3‐dione, 1,3‐dicarbonyl compounds, isatins (=1H‐indole‐2,3‐diones) or acenaphthylene‐1,2‐dione, and AcONH4 in refluxing toluene in the presence of a catalytic amount of pyridine is reported. 相似文献
189.
Mohammad Navid SoltaniRad Ali Khalafi‐Nezhad Somayeh Babamohammadi Somayeh Behrouz 《Helvetica chimica acta》2010,93(12):2454-2466
A convenient and efficient method for a one‐pot conversion of N‐alkylisatins to N‐alkylisatin O‐alkyloximes 7a – 7n as potential chemotherapeutic agents is described (Scheme) (isatin=1H‐indole‐2,3‐dione). In this method, the microwave‐assisted three‐component reaction of N‐alkylisatins 8 , hydroxylamine hydrochloride, and diverse alkyl halides in the presence of K2CO3 and Bu4NBr furnishes the corresponding N‐alkylisatin O‐alkyloximes under solvent‐free condition in short times (2–10 min) and good to excellent yields (62–83%). The O‐alkylation of in situ generated isatin oximes with alkyl halides was achieved regioselectively, and (Z)‐O‐alkyloximes were produced dominantly. PM3 Semi‐empirical quantum‐mechanic calculations were performed to rationalize the evidences, and the calculations indicated a lower heat of formation for the (Z)‐O‐alkyloximes. 相似文献
190.
Kumar S Choi WT Dong CZ Madani N Tian S Liu D Wang Y Pesavento J Wang J Fan X Yuan J Fritzsche WR An J Sodroski JG Richman DD Huang Z 《Chemistry & biology》2006,13(1):69-79
Chemokines and their receptors play important roles in numerous physiological and pathological processes. To develop natural chemokines into receptor probes and inhibitors of pathological processes, the lack of chemokine-receptor selectivity must be overcome. Here, we apply chemical synthesis and the concept of modular modifications to generate unnatural synthetically and modularly modified (SMM)-chemokines that have high receptor selectivity and affinity, and reduced toxicity. A proof of the concept was shown by transforming the nonselective viral macrophage inflammatory protein-II into new analogs with enhanced selectivity and potency for CXCR4 or CCR5, two principal coreceptors for human immunodeficiency virus (HIV)-1 entry. These new analogs provided insights into receptor binding and signaling mechanisms and acted as potent HIV-1 inhibitors. These results support the concept of SMM-chemokines for studying and controlling the function of other chemokine receptors. 相似文献