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161.
Dihydropyrimidinone derivatives were prepared by tri-component reaction of ethyl aceto acetate, aldehydes and thiourea in the presence of modified montmorillonite nanostructure as a catalyst and used as key intermediates for the synthesis of ethyl-5-(aryl)-2-(2-alkokxy-2-oxoethylidene)-7-methyl-3-oxo-3,5-dihydro-2H-thiazolo[3,2-a]pyri midine-6-carboxylate derivatives with use of diethyl and dimethyl acetylene dicarboxylate by two methods: (a) in methanol as a solvent under ultrasonic irradiation at ambient temperature (b) in methanol as a solvent at ambient temperature (conventional magnetic stirring). Ultrasound-assisted synthesis provides excellent yields in short reaction times (15–25 min) at room temperature. 相似文献
162.
Nihat Ali IsitmanCevdet Kaynak 《Polymer Degradation and Stability》2011,96(12):2284-2289
This study describes the mechanism of flammability reduction in flame-retarded polymer matrix organo-montmorillonite reinforced nanocomposites. Morphologies of untested polymer nanocomposites and char residues formed by combustion in the mass loss calorimeter are characterized by XRD and TEM techniques. It is postulated that a combination of well-dispersed montmorillonite platelets and flame retardants in the polymer matrix provides nano-structured char formation. Initial montmorillonite dispersion in flame-retarded nanocomposites is found to be a major controlling factor on formed char nanostructures. An initially intercalated structure is invariantly converted to complete montmorillonite collapse whereas an initially exfoliated structure transforms to nano-structured chars demonstrating retained exfoliation or a new state of intercalation via incomplete collapse of montmorillonite layers. It is proposed that nano-structured char formation is the effective mechanism of flammability reduction, i.e. reduction in rate of heat release during combustion, in flame-retarded polymer nanocomposites. 相似文献
163.
Ameen Ali Abu-Hashem 《Journal of heterocyclic chemistry》2021,58(1):74-92
4-oxo-4-phenylbutanehydrazide 3 was reacted with aryl or alkyl isothiocyanates to give the corresponding N-substituted-2-(4-oxo-4-phenylbutanoyl) hydrazine-1-carbothioamide 4a-c . Cyclization of thiosemicarbazides 4a-c with sodium hydroxide led to the formation of 3-(4-sub-5-thioxo-1,2,4-triazol-3-yl)-propanone 5a-c . Desulfurization of thiosemicarbazides 4a-c by mercuric oxide afforded 3-(5-(sub-amino)-1,3,4-oxadiazol-2-yl)-propanone 6a-c . The reaction of 4a-c with phosphorus oxychloride gave 3-(5-(sub-amino)-1,3,4-thiadiazol-2-yl)-propanone 7a-c . Treatment of 4a-c with ethyl-bromoacetate or α-bromopropionic acid gave N′-(3-sub-thiazolidin-2-ylidene)-butanehydrazide 8a-c and (N′-(3-sub-oxothiazolidin-2-ylidene)-butanehydrazide 9a-c . Chlorination of oxothiazolidine-hydrazide 9a-c by phosphorus oxychloride afforded N-(3-sub-4-oxothiazolidine)-butane-hydrazonoyl-chloride 10a-c . The reaction of 10a-c with mercaptoacetyl-chloride yielded 2-((4-benzoyl-thiopyrane) hydrazono)-3-sub-thiazolidinone 11a-c . Also, reacted of 10a-c with hydrazine hydrate afforded N″-(3-sub-oxothiazolidine)-butane-hydrazon-hydrazide 12a-c . The 3-sub-2-((pyridazine) hydrazono) thiazolidinone 13a-c was obtained by cyclization of 12a-c via refluxing in DMF. The reaction and cyclized of 9a-c with chloroacetyl-chloride in ethanolic KOH afforded 1-((3-sub-4-oxothiazolidine) amino)-azepine-dione 14a-c . The chemical structures of the new compounds have been confirmed by diverse spectroscopy analyses such as IR, NMR, MS, and elemental analysis. The synthesized compounds were tested for their antimicrobial activity and these compounds were considered (Pyridazin-hydrazono-thiazolidinone 13a-c , oxothiazolidin-azepinedione 14a-c , N-thiazolidin-hydrazon-hydrazide 12a-c , and thiopyran-hydrazono-thiazolidinone 11a-c ) the most effective as antimicrobial activity. 相似文献
164.
[reaction: see text] Pyridinium hydrobromide perbromide (Py x HBr3) catalyzes effectively the aziridination of electron-deficient as well as electron-rich olefins using Chloramine-T (N-chloro-N-sodio-p-toluenesulfonamide) as a nitrogen source to afford the corresponding aziridines in moderate to good yields. 相似文献
165.
A new low-cost pH sensor developed by immobilizing a direct indicator dye to porous and transparent acetylcellulose film. This sensor was fabricated by binding α-Naphthyl Red and Alizarine Yellow GG to a cellulose acetate film that had previously been subjected to an exhaustive base hydrolysis. The membranes have good durability (>12 months) and a short response time (<5 s). The method is easy to perform and uses acetylcellulose as a carrier. The reagents used for the activity of the cellulose support are inexpensive, nontoxic, and widely available. The Alizarine Yellow GG sensor can be used for direct determination of pH in alkaline media without any alkaline error. 相似文献
166.
Closed form one centre partial wave perturbation results are obtained through second order in the energy for H-like molecules with arbitrary nuclear charges. The expansion centre for the method is taken at an arbitrary point along the internuclear axis and the zeroth-order wave function is a screened “1s” function centred at the expansion point. Various fixed one centre calculations of other workers for the lsσ states of H and HeH++ and for the 2pσ state of HeH++ are generated as limiting cases of this more general treatment. The floating one centre perturbation results for the 1sσ states of H2+ and HeH++ are used as models for discussing the usefulness of allowing the expansion centre in the one centre method to be a function of nuclear configuration. 相似文献
167.
Summary Palladium and uranium react with 4,4-acetalidine-bis-(3-methyl isoxazolone-5) in acid medium to give yellow color having a visual limit of identification at 2 and 15g per ml. This color reaction provides the basis of a new method for colorimetric determination of palladium and uranium. Copper also gives yellow color but it cannot be determined with this color reaction because the color intensity is not stable. The maximum tolerable limit of various ions is reported.
Zusammenfassung Pd und U reagieren in saurem Milieu mit 4,4-Acetalidin-bis-(3-methyl-isoxazolon-5) unter Gelbfärbung mit einer Erfassungsgrenze von 2 bzw. 15g/ml. Diese Farbreaktion dient als Grundlage für eine neue kolorimetrische Methode für Pd und U. Cu gibt zwar auch eine Gelbfärbung, kann aber damit nicht bestimmt werden, da die Farbintensität nicht beständig ist. Die maximal tolerierbare Menge der Fremdionen wird angegeben.相似文献
168.
Ali Deeb Mahmoud Kotb Mohamed El-Abbasy 《Phosphorus, sulfur, and silicon and the related elements》2013,188(11):2245-2252
3-Substituted pyrimido[4′,5′:4,5]thieno[2,3-c]pyridazine-2,4-di-ones and 3-amino-2-methylpyrimido[4′,5′:4,5]thieno[2,3-c]pyridazine-4-ones were synthesized starting from ethyl 5-aminothieno[2,3-c] pyridazine-6-carboxylate 1. Reaction of amino ester 1with phenyl isothiocyanate affords thiourea derivative 10which undergo further transformation to the related fused heterocyclic systems. 相似文献
169.
Ayhan S. Demir Nurettin Camkerten Hulya Akgun Cihangir Tanyeli Ali S. Mahasneh David S. Watt 《合成通讯》2013,43(15):2279-2289
The α-oxidation of aryl alkyl ketones using manganese(III) acetate in the presence of various carboxylic acids and (1S)-(+)-10-camphorsulfonic acid provided a convenient synthesis of α-acyloxy, α-(10-camphorsulfonyloxy), and α-hydroxy derivatives in good yield. 相似文献
170.
Yoon-Kyoung Cho Ali Dhinojwala Steve Granick 《Journal of Polymer Science.Polymer Physics》1997,35(17):2961-2968
We study the drainage of a near-theta solvent through densely grafted polymer layers and compare to recent notions that these layers display little permeability to solvent flow at surface separations less than a “hydrodynamic thickness.” The solvent is trans-decalin (a near-theta solvent at the experimental temperature of 24°C). The polymer is polystyrene (PS) end-attached to two opposed mica surfaces via the selective adsorption of the polyvinylpyridine (PVP) block of a PS-PVP diblock copolymer. The experimental probe was a surface forces apparatus modified to apply small-amplitude oscillatory displacements in the normal direction. Out-of-phase responses reflected viscous flow of solvent alone—the PS chains did not appear to contribute to dissipation over the oscillation frequencies studied. The value of the hydrodynamic thickness (RH) was less than the coil thickness (Lo) measured independently from the onset of surface–surface interactions in the force-distance profile, implying significant penetration of the velocity field into the polymer layer. As the surface–surface separation was reduced from 3Lo to 0.3Lo, the apparent hydrodynamic thickness (R) decreased monotonically to values R ≪ RH. Physically, this indicates that the “slip plane” moved progressively closer to the solid surfaces with decreasing surface–surface separation. This was accompanied by augmentation of the effective viscosity by a factor of up to approximately 5, indicating somewhat diminished permeability of solvent through the overlapping polymer layers. Similar results hold for the flow through surface-anchored polymers in a good solvent. It is interesting to note the strong stretching of densely end-grafted polymers in a theta solvent. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2961–2968, 1997 相似文献