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1.
The conversion of 3-methyl-4-benzyl-4-chloro-2-pyrazolin-5-one 10b was catalyzed by a mixture of potassium fluoride and alumina to give syn-(methyl, benzyl)bimane 6 (62%) without detectable formation of the anti isomer, A6 [a 1 : 1 mixture (87%) of the isomers 6 and A6 was obtained when the catalyst was potassium carbonate]. In a similar reaction syn-(methyl,carboethoxymethyl)bimane 7 (15%) with the anti isomer A7 (36%) was obtained from 3-methyl-4-carboethoxymethyl-4-chloro-2-pyrazolin-5-one 10c . syn-(Methyl, β-acetoxyethyl)bimane 8 (70%) was obtained from 3-methyl-4-β-acetoxyethyl-4-chloro-2-pyrazolin-5-one 10d (potassium carbonate catalysis) and was converted by hydrolysis to syn-(methyl, β-hydroxyethyl)bimane 9 (40%). Acetyl nitrate (nitric acid in acetic anhydride) converted anti-(amino,hydrogen)bimane 11 to anti-(amino,nitro)bimane 15 (91%), anti-(methyl,hydrogen)bimane 13 to anti-(methyl,nitro)(methyl,hydrogen)bimane 16 (57%), and degraded syn-(methyl,hydrogen)bimane 12 to an intractable mixture. Treatment with trimethyl phosphite converted syn-(bromomethyl,methyl)bimane 17 to syn-(dimethoxyphosphinylmethyl,methyl)bimane 18 (78%) that was further converted to syn-(styryl,methyl)bimane 19 (29%) in a condensation reaction with benzaldehyde. Treatment with acryloyl chloride converted syn-(hydroxymethyl,methyl)bimane 20 to its acrylate ester 21 (22%). Stoichiometric bromination of syn-(methyl,methyl)bimane 1 gave a monobromo derivative that was converted in situ by treatment with potassium acetate to syn-(acetoxymethyl,methyl)(methyl,methyl)bimane 47 . N-Amino-μ-amino-syn-(methylene,methyl)bimane 24 (68%) was obtained from a reaction between the dibromide 17 and hydrazine. Derivatives of the hydrazine 24 included a perchlorate salt and a hydrazone 25 derived from acetone. Dehydrogenation of syn-(tetramethylene)bimane 26 by treatment with dichlorodicyanobenzoquinone (DDQ) gave syn-(benzo,tetramethylene)bimane 27 (58%) and syn-(benzo)bimane 28 (29%). Bromination of the bimane 26 gave a dibromide 29 (92%) that was also converted by treatment with DDQ to syn-(benzo)bimane 28 . Treatment with palladium (10%) on charcoal dehydrogenated 5, 6, 10, 11-tetrahydro-7H,9H-benz [6, 7] indazol [1, 2a]benz[g]indazol-7,9-dione 35 to syn-(α-naphtho)bimane 36 (71%). The bimane 35 was prepared from 1,2,3,4-tetrahydro-1-oxo-2-naphthoate 37 by stepwise treatment with hydrazine to give 1,2,4,5-tetrahydro-3H-benz[g]indazol-3-one 38 , followed by chlorine to give 3a-chloro-2,3a,4,5-tetrahydro-3H-benz[g]indazol-3-one 39 , and base. Dehydrogenation over palladium converted the indazolone 34 to 1H-benz[g] indazol-3-ol 36 . Helicity for the hexacyclic syn-(α-naphtho)bimane 36 was confirmed by an analysis based on molecular modeling. The relative efficiencies (RE) for laser activity in the spectral region 500–530 nm were obtained for 37 syn-bimanes by reference to coumarin 30 (RE 100): RE > 80 for syn-bimanes 3, 5, 18 , and μ-(dicarbomethoxy)methylene-syn-(methylene,methyl)bimane 22 : RE 20–80: for syn-bimanes 1,2,4,20,24,26 , and μ-thia-syn-(methylene,methyl)bimane 50 : and RE 0-20 for 26 syn-bimanes. The bimane dyes tended to be more photostable and more water-soluble than coumarin 30. The diphosphonate 18 in dioxane showed laser activity at 438 nm and in water at 514 nm. Presumably helicity, that was demonstrated by molecular modeling, brought about a low fluorescence intensity for syn-(α-naphtho)bimane 36 , Φ0.1, considerably lower than obtained for syn-(benzo)bimane 28 , Φ0.9.  相似文献   
2.
The present work details optimization of a stable acid chloride bath for electroplating of bright Zn-Co alloy on mild steel using gelatin and glycine as additives. It was found that the addition of gelatin along with glycine changed the deposition pattern markedly. A suitable bath has been formulated using conventional Hull cell experiments. The bath under plating conditions were found to exhibit anomalous codeposition with preferential deposition of less noble (zinc) over more noble (cobalt) as characterized by Zn-Fe group metal alloys. Investigation revealed that the current density (c.d.), temperature, and pH of the bath have strong effect on the composition of the deposit. Influence of bath constituents and operating parameters on appearance and composition of deposits were studied as measure of their performance against corrosion. A variety of deposits were obtained and their corrosion resistances were measured by Tafel method with/without chrome passivation. Experimental results demonstrated the fact that the corrosion resistances of Zn-Co alloys increased with percent of Co in the deposit except at very high c.d. This is due to the fact at very high c.d. the deposit becomes very porous and thick as evidenced by SEM image. The formation of Zn-Co alloy is confirmed by EDAX analysis. A stable chloride bath for Zn-Co alloy deposition has been proposed and discussed. The formation of passive film on chromatization is indicated by almost same E corr value of all Zn-Co electroplates irrespective of the current densities at which they have been deposited. Published in Russian in Elektrokhimiya, 2009, Vol. 45, No. 7, pp. 811–816. The text is published in the original.  相似文献   
3.
Silk from the domesticated silk worm Bombyx mori procures foreign body response naturally, so it has been utilized as a biomaterial for decades. In India the prime focus of the sericulture industry is to improve silk production with high quality silk. Naturally, the silk worm builds its cocoon not only with silk proteins, but also with antimicrobial proteins to avoid infection since the cocoon is non-motile and non-feeding. The aim of the present study is to elucidate the antimicrobial proteins that persist in the cocoon of the silk worm Bombyx mori. At the pupal stage, the silk worm cocoon shell extract was prepared from the day of pupation (P0) to the day of natural rupture of the cocoon for the eclosion of moth (NR). Using the cocoon shell extract a microbial susceptibility test was performed by the disc diffusion method against the microbes Escherchia coli, Bacillus cereus, Staphylococcus aureus, Pseudomonas aeruginosa, and Klebsiella pneumoniae. The development of a zone of inhibition against the microbes confirmed the presence of antimicrobial/immunogenic activity of the cocoon shell extract. For further analysis, the cocoon shell extract was subjected to 7-15% sodium dodecyl sulfate/polyacrylamide gel electrophoresis (SDS-PAGE). The protein profile of the cocoon extract revealed the coomassie blue stained bands resolved from the 150-15 kDa molecular range. Interestingly, a polypeptide localized at around 29 kDa showed remarkable expressional changes during the development of pupa. To characterize the 29 kDa protein, it was eluted from the gel, digested with trypsin and analyzed by matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS). The trypsin-digested peptide peaks were analyzed through MASCOT and peptides were matched with the NCBI nr database. The peptides were very well matched with the 18 wheeler protein, which is reported to be responsible for innate immunity, belonging to the Toll family in insects and responsible for cellular mediated immunity.  相似文献   
4.
The variation of DC electrical conductivity and the optical properties of thermally evaporated a- (Sb2Se3)100−xSnx thin films with temperature have been studied. It is found that the thermal activation energy decreases, while the optical gap first increases (up to x=1) and then decreases, with the increase in Sn content. These results have been explained by taking into consideration the structural modifications induced by the incorporation of Sn into the parent alloy. The variation in the conductivity prefactor (σo) with Sn addition indicates a change in the dominant conduction transport mechanism from extended states to localized states. An experimental correlation between the activation energy and the pre-exponential factor has been observed, indicating the validity of Meyer–Neldel rule in the studied samples.  相似文献   
5.
In this article, we discuss a number of storage models of finite capacity with random inputs, random outputs, and linear release policy. They form a class of one-dimensional master equations with separable kernels. For this class of problems, the integral equations for first overflow or first emptiness can be transformed exactly into ordinary differential equations. Analysis is done with separable kernel. For all the stochastic models, two barriers are considered: one at X = 0 and the other at X = k, and the barriers are treated as absorbing or reflecting. The imbedding method is used to derive a third order differential equation. We consider first passage times for overflow without or with emptiness of the dam. We also study the passage times for first emptiness with and without overflows. The expected amount of overflows in a given time is also calculated. Finally, by suitable statistical features, all these models are converted into diffusion process with drift. Closed form solutions are obtained for all the problems in terms of Laplace transform functions. For the diffusion process with drift first passage time density is arrived at by treating X = 0 and X = k as absorbing barriers. One of the barriers as reflecting is also studied.  相似文献   
6.
7.
In this article, we discuss finite dam models to study the expected amount of overflow in a given time. The inputs into the dam are taken as random and there are two types of outputs—one is random and the other is deterministic which is proportional to the content of the dam. The master equation for the expected amount of overflow is an one dimensional equation with separable kernel. For this class of master equation, the integral equation for the expected amount of overflow has been transformed exactly into ordinary differential equation with variable coefficients. The imbedding method is used to study the expected amount of overflow in a given time without emptiness in this period. We also consider the model for the expected amount of overflow in a given time with any number of emptiness of the dam in this period. The results are derived in the form of a third order differential Equation for the Laplace transformation function for the expected overflow. The closed form analytical solutions are obtained in terms of beta functions and degenerate hyper-geometric functions of two variables.  相似文献   
8.
A series of fused quinolinyl and quinolonyl pyrans were synthesized via a one‐pot reaction of quinolinyl and quinolonyl carbaldehydes, malononitrile, and a 1,3‐diketone. The reactions were catalyzed by a new humic acid supported 1‐butyl‐3‐methyl imidazolium thiocyanate ionic liquid under microwave irradiation conditions. Antimicrobial, antioxidant, and toxicity studies displayed various biological activities depending on structure of the pyrans.  相似文献   
9.
The effect of thermal annealing on the electrical and optical properties of a thin film of Se-Te-Bi alloy has been studied. It has been found that the mechanism of optical absorption follows a non-direct transition. The optical band-gap decreases with an increase in the Bismuth concentration. The electrical conductivity of the as-deposited and annealed films has been found to be of Arrhenius type. The results are discussed on the basis of rearrangements of defects and disorders in the chalcogenide systems. PACS 71.23.An; 73.61.-r; 73.61Jc; 74.25Gz; 78.66Jg  相似文献   
10.
A one‐pot, multicomponent, convergent microwave synthesis of some new pyranyl‐ and chromenyl‐substituted quinolines has been reported. Twenty compounds were prepared by the reaction of 2‐methoxy‐3‐formyl quinoline ( 1a‐d ), malononitrile ( 2 ), and kojic acid ( 4a‐d )/1,3‐cyclohexadione or dimedone ( 6a ‐ h )/α‐ or β‐naphthol ( 8a ‐ d , 8e ‐ h ). The structures were confirmed by infrared (IR), 1H nuclear magnetic resonance (NMR), 13C NMR, mass, and single‐crystal X‐ray analyses. On comparison with the use of conventional Lewis acid catalysts and various metal triflates under microwave conditions, the latter contributed to good yields, in specific use of the recyclable Yb(OTf)3 catalyst attributed to high yields of the desired product. The protocol reported herein is solvent free, cost effective, and eco‐friendly.  相似文献   
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