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31.
5-Nitro-2-hydroxy benzaldoxime (I), 3-nitro-4-hydroxy benzaldoxime (II), 3,5-dinitro-2-hydroxy benzaldoxime (III), and 3,5-dinitro-4-hydroxy benzaldoxime (IV) were prepared from their respective nitrated aldehydes. Prepared oximes were characterized by IR spectroscopy, elemental analysis, and mass spectrometry. Suitable crystals of compounds II and III were obtained and molecular structures were determined by means of the single crystal XRD method. All benzaldoximes were investigated by TG. At temperatures above 140 °C, it was observed that compounds II and IV lost one H2O and was converted to the respective benzonitriles. Only thermal analysis peaks of 3,5-dinitro-4-hydroxy benzonitrile (V) were found proper for both experimental and theoretic calculations; whereas, compounds I and III were converted to phenoxazines by Beckmann rearrangement along with dehydration. Beckmann product of compound III is referred as compound VI and its tautomer as compound VII. Similarly only 3,5-dinitro phenoxazine (VIII) was investigated experimentally and theoretically since its thermal analysis peaks were proper for the purpose. DFT-based structure optimizations and frequency analyses were performed at the B3LYP/cc-pVDZ level of theory. The enthalpies of formation for compounds IIIVIII were calculated by means of the complete basis set (CBS-4M) method of Petersson and coworkers to obtain accurate energies. The enthalpies of decomposition for compounds III and IV were obtained from calculated enthalpies of formation according to Hess’ law and were compared with the experimental values which were available from DSC analyses and were found to be in good agreement with the theoretic values.  相似文献   
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A series of thermosensitive hydrogels were prepared from N-[3-(dimethylamino)propyl]methacrylamide (DMAPMA) monomer by using 11.6–17.8% (m/m) N,N-methylenebis(acrylamide) (MBAAm) as the crosslinker and comonomer in water. A kinetic study of the absorption determined the transport mechanism. The diffusion coefficients of these hydrogels were calculated for the Fickian mechanism. It was shown that the swelling behavior of the P(DMAPMA-co-MBAAm) hydrogels can be controlled by changing the amount of MBAAm. The swelling equilibrium of the P(DMAPMA-co-MBAAm) hydrogels was also investigated as a function of temperature in aqueous solutions of the anionic surfactant sodium dodecyl sulfate (SDS) and the cationic surfactant dodecyltrimethylammonium bromide (DTAB). In pure water, irrespective of the amount of MBAAm, the P(DMAPMA-co-MBAAm) hydrogels showed a discontinuous phase transition between 30 and 40 °C. However, the transition changed from discontinuous to continuous with the addition of surfactants, this is ascribed to the conversion of non-ionic P(DMAPMA-co-MBAAm) hydrogel into polyelectrolyte hydrogels due to binding of surfactants through the hydrophobic interaction. Additionally, the amount of free SDS and DTAB ions was measured at different temperatures by a conductometric method, it was found that the electric conductivity of the P(DMAPMA-co-MBAAm) – surfactant systems depended strongly on both the type and concentration of surfactant solutions.  相似文献   
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Nine CuII complexes ( I – IX ) containing the azide ion and bis‐2,6‐(pyrazol‐1‐yl)pyridine (pp), bis‐2,6‐(pyrazol‐1‐yl)pyridine (dmpp), and 2‐(pyrazol‐1‐yl)‐6‐(3,5‐dimethylpyrazol‐1‐yl)pyridine (mpp), which are derivatives of pyrazolylpyridine, were prepared in nonaqueous medium. These complexes were characterized by elemental analyses and IR spectroscopy. Crystals of one of these complexes [CumppClN3 ( VII )] were prepared in suitable size, and a molecular structure of this complex was obtained with X‐ray diffraction method. Complexes were examined by thermogravimetry and differential scanning calorimetry methods. Thermal decomposition was observed in complexes including two azide groups similar to that seen in explosives. In the complexes containing one azide group, formation of the CuI complexes was observed after thermal decomposition of the azide group.  相似文献   
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A new Au(III)-imprinted hydrogel (Au(III)-Imp) was prepared by the photopolymerisation of 4-acryloylmorpholine (AcM), 2-hydroxyethyl acrylate (HEA), and poly(ethylene glycol) diacrylate (cross-linking monomer, PEG-DA) in the presence of gold ions. In addition, non-imprinted hydrogel (N-Imp) was similarly prepared without Au(III) ions The Au(III)-Imp hydrogel was characterised by several techniques. To achieve the optimal conditions, effect of pH, time, and initial metal ion concentrations were investigated using a batch system. The pre-concentration factor for Au(III) ions was found to be at least 100. The analytical parameters of the method were determined and the method was also successfully applied to computer circuit board scrap samples. The reusability of the Au(III)-Imp hydrogel was also determined.  相似文献   
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In the present work, we dealt with exact solutions and conservation laws of the Benjamin-Ono equation. We obtained exact solutions of given equation via the exp$(-\Phi (\xi ))$ method. The obtained solutions are included the hyperbolic functions, trigonometric functions and rational functions. By using the multiplier approach, the conservation laws of the mentioned equation was founded.  相似文献   
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This work aimed to evaluate the phenolic content and in vitro antioxidant, antimicrobial and enzyme inhibitory activities of the methanol extracts and their fractions of two edible halophytic Limonium species, L. effusum (LE) and L. sinuatum (LS). The total phenolic content resulted about two-fold higher in the ethyl acetate fraction of LE (522.82 ± 5.67 mg GAE/g extract) than in that of LS (274.87 ± 1.87 mg GAE/g extract). LC-MS/MS analysis indicated that tannic acid was the most abundant phenolic acid in both species (71,439.56 ± 3643.3 µg/g extract in LE and 105,453.5 ± 5328.1 µg/g extract in LS), whereas hyperoside was the most abundant flavonoid (14,006.90 ± 686.1 µg/g extract in LE and 1708.51 ± 83.6 µg/g extract in LS). The antioxidant capacity was evaluated by DPPH and TAC assays, and the stronger antioxidant activity in ethyl acetate fractions was highlighted. Both species were more active against Gram-positive bacteria than Gram negatives and showed considerable growth inhibitions against tested fungi. Interestingly, selective acetylcholinesterase (AChE) activity was observed with LE and LS. Particularly, the water fraction of LS strongly inhibited AChE (IC50 = 0.199 ± 0.009 µg/mL). The ethyl acetate fractions of LE and LS, as well as the n-hexane fraction of LE, exhibited significant antityrosinase activity (IC50 = 245.56 ± 3.6, 295.18 ± 10.57 and 148.27 ± 3.33 µg/mL, respectively). The ethyl acetate fraction and methanol extract of LS also significantly inhibited pancreatic lipase (IC50 = 83.76 ± 4.19 and 162.2 ± 7.29 µg/mL, respectively). Taken together, these findings warrant further investigations to assess the potential of LE and LS as a bioactive source that can be exploited in pharmaceutical, cosmetics and food industries.  相似文献   
40.
Oxidative stress may produce high level of reactive oxygen species (ROS) following cell exposure to endogenous and exogenous factors. Recent experiments implicate oxidative stress as playing an essential role in cytotoxicity of many materials. The aim of this study was to measure intracellular malondialdehyde (MDA), advanced oxidation protein product (AOPP) levels, and superoxide dismutase (SOD) activities of L929 fibroblasts cultured on PDLLA, polyethylene glycol (PEG), or ethylenediamine (EDA) grafted PDLLA by plasma polymerization method. Cell proliferation on these scaffolds was studied by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay. The study showed that MDA, AOPP levels, and SOD activities in L929 fibroblast cells cultured on all scaffolds were significantly different compared to the control group and each other. The highest MDA (0.42 ± 0.76 nmol/mg protein), AOPP (14.99 ± 4.67 nmol/mg protein) levels, and SOD activities (7.49 ± 3.74 U/mg protein) were observed in cells cultured on non-modified scaffolds; meanwhile, the most cell proliferation was obtained in EDA-modified scaffolds (MDA 0.15 ± 0.14 nmol/mg protein, AOPP 13.12 ± 3.86 nmol/mg protein, SOD 4.82 ± 2.64 U/mg protein). According to our finding, EDA- or PEG-modified scaffolds are potentially useful as suitable biomaterials in tissue engineering.  相似文献   
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