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21.
Twelve different samples of gel spheres were prepared from the biopolymers chitosan, alginate, and gelatin via polyion complex formation in aqueous solution with crosslinking by glutaraldehyde. Dropwise addition of a chitosan/gelatin solution into a solution containing alginate and glutaraldehyde gave the gel spheres. The effects of different ratios of glutaraldehyde (0.25%, 0.50%, 1.0%, and 2.0%), and gelatin (2.5%, 5.0%, and 10.0%) on the characteristics of the gel spheres were evaluated. An increase in the concentration of the glutaraldehyde led to forming true spheres in rigid form. By scanning electron microscopy (SEM), the gel spheres showed fibrous network propagation along the gel membrane surface. Fourier transform infrared (FT-IR) spectroscopy confirmed the crosslinking of the amino groups by the glutaraldehyde and the presence of crosslinking bonds between the amino groups of chitosan and the carboxyl groups in the alginate molecule. Swelling studies showed that increasing the degree of crosslinking increased the density of the polymer network, which led to a decrease in the degree of swelling. The characteristics of the gel spheres will be useful for immobilization and prolonged release of biologically active substances.  相似文献   
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Capmatinib, a recently approved tyrosine kinase inhibitor, is used for the treatment of non-small cell lung cancer. We describe two new HPLC methods for capmatinib quantification in vivo and in vitro. HPLC with a fluorescence detection method was used to quantify capmatinib in plasma for the first time. The method was successfully applied in a pharmacokinetic study following a 10 mg/kg oral dose of capmatinib given to rats. The chromatographic separation was performed using a Eurospher II 100-3 C18H (50 × 4 mm, 3 µm) column and a mobile phase containing 10 mM of ammonium acetate buffer (pH 5.5): acetonitrile (70:30, v/v), at a flow rate of 2.0 mL min−1. The study also describes the use of HPLC-PDA for the first time for the determination of capmatinib in human liver microsomes and describes its application to study its metabolic stability in vitro. Our results were in agreement with those reported using LC-MS/MS, demonstrating the reliability of the method. The study utilized a Gemini-NX C18 column and a mobile phase containing methanol: 20 mM ammonium formate buffer pH 3.5 (53:47, v/v), delivered at a flow rate of 1.1 mL min−1. These methods are suitable for supporting pharmacokinetic studies, particularly in bioanalytical labs lacking LC-MS/MS capabilities.  相似文献   
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Scanning electron microscopy (SEM), X- ray diffraction (XRD), density (d), oxygen molar volume (Vm) and dc conductivity of different compositions of calcium vanadate glasses are reported. SEM exhibits a surface without any presence of a microstructure which is a characteristic of the amorphous phase. The overall features of these XRD curves confirm the amorphous nature of the present glasses. Density was observed to decrease with an increase in V2O5 content. The experimental results were analyzed with reference to theoretical models existing in the literature. It has been observed that the high-temperature conductivity data are consistent with Mott's nearest-neighbor hopping model. However, both Mott variable-range hopping (VRH) and Greaves intermediate range hopping models are found to be applicable. The hopping at high temperatures in the calcium vanadate glasses occurs by non-adiabatic process in contrast to the vanadate glasses formed with conventional network formers. The hopping model of Schnakenberg can predict the temperature dependence of the conductivity data. The percolation model of Triberis and Friedman applied to the small polaron hopping (SPH) regime is also consistent with data. The various model parameters such as density of states, hopping energy, etc., obtained from the best fits were found to be consistent with the glass compositions.  相似文献   
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The condensation of 1,3-bis-silyl enol ethers with benzopyrylium triflates, generated in situ by the reaction of chromones with Me3SiOTf, afforded functionalized 2,3-dihydrobenzopyrans; treatment of the latter with NEt3 or BBr3 resulted in a domino retro-Michael-aldol-lactonization reaction and the formation of a variety of 7-hydroxy-6H-benzo[c]chromen-6-ones. The hydroxy group was functionalized by using Suzuki cross-coupling reactions. The methodology reported was applied to the synthesis of the natural product autumnariol and a new fluorescence dye, which exhibits promising optical properties. 2,3-Dihydro-1H-4,6-dioxachrysen-5-ones were prepared by condensation of chromones with 1,3-bis-silyl enol ethers containing a remote chloride group, domino retro-Michael-aldol-lactonization, and an intramolecular Williamson reaction.  相似文献   
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Journal of Thermal Analysis and Calorimetry - Natural convective flows of Prabhakar-like fractional viscoelastic fluids over an infinite vertical heated wall are studied by introducing the...  相似文献   
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Journal of Thermal Analysis and Calorimetry - During the production of iron(iii) oxide and silver nanoparticles where water is inevitable, little is known on the transport phenomenon in a...  相似文献   
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A series of hyperbranched polyesters was produced by the condensation of the monomer 3,5‐dihydroxybenzoic acid with 1,3,5‐tris(2‐hydroxyethyl) cyanuric acid as a trifunctional central core. The monomer‐to‐core ratio was varied between 3 and 45. The resulting polymers were phenolic‐terminated polyesters. The degree of branching of the polyesters was calculated according to the method described by Fréchet and was found to be in the range of 0.7–0.8. The number‐average molecular weights calculated via 1H NMR spectroscopic degree‐of‐polymerization values are in reasonable agreement with the predicted values derived from the monomer‐to‐core ratio for all prepared polyesters. Thermal and photophysical properties were also studied. Glass‐transition temperatures were determined by differential scanning calorimetry and were found to be relatively independent of the theoretical molar mass. The polyesters were found to be blue emitters, and the solutions exhibited intense fluorescence, with a maximum of 430 nm. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 3278–3288, 2005  相似文献   
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