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81.
Miroslaw Pluta Marie‐Amlie Paul Michaël Alexandre Philippe Dubois 《Journal of Polymer Science.Polymer Physics》2006,44(2):299-311
Polylactide (PLA)‐layered silicate nanocomposites plasticized with 20 wt % of poly(ethylene glycol) 1000 were prepared by melt blending. Three kinds of organo‐modified montmorillonites—Cloisite® 20A, Cloisite® 25A, and Cloisite® 30B—were used as fillers at a concentration level varying from 1–10 wt %. Neat PLA and plasticized PLA with the same thermomechanical history were considered for comparison. Nanocomposites based on amorphous PLA were obtained via melt‐quenching. The influence of both plasticization and nanoparticle filling on the physicochemical properties of the nanocomposites were investigated. Characterization of the systems was achieved by size exclusion chromatography (SEC), thermogravimetric analysis (TGA), thermally modulated differential scanning calorimetry (TMDSC), X‐ray diffraction (XRD), and dynamic mechanical analysis (DMTA). SEC revealed a decrease of the molecular weight of the PLA matrix with the filler content. Thermal behavior on heating showed one cold crystallization process in the reference neat PLA sample, while two cold crystallization processes in plasticized PLA and plasticized nanocomposites. The thermal windows of these processes tend to increase with the filler content. The crystalline form of PLA developed upon heating was affected neither by the plasticization nor by the type and content of Cloisite used. It was found that the series of organo‐modified montmorillonites with decreasing affinity to PLA is Cloisite® 30B, Cloisite® 20A, and Cloisite® 25A, respectively. The dynamic mechanical properties were sensitive to the sample composition. Generally, the storage modulus increased with the filler content. Glassy PEG, well dispersed within unfilled PLA matrix, exhibited also a reinforcing effect, since the storage modulus of this sample was higher than for unplasticized reference at temperature region below the glass transition of PEG. Moreover, loss modulus of all plasticized samples revealed an additional maximum ascribed to the glass transition of PEG–rich dispersed phase, indicating partial miscibility of organic components of the systems investigated. The magnitude of this mechanical loss was correlated with the filler content, and to some extent, also with the nanofiller ability to be intercalated by polymer components. © 2005 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 299–311, 2006 相似文献
82.
Gabi Schierning Miroslaw Batentschuk Andres Osvet Albrecht Winnacker 《Radiation measurements》2004,38(4-6):529-532
The undoped stoichiometric materials LiTbP4O12 and LiEuP4O12 show effective green Tb3+ and red Eu3+ luminescence, respectively. Both systems are fully mixable, which offers the possibility of examining the energy transfer from Tb3+ to Eu3+ in the complete system of LiTb1−xEuxP4O12. As the distance of the rare earth ions is large enough to exclude exchange interaction in these materials, only multipolar interaction is to be expected. Dealing only with forbidden f–f transitions it is possible to produce both Tb3+ and Eu3+ luminescence at the same time having a suitable Eu3+ concentration. 相似文献
83.
Biological activity of 5-aminolevulinic acid and its methyl ester after storage under different conditions 总被引:1,自引:0,他引:1
Kaliszewski M Kwasny M Juzeniene A Juzenas P Graczyk A Ma LW Iani V Mikolajewska P Moan J 《Journal of photochemistry and photobiology. B, Biology》2007,87(2):67-72
5-Aminolevulinic acid (ALA) is a natural precursor of protoporphyrin IX (PpIX) and heme in cells. Photodynamic therapy (PDT) utilizes a metabolic imbalance in cancer cells, leading to increased PpIX generation from exogenous ALA. Due to chemical instability of ALA in therapeutic concentrations at pH values larger than 5.0 and at high temperatures, it looses its activity by spontaneous dimerization to 2,5-dicarboxyethyl-3,6-dihydropyrazine (DHPY). ALA esters are now supplementing ALA in PDT, but little is known about their stability. We have studied the stability of ALA and its methyl ester (MAL) stored under different conditions (temperatures, pH values) by measuring their ability to generate PpIX. 100mM solutions of both compounds were found to be stable at pH 4 and at 4 degrees C. However, at pH 5.5 they lost almost 10% of the initial activity during 5days of storage at 4 degrees C. The fastest decay of ALA and MAL was seen at pH 7.4 and at 37 degrees C, and followed first order kinetics. At pH 7.4 and at 4 degrees C MAL lost its PpIX producing ability more slowly than at 37 degrees C. Our work shows that solutions should be prepared immediately before use and stored at low temperatures. The pH of stock solutions should not exceed 5. 相似文献
84.
Miroslaw J. Tomaszewski 《Tetrahedron letters》2008,49(19):3172-3175
A one-pot synthesis of the 2,3-dihydro-1H-pyrrolo[3,2-c]quinoline core from substituted 2-iodoanilines and 2,3-dihydro-1H-pyrrole was achieved using 10 mol % Pd(PPh3)4, and K2CO3 in 1,4-dioxane at 170 °C for 1 h in a microwave oven. This reaction can be carried out on a gram scale. The proposed mechanism involves a Heck-coupling reaction followed by intra-molecular Schiff base formation and double bond migration. 相似文献
85.
Olga Perzanowska Dr. Miroslaw Smietanski Prof. Jacek Jemielity Dr. Joanna Kowalska 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(42):e202201115
Poly(A)-binding protein (PABP) is an essential element of cellular translational machinery. Recent studies have revealed that poly(A) tail modifications can modulate mRNA stability and translational potential, and that oligoadenylate-derived PABP ligands can act as effective translational inhibitors with potential applications in pain management. Although extensive research has focused on protein-RNA and protein-protein interactions involving PABPs, further studies are required to examine the ligand specificity of PABP. In this study, we developed a microscale thermophoresis-based assay to probe the interactions between PABP and oligoadenylate analogs containing different chemical modifications. Using this method, we evaluated oligoadenylate analogs modified with nucleobase, ribose, and phosphate moieties to identify modification hotspots. In addition, we determined the susceptibility of the modified oligos to CNOT7 to identify those with the potential for increased cellular stability. Consequently, we selected two enzymatically stable oligoadenylate analogs that inhibit translation in rabbit reticulocyte lysates with a higher potency than a previously reported PABP ligand. We believe that the results presented in this study and the implemented methodology can be capitalized upon in the future development of RNA-based biological tools. 相似文献
86.
87.
Marcin Bienkowski Jaroslaw Byrka Miroslaw Korzeniowski Friedhelm Meyer auf der Heide 《Journal of Discrete Algorithms》2009,7(4):545-569
We present an extension of a classical data management subproblem, the page migration. The problem is investigated in dynamic networks, where costs of communication between different nodes may change with time. We construct asymptotically optimal online algorithms for this problem, both in deterministic and randomized scenarios. 相似文献
88.
Gruszkiewicz MS Rother G Wesolowski DJ Cole DR Wallacher D 《Langmuir : the ACS journal of surfaces and colloids》2012,28(11):5070-5078
The densities of pore-confined fluids were measured for the first time by means of vibrating tube densimetry (VTD). A custom-built high-pressure, high-temperature vibrating tube densimeter was used to measure the densities of propane at subcritical and supercritical temperatures (between 35 and 97 °C) and carbon dioxide at supercritical temperatures (between 32 and 50 °C) saturating hydrophobic silica aerogel (0.2 g/cm(3), 90% porosity) synthesized inside Hastelloy U-tubes. Additionally, supercritical isotherms of excess adsorption for CO(2) and the same porous solid were measured gravimetrically using a precise magnetically coupled microbalance. Pore fluid densities and total adsorption isotherms increased monotonically with increasing density of the bulk fluid, in contrast to excess adsorption isotherms, which reached a maximum and then decreased toward zero or negative values above the critical density of the bulk fluid. The isotherms of confined fluid density and excess adsorption obtained by VTD contain additional information. For instance, the maxima of excess adsorption occur below the critical density of the bulk fluid at the beginning of the plateau region in the total adsorption, marking the end of the transition of pore fluid to a denser, liquidlike pore phase. Compression of the confined fluid significantly beyond the density of the bulk fluid at the same temperature was observed even at subcritical temperatures. The effect of pore confinement on the liquid-vapor critical temperature of propane was less than ~1.7 K. The results for propane and carbon dioxide showed similarity in the sense of the principle of corresponding states. Good quantitative agreement was obtained between excess adsorption isotherms determined from VTD total adsorption results and those measured gravimetrically at the same temperature, confirming the validity of the vibrating tube measurements. Thus, it is demonstrated that vibrating tube densimetry is a novel experimental approach capable of providing directly the average density of pore-confined fluids, and hence complementary to the conventional gravimetric or volumetric/piezometric adsorption techniques, which yield the excess adsorption (the Gibbsian surface excess). 相似文献
89.
Bosco EE Kumar S Marchioni F Biesiada J Kordos M Szczur K Meller J Seibel W Mizrahi A Pick E Filippi MD Zheng Y 《Chemistry & biology》2012,19(2):228-242
The NADPH oxidase enzyme complex, NOX2, is responsible for reactive oxygen species production in neutrophils and has been recognized as a key mediator of inflammation. Here, we have performed rational design and in?silico screen to identify a small molecule inhibitor, Phox-I1, targeting the interactive site of p67(phox) with Rac GTPase, which is a necessary step of the signaling leading to NOX2 activation. Phox-I1 binds to p67(phox) with a submicromolar affinity and abrogates Rac1 binding and is effective in inhibiting NOX2-mediated superoxide production dose-dependently in human and murine neutrophils without detectable toxicity. Medicinal chemistry characterizations have yielded promising analogs and initial information of the structure-activity relationship of Phox-I1. Our studies suggest the potential utility of Phox-I class inhibitors in NOX2 oxidase inhibition and present an application of rational targeting of a small GTPase-effector interface. 相似文献
90.
Ehlert O Osvet A Batentschuk M Winnacker A Nann T 《The journal of physical chemistry. B》2006,110(46):23175-23178
A novel organometallic synthesis method for the preparation of colloidal ZnS nanoparticles is presented. This method enables the synthesis of undoped ZnS nanocrystals as well as doping with Cu, Pb, or both. The particles can be covered with an undoped layer of ZnS, forming core/shell-type particles with the ZnS:Pb, ZnS:Cu, or ZnS:Cu,Pb cores. The particles were characterized via TEM, XRD, dynamic light scattering, and optical spectroscopy. We investigated the extrinsic surface defects and their coverage with an additional ZnS layer in detail by temperature-dependent luminescence and luminescence lifetime spectroscopy. 相似文献