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排序方式: 共有126条查询结果,搜索用时 312 毫秒
1.
A Raney-Ag catalyst was prepared by leaching out aluminium from a Raney Ag-Al alloy with NaOH solution. The kinetics of leaching
has been investigated in a stirred-batch-reactor at various temperatures by using alloy particles of different sizes. The
kinetic model best fitting the experimental results has been determined.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
2.
Pd(II)-exchanged NaY zeolite showed high activity in the Suzuki cross-coupling reactions of aryl bromides and iodides without added ligands. The DMF:water ratio, and the type and amount of base were found to be critical for the efficiency of the reaction. The catalyst is reusable after regeneration. 相似文献
3.
Antimicrobial activity studies of the binuclear metal complexes derived from tridentate Schiff base ligands 总被引:1,自引:0,他引:1
Tümer Mehmet Köksal Hüseyin Sener M. Kasim Serin Selahattin 《Transition Metal Chemistry》1999,24(4):414-420
Three novel tridentate Schiff base ligands derived fromthe 3-hydroxysalicylaldehyde (H2L1), 4-hydroxysalicylaldehyde (H2L2) and 5-bromosalicylaldehyde (H2L3) with a new amine N-(pyridyl)-2-hydroxy-3-methoxy-5-aminobenzylamine (2) have been prepared. The ligands and their metal complexes have been characterized by elemental analyses, conductivity and magnetic susceptibility measurements, i.r., electronic absorption and 1H and 13C n.m.r. spectroscopy. All complexes are binuclear and, in some, the H2O molecules are coordinated to the metal ion. Antimicrobial activities of the ligands and their complexes have been tested against to the Bacillus subtilis IMG 22 (bacteria), Micrococcus luteus LA 2971 (bacteria) Saccharamyces cerevisiae WET 136 (yeast), and Candida albicans CCM 314 (yeast). Thermal properties of all complexes have been studied by t.g. and d.t.a techniques. 相似文献
4.
In this study, the Schiff base ligands H2L1–H2L3 and their CuII, CoII, NiII, FeIII RuIII and VOIV complexes have been prepared and characterized by spectroscopic and analytical techniques. All the complexes are mononuclear.
Keto-enol tautomeric forms of the ligands have been investigated in polar and apolar solvents. The ligands favor the keto-form
in the C7H8 and C6H14. The C–C coupling reaction of the 2,6-di-t-butylphenol has been investigated by the CoII and CuII complexes. Thermal properties of the complexes have been assessed using thermal techniques and similar properties were found.
In the FeIII and RuIII complexes, firstly, the coordinated water molecule is lost from the complex; in the second step, the chloride ion leaves
the molecule in the 300–350 °C temperature range. Finally, the complexes decompose to the appropriate metal oxide at the higher
temperature ranges. The electrochemical properties of the complexes have been studied in the two different solvents (DMF and
CH3CN). 相似文献
5.
Electrochemical studies of famotidine were carried out using voltammetric techniques: cyclic voltammetry, linear sweep and square wave adsorptive stripping voltammetry. The dependence of the current on pH, buffer concentration, nature of the buffer, and scan rate was investigated. The best results for the determination of famotidine were obtained in MOPS buffer solution at pH 6.7. This electroanalytical procedure enabled to determine famotidine in the concentration range 1 × 10−9–4 × 10−8 mol L−1 by linear sweep adsorptive stripping voltammetry (LS AdSV) and 5 × 10−10–6 × 10−8 mol L−1 by square wave adsorptive stripping voltammetry (SW AdSV). Repeatability, precision and accuracy of the developed methods were checked. The detection and quantification limits were found to be 1.8 × 10−10 and 6.2 × 10−10 mol L−1 for LS AdSV and 4.9 × 10−11 and 1.6 × 10−10 mol L−1 for SW AdSV, respectively. The method was applied for the determination of famotidine in urine. 相似文献
6.
The effects of polyelectrolytes on the inhibition and aggregation of calcium oxalate crystallization
The influence of polyelectrolytes with different architecture on spontaneous batch crystallization of calcium oxalate was investigated. A series of acidic acrylate block copolymers were been made, by radical polymerization, with defined molecular weight and structure. Radical polymerization of acrylic acid (AA) was carried out in the presence of α‐thiopolyethylene glycol monomethylether as a chain transfer agent to produce poly(ethylene glycolblockacrylic acid) copolymers. Poly(ethylene glycol) (PEG) block length in the copolymers was controlled by using three different molecular weight chain transfer agents (Mn = 350, 750 and 2000 g/mol). The presence of copolymers inhibited the crystal growth of calcium oxalate possibly through adsorption onto the active growth sites for crystal growth due to the charge and hydrophilic effects. Copyright © 2006 John Wiley & Sons, Ltd. 相似文献
7.
Deniz Sinirlioglu Ali Ekrem Muftuoglu Kurtulus Golcuk Ayhan Bozkurt 《Journal of polymer science. Part A, Polymer chemistry》2014,52(13):1885-1897
This work uses a simple “grafting through” approach in the preparation of anhydrous poly(vinylidene fluoride) (PVDF)‐g‐PVTri polymer electrolyte membranes (PEMs). Alkaline‐treated PVDF was used as a macromolecule in conjunction with vinyltriazole in the graft copolymerization. The obtained polymer was subsequently doped with triflic acid (TA) at different stoichiometric ratios with respect to triazole units and the anhydrous PEMs (PVDF‐g‐PVTri‐(TA)x) were prepared. All samples were characterized by FTIR and 1H NMR. The composition of PVDF‐g‐PVTri was determined by energy dispersive spectroscopy. Thermal properties of the membranes were examined by thermogravimetric analysis and differential scanning calorimetry. The surface roughness and morphology of the membranes were studied using atomic force microscopy, X‐ray diffraction, and scanning electron microscopy. PVDF‐g‐PVTri‐(TA)3 (C3‐TA3) with a degree of grafting of 47.22% showed a maximum proton conductivity of 0.09 S cm?1 at 150 °C and anhydrous conditions. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 1885–1897 相似文献
8.
Damla Durak Anıl Delikanlı Cahit Demetgül İbrahim Kani Selahattin Serin 《Transition Metal Chemistry》2013,38(2):199-206
An unsymmetrical tetradentate Schiff base (H2L) was synthesized by the reaction of 3-methoxysalicylaldehyde, o-phenylenediamine, and salicylaldehyde in EtOH. H2L was characterized by single-crystallographic X-ray analysis. Its Co(II) and Mn(III) complexes ([CoL] and [MnLCl]) were prepared and immobilized on 3-aminopropyltriethoxysilane functionalized silica gel. The immobilized materials were found to be efficient catalysts for epoxidation of styrene in the presence of tert-BuOOH in acetonitrile at 40 °C. The catalysts can be reused several times without significant loss of performance. 相似文献
9.
Theoretical and Mathematical Physics - The partition functions of three-dimensional N=2 supersymmetric gauge theories on different manifolds can be expressed as q-hypergeometric integrals.... 相似文献
10.