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991.
992.
993.
Martínez-Huitle CA Brillas E 《Angewandte Chemie (International ed. in English)》2008,47(11):1998-2005
Chlorination is the most common method worldwide for the disinfection of drinking water. However, the identification of potentially toxic products from this method has encouraged the development of alternative disinfection technologies. Among them, electrochemical disinfection has emerged as one of the more feasible alternatives to chlorination. This article reviews electrochemical systems that can contribute to drinking water disinfection and underscores the efficiency of recently developed diamond films in chlorine-free electrochemical systems. 相似文献
994.
Alexey A. Popov Dr. Natalia B. Shustova Olga V. Boltalina Dr. Steven H. Strauss Prof. Lothar Dunsch Prof. Dr. 《Chemphyschem》2008,9(3):431-438
A spectroelectrochemical study of the two isostructural asymmetric perfluoroalkyl derivatives C1‐7,24‐C70(CF3)2 and C1‐7,24‐C70(C2F5)2 is presented. Reversible formation of their stable monoanion radicals is monitored by cyclic voltammetry and by in situ ESR‐Vis‐NIR spectroelectrochemistry. The ESR spectrum of the C70(CF3)2?. radical is a 1:3:3:1 quartet with a 19F hyperfine coupling constant (a(F)) of 0.323(4) G, demonstrating that the unpaired spin is coupled to only one of the two CF3 groups. The 13C satellites are assigned to specific carbon atoms. The ESR spectrum of the C70(C2F5)2?. radical is an apparent octet with an apparent a(F) value of 0.83(2) G. DFT calculations suggest that this pattern is due to the superposition of spectra for four nearly isoenergetic C70(C2F5)2?. conformers. Time‐dependent DFT calculations suggest that the NIR band at 1090 nm exhibited by both C70(Rf)2?. radical anions is assigned to the SOMO→LUMO+3 transition. The analogous NIR band exhibited by the closed‐shell C70(CF3)22? dianion was blue‐shifted to 1000 nm. 相似文献
995.
We report a DFT study on the self‐assembly of the fullerene derivative PCBM on the Au(111) surface. Recent STM experiments (Angew. Chem. 2007 , 119, 8020–8023[1]) show a coverage‐dependent transition of the adsorption and self‐assembly of PCBM on this surface. To understand the origin of this observation, we compute the geometries and relative energies of ten PCBM dimers and four tetramers. The calculations show that the self‐assembly of PCBM at high coverage is mainly controlled by hydrogen bonding between the PCBM tails. Due to the large size of the fullerene cage, the hydrogen bonds are formed far away from the surface; hence they are very similar to those found in the gas phase. This picture successfully explains the observed site‐insensitive adsorption at high coverage and the 2D arrangement of PCBM on the surface. 相似文献
996.
Sevilla M Salinas Martínez-de Lecea C Valdés-Solís T Morallón E Fuertes AB 《Physical chemistry chemical physics : PCCP》2008,10(10):1433-1442
We present a novel and facile synthesis methodology for obtaining graphitic carbon structures from Fe(II) and Co(II) gluconates. The formation of graphitic carbon can be carried out in only one step by means of heat treatment of these organic salts at a temperature of 900 degrees C or 1000 degrees C under inert atmosphere. This process consists of the following steps: (a) pyrolysis of the organic gluconate and its transformation to amorphous carbon, (b) conversion of Fe(2+) and Co(2+) ions to Fe(2)O(3) and CoO and their subsequent reduction to metallic nanoparticles by the carbon and (c) conversion of a fraction of formed amorphous carbon to graphitic structures by Fe and Co nanoparticles that act as catalysts in the graphitization process. The removal of the amorphous carbon and metallic nanoparticles by means of oxidative treatment (KMnO(4) in an acid solution) allows graphitic carbon nanostructures (GCNs) to be selectively recovered. The GCNs thus obtained (i.e. nanocapsules and nanopipes) have a high crystallinity as evidenced by TEM/SAED, XRD and Raman analysis. In addition, we used these GCNs as supports for platinum nanoparticles, which were well dispersed (mean Pt size approximately 2.5-3.2 nm). Most electrocatalysts prepared in this way have a high electrocatalytical surface area, up to 90 m(2) g(-1) Pt, and exhibit high catalytic activities toward methanol electrooxidation. 相似文献
997.
Hortal AR Hurtado P Martínez-Haya B Arregui A Bañares L 《The journal of physical chemistry. B》2008,112(29):8530-8535
The MALDI technique with solvent-free sample preparation has been applied to evaluate relative gas-phase affinities of polyether chain polymers with alkali metal cations. The study is performed on poly(ethylene glycol) and poly(propylene glycol) polymers of different lengths (PEG600, PEG1000, PPG425, PPG750) and the alkali metal cations Li(+), Na(+), K(+), and Cs(+). The experiments show that the lattice energy of the alkali metal salts employed as cation precursors can have a strong influence on the outcome of conventional MALDI measurements. With the solvent-free method, these crystal binding effects can be made negligible by combining in the same sample alkali metal salts with different counterions. The recorded MALDI spectra show that the polyether-cation aggregation efficiencies decrease systematically with growing cation size. This cation size selectivity is considerably enhanced for the polymers with the shorter chains, which can be attributed to the reduced ability of the polymer to build a coordination shell around the larger cations. The steric effects introduced by the side CH3 group of propylene glycol with respect to ethylene glycol also enhance the preference for cationization of the polymer by the smaller cations. These observations correct some qualitative trends derived from previous studies, which did not account for lattice energy effects of the cation precursors. 相似文献
998.
The cyclam derivative 1,4,8,11-tetra(n-octyl)-1,4,8,11-tetraazacyclotetradecane (L) has been used as carrier for the preparation of PVC-based membrane ion-selective electrodes for anionic surfactants. Different membranes were prepared using L as ionophore, tetra-n-octylammonium bromide (TOAB) as cationic additive and dibutyl phthalate (DBP) or o-nitrophenyl octyl ether (NPOE) as plasticizers. The final used electrode contained a membrane of the following composition: 56% DBP, 3.4% ionophore, 3.8% TOAB and 36.8% PVC. This electrode displays a Nernstian slope of -60.0+/-0.9 mV/decade in a 2.0 x 10(-3) to 7.9 x 10(-6) mol dm(-3) concentration range and a limit of detection of 4.0 x 10(-6) mol dm(-3). The electrode can be used for 144 days without showing significant changes in the value of slope or working range. The electrode shows a selective response to dodecyl sulfate (DS-) and a poor response to common inorganic cations and anions. The selective sequence found was DS->ClO4->HCO3->SCN->NO3- approximately CH3COO- approximately I->Cl->Br->IO3- approximately NO2- approximately SO3(2-)>HPO4(2-)>C2O4(2-)>SO4(2-), i.e. basically following the Hoffmeister series except for the hydrophilic anion bicarbonate. Most of the potentiometric coefficients determined are relatively low indicating that common anions would not interfere in the DS- determination. A complete study of the response of the electrode to a family of surfactant was also carried out. The electrode showed a clear anionic response to DS- and to Na-LAS and a much poorer response to other anionic surfactants and to non-ionic surfactants. Also the electrode shows certain non-linear cationic response in the presence of cationic and zwitterionic surfactants. The electrode was used for the determination of anionic surfactants in several mixtures, and the results obtained were compared to those found using a commercially available sensor. 相似文献
999.
A new qualitative immunologically based tube test for non-instrumental detection of pyrene (PYR) in water samples was developed. The method combines the pre-concentration of analyte by immunoextraction and its detection by immunoassay using Sepharose 4B-immobilized IgG-fraction of a polyclonal anti-PYR antiserum (immunoaffinity gel) and 1-pyrenebutyric acid-horseradish peroxidase conjugate (PYR-BA-HRP). The immunoaffinity gel was placed in a standard 1-ml SPE column through which a 10-ml aliquot of water sample spiked with 10% acetonitrile was passed. Following, free antibody binding sites were detected by application of PYR-BA-HRP. Four minutes after addition of the chromogenic substrate the results were visually evaluated by occurring or stayed away blue colour development for negative and positive samples, respectively. Total time for assay was about 15 min for six samples. Under optimized conditions a cut-off level for pyrene of 0.04 ng ml(-1) was found. At this defined concentration, a set of spiked samples (n=175) was analyzed and very low rates of false negatives (1.2%) and false positives (4.6%) determined which fulfils the requirement set by Commission Decision 2002/657/EC for a screening method. No interference by other PAH compounds like naphthalene, fluoranthene, phenanthrene, anthracene, and benzo[a]pyrene at a concentration of 20 ng ml(-1), i.e., 500-fold excess compared to the defined cut-off level was observed. Different water types like surface water, tap water, bottled water, and melted snow were analyzed for PYR contamination by the proposed method and results confirmed by HPLC-FLD. 相似文献
1000.
Carbon screen-printed electrodes (CSPEs) modified with metal nanoparticles present an interesting alternative in the determination of chromium(VI) by differential pulse voltammetry (DPV).Metallic silver and gold nanoparticle deposits have been obtained by electrochemical deposition. Scanning electron microscopy measurements show that the electrochemically synthesized silver and gold nanoparticles are deposited in aggregated form.The detection limit for the analytical procedures developed in this work were 8.5 × 10−7 and 4.0 × 10−7 M for silver and gold nanoparticle-modifed CSPE, respectively.In terms of reproducibility, the precision of the above-mentioned method was calculated at 6.7% in %R.S.D. values for silver and 3.21% for gold nanoparticle CSPE. 相似文献