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951.
952.
Theoretical Vibrational Raman and Surface‐Enhanced Raman Scattering Spectra of Water Interacting with Silver Clusters 下载免费PDF全文
Marta Sanchéz‐Lozano Marcos Mandado Ignacio Pérez‐Juste Dr. Jose M. Hermida‐Ramón 《Chemphyschem》2014,15(18):4067-4076
In this study, we analyzed the Raman spectrum of a water molecule adsorbed on a cluster of 20 silver atoms, and the plasmonic electromagnetic effect of the silver surface was also considered to give a theoretical prediction of the surface‐enhanced Raman scattering spectrum. The calculations were performed at the density functional theory (DFT) level by using both frozen and unfrozen silver clusters. Two different models were used to consider the plasmonic enhancement; one of them was a modified classical (dipole) model and the other was the coupled perturbed Hartree–Fock method with excitation frequencies obtained from time‐dependent DFT calculations and with proper detuning of these frequencies. The importance of small geometrical distortions of the silver surface in the orientation of the adsorbed water was shown. Moreover, it was shown how the symmetry of the transition dipole moment and the symmetry of the vibrational modes influence the Raman intensities of the SERS spectrum. 相似文献
953.
Microwave‐Assisted Tandem Organocatalytic Peptide‐Coupling Intramolecular aza‐Michael Reaction: α,β‐Unsaturated N‐Acyl Pyrazoles as Michael Acceptors 下载免费PDF全文
Dr. María Sánchez‐Roselló Cristina Mulet Marta Guerola Dr. Carlos del Pozo Prof. Santos Fustero 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(48):15697-15701
Conjugated N‐acyl pyrazoles have been successfully employed in the organocatalytic enantioselective intramolecular aza‐Michael reaction as ester surrogates. Bifunctional squaramides under microwave irradiation provided the best results in this transformation. Furthermore, this protocol has been combined with a peptide‐coupling reaction in a tandem sequence. The final products were easily converted into the corresponding ethyl esters. 相似文献
954.
Single‐Molecule‐Magnet Behavior in the Family of [Ln(OETAP)2] Double‐Decker Complexes (Ln=Lanthanide,OETAP=Octa(ethyl)tetraazaporphyrin) 下载免费PDF全文
Nelson Giménez‐Agulló Dr. Cristina Sáenz de Pipaón Louis Adriaenssens Dr. Marta Filibian Marta Martínez‐Belmonte Eduardo C. Escudero‐Adán Prof. Pietro Carretta Prof. Pablo Ballester Prof. José Ramón Galán‐Mascarós 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(40):12817-12825
Double‐decker complexes of lanthanide cations can be readily prepared with tetraazaporphyrins (porphyrazines). We have synthesized and characterized a series of neutral double‐decker complexes [Ln(OETAP)2] (Ln=Tb3+, Dy3+, Gd3+, Y3+; OETAP=octa(ethyl)tetraazaporphyrin). Some of these complexes show analogous magnetic features to their phthalocyanine (Pc) counterparts. The Tb3+ and Dy3+ derivatives exhibit single‐molecule magnet (SMM) behavior with high blocking temperatures over 50 and 10 K, respectively. These results confirm that, in double‐decker complexes that involve Tb or Dy, the (N4)2 square antiprism coordination mode has an important role in inducing very large activation energies for magnetization reversal. In contrast with their Pc counterparts, the use of tetraazaporphyrin ligands endows the presented [Ln(OETAP)2] complexes with extraordinary chemical versatility. The double‐decker complexes that exhibit SMM behavior are highly soluble in common organic solvents, and easily processable even through sublimation. 相似文献
955.
On the Use of Metal Purine Derivatives (M=Ir,Rh) for the Selective Labeling of Nucleosides and Nucleotides 下载免费PDF全文
Marta Valencia Mamen Martín‐Ortiz Prof. Dr. Mar Gómez‐Gallego Prof. Dr. Carmen Ramírez de Arellano Prof. Dr. Miguel A. Sierra 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(13):3831-3838
The reactions of neutral or cationic IrIII and RhIII derivatives of phenyl purine nucleobases with unsymmetrical alkynes produce new metallacycles in a predictable manner, which allows for the incorporation of either photoactive (anthracene or pyrene) or electroactive (ferrocene) labels in the nucleotide or nucleoside moiety. The reported methodology (metalation of the purine derivative and subsequent marker insertion) could be used for the postfunctionalization and unambiguous labeling of oligonucleotides. 相似文献
956.
Development of a new stir bar sorptive extraction method for the determination of medium‐level volatile thiols in wine 下载免费PDF全文
Decibel Elpa Enrique Durán‐Guerrero Remedios Castro Ramón Natera Carmelo G. Barroso 《Journal of separation science》2014,37(14):1867-1872
A fast, simple, and reliable analytical method for the determination of medium‐level volatile thiols in wines is presented. Stir bar sorptive extraction using ethylene glycol‐silicone coated stir bars has been used in combination with thermal desorption gas chromatography with mass spectrometry for the analysis of 4‐mercapto‐4‐methylpentan‐2‐one, 2‐furanmethanethiol, 3‐mercaptohexyl acetate, and 3‐mercaptohexanol in wine. Optimization of the extraction technique was performed using a two‐level fractional factorial design. For the extraction step, the optimum conditions were: Ethylene glycol and silicone coated stir bars, pH at 3.5, sample volume of 25 mL, extraction time of 90 min, NaCl content 4.0 g, and stirring speed at 500 rpm. The optimized method achieved good linearity for all studied compounds (r2 > 0.995) and it provided detection limits of 21.52, 0.36, 0.73, and 2.55 μg/L for 4‐mercapto‐4‐methylpentan‐2‐one, 2‐furanmethanethiol, 3‐mercaptohexyl acetate, and 3‐mercaptohexanol, respectively. It was repeatable, with precisions lower than 18% relative standard deviation for both intraday and interday repeatability. The developed procedure is suitable for the determination of these kinds of compounds when they are present at medium concentration levels. It was finally applied to real wine samples with negative aroma derived from the high concentration levels of these compounds. 相似文献
957.
Marta Pelcová Monika Langmajerová Eliška Cvingráfová Jan Juřica Zdeněk Glatz 《Journal of separation science》2014,37(19):2785-2790
This study deals with the nonaqueous capillary electrophoretic separation of dextromethorphan and its metabolites using a methanolic background electrolyte. The optimization of separation conditions was performed in terms of the resolution of dextromethorphan and dextrorphan and the effect of separation temperature, voltage, and the characteristics of the background electrolyte were studied. Complete separation of all analytes was achieved in 40 mM ammonium acetate dissolved in methanol. Hydrodynamic injection was performed at 3 kPa for 4 s. The separation voltage was 20 kV accompanied by a low electric current. The ultraviolet detection was performed at 214 nm, the temperature of the capillary was 25°C. These conditions enabled the separation of four analytes plus the internal standard within 9 min. Further, the developed method was validated in terms of linearity, sensitivity, and repeatability. Rat liver perfusate samples were subjected to the nonaqueous capillary electrophoretic method to illustrate its applicability. 相似文献
958.
Alois Bonifacio Silvia Dalla Marta Riccardo Spizzo Silvia Cervo Agostino Steffan Alfonso Colombatti Valter Sergo 《Analytical and bioanalytical chemistry》2014,406(9-10):2355-2365
Surface-enhanced Raman spectroscopy (SERS) is a good candidate for the development of fast and easy-to-use diagnostic tools, possibly used on biofluids in point-of-care or screening tests. In particular, label-free SERS spectra of blood serum and plasma, two biofluids widely used in diagnostics, could be used as a metabolic fingerprinting approach for biomarker discovery. This study aims at a systematic evaluation of SERS spectra of blood serum and plasma, using various Ag and Au aqueous colloids, as SERS substrates, in combination with three excitation lasers of different wavelengths, ranging from the visible to the near-infrared. The analysis of the SERS spectra collected from 20 healthy subjects under a variety of experimental conditions revealed that intense and repeatable spectra are quickly obtained only if proteins are filtered out from samples, and an excitation in the near-infrared is used in combination with Ag colloids. Moreover, common plasma anticoagulants such as EDTA and citrate are found to interfere with SERS spectra; accordingly, filtered serum or heparin plasma are the samples of choice, having identical SERS spectra. Most bands observed in SERS spectra of these biofluids are assigned to uric acid, a metabolite whose blood concentration depends on factors such as sex, age, therapeutic treatments, and various pathological conditions, suggesting that, even when the right experimental conditions are chosen, great care must be taken in designing studies with the purpose of developing diagnostic tests. 相似文献
959.
Marta Leite Andreia Freitas Anabela Marisa Azul Jorge Barbosa Saul Costa Fernando Ramos 《Analytica chimica acta》2013
Amanitins, highly toxic cyclopeptides isolated from various Amanita species, are the most potent poisons accounting for the hazardous effects on intestinal epithelium cells and hepatocytes, and probably the sole cause of fatal human poisoning. 相似文献
960.
Marta F. T. Ribeiro Cristina M. C. M. Couto Pedro M. M. Conceição João L. M. Santos 《Analytical letters》2013,46(11):1769-1778
In this work, an automated multipumping pulsed flow system was implemented for the determination of phosphate in natural waters. The developed flow approach was based on the spectrophotometric determination of phosphate by using the vanadomolybdate reaction. The exploitation of a very simple manifold configuration relying on the utilization of just two active components, in this case two solenoid actuated micropumps that were accountable for sample and reagent insertion and commutation, reaction zone formation, and solutions propelling, provided a great operational and optimization simplicity, low reagent consumption, and waste minimization. Linear calibration plots for phosphate concentrations of up to 20 mg L?1 (R2 = 0.999, n = 6) were obtained, with a detection limit of 0.2 mg L?1. The sampling rate was about 60 samples per hour. The system was applied to the monitoring of phosphate in local streams at specific sampling stations. 相似文献