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201.
Crystallization and Organic Field-Effect Transistor Performance of a Hydrogen-Bonded Quaterthiophene
Dr. Jan Gebers Dr. Bilal Özen Dr. Lucia Hartmann Michel Schaer Dr. Stéphane Suàrez Philippe Bugnon Dr. Rosario Scopelliti Dr. Hans-Georg Steinrück Dr. Oleg Konovalov Prof. Andreas Magerl Dr. Martin Brinkmann Dr. Riccardo Petraglia Dr. Piotr de Silva Prof. Clémence Corminboeuf Prof. Holger Frauenrath 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(45):10265-10275
Crystalline thin films of π-conjugated molecules are relevant as the active layers in organic electronic devices. Therefore, materials with enhanced control over the supramolecular arrangement, crystallinity, and thin-film morphology are desirable. Herein, it is reported that hydrogen-bonded substituents serve as additional structure-directing elements that positively affect crystallization, thin-film morphology, and device performance of p-type organic semiconductors. It is observed that a quaterthiophene diacetamide exhibits a denser packing than that of other quaterthiophenes in the single-crystal structure and, as a result, displays enhanced intermolecular electronic interactions. This feature was preserved in crystalline thin films that exhibited a layer-by-layer morphology, with large domain sizes and high internal order. As a result, organic field-effect transistors of these polycrystalline thin films showed mobilities in the range of the best mobility values reported for single-crystalline quaterthiophenes. The use of hydrogen-bonded groups may, thus, provide an avenue for organic semiconducting materials with improved morphology and performance. 相似文献
202.
203.
PaulW. Finn Morwena Bandara Chris Butcher Angela Finn Ruth Hollinshead Nagma Khan Norman Law Sreenivasa Murthy Rosario Romero Clare Watkins Victor Andrianov RasmaM. Bokaldere Klara Dikovska Vija Gailite Einars Loza Irina Piskunova Igor Starchenkov Maxim Vorona Ivars Kalvinsh 《Helvetica chimica acta》2005,88(7):1630-1657
Inhibition of the enzyme histone deacetylase (HDAC) is emerging as a novel approach to the treatment of cancer. A series of novel sulfonamide derivatives were synthesized and evaluated for their ability to inhibit human HDAC. Compounds were identified which are potent enzyme inhibitors, with IC50 values in the low nanomolar range against enzyme obtained from HeLa cell extracts, and with antiproliferative effects in cell culture. Extensive characterization of the structure–activity relationships of this series identified key requirements for activity. These include the direction of the sulfonamide bond and substitution patterns on the central phenyl ring. The alkyl spacer between the aromatic head group and the sulfonamide functionality also influenced the HDAC inhibitory activity. One of these compounds, m 11.1 , also designated PXD101, has entered clinical trials for solid tumors and haematological malignancies. 相似文献
204.
Let C ⊂ P
3 be a smooth and connected projective curve of genus g ≥ 2. Here in characteristic ≠ 2 we prove that its generic plane section is in uniform position and that its numerical character
is connected.
Partially supported by MIUR and GNSAGA of INdAM (Italy) 相似文献
205.
Rosario Rodil Steffi Schrader Monika Moeder 《Rapid communications in mass spectrometry : RCM》2009,23(5):580-588
A comparison was made between the electrospray ionization (ESI) and atmospheric pressure photoionization (APPI) tandem mass spectrometric (MS/MS) responses of eleven ultraviolet (UV) filters. Four of the target compounds were favourably ionized in negative ion mode, and the other seven compounds in positive ion mode. For nine of the compounds APPI generated a similar response to that of ESI, but the APPI signal‐to‐noise (S/N) ratios were 1.3–60 times higher. The two most polar of the UV filter compounds (PBSA and BP‐4) were more efficiently ionized by ESI, offering higher signal intensities and lower detection limits. APPI was, however, less susceptible to ion suppression than ESI when real samples were injected. In order to optimize the APPI conditions different dopant solvents were examined to enhance the efficiency of the photoionization process. Among the evaluated dopants, toluene was selected as the best compromise. At a toluene flow rate of 10% of the solvent flow rates the ionization response increased by a factor of 40–50 over the use of no dopant for the compounds in positive ion mode and by more than 300 for the compounds in negative ion mode. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
206.
We further elaborate on the device proposed by Karimi et al. [15], in which coupled superconducting qubits can play the role of a quantum heat switch. In the present paper we analyze the performances of the switch if the number of qubits increases considering in details the cases of three and four qubits. To this aim we study the effect of the number of qubits on the transmitted power between baths. As the number of qubits increases, the transmitted power between baths increases as well. 相似文献
207.
Darío M. González Nicole B. Cruz Loreto A. Hernández Jocelyn Oyarce Rosario Benavente Carolina Manzur 《Journal of polymer science. Part A, Polymer chemistry》2020,58(4):557-567
Two Bis-β-diketonate zinc (II) complexes were synthesized using 1-(thiophen-2-yl)butane-1,3-dione and 1-(thiophen-2-yl)-3-(thiophen-3-yl)propane-1,3-dione as ligands. By electropolymerization of their thiophenyl groups, the metallopolymers deposited on FTO electrodes were obtained. The main objective was to study the reactivity of these compounds as ROP catalysts for PLA synthesis, using directly the zinc complexes (homogeneous catalysis) and also the modified electrodes with metallopolymers (heterogeneous catalysis). The homogeneous catalysis studies allowed the optimization of the polymerization conditions, such as reaction time, catalyst concentration, and the use of benzyl alcohol as cocatalyst, as well as their influence on the conversion rate, average molecular weight and polydispersity of PLA, using rac-LA and L-LA as monomers. Also, the effect on tacticity and thermal properties were discussed. Finally, the ROP studies using immersed modified electrodes in the polymerization medium were carried out under optimized experimental conditions. These tests were positive for one of the studied compounds, reaching conversions of up to 67%. © 2020 Wiley Periodicals, Inc. J. Polym. Sci. 2020 , 58, 557–567 相似文献
208.
209.
210.
Pascal Sánchez Deborah Alberts Beatriz Fernández Armando Menéndez Rosario Pereiro Alfredo Sanz-Medel 《Analytica chimica acta》2012
During the last decade the photovoltaic industry has been growing rapidly. One major strategy to reduce the production costs is the use of thin film solar cells based on hydrogenated amorphous silicon (a-Si:H). The potential of pulsed radiofrequency glow discharge coupled to optical emission spectrometry (rf-PGD-OES) for the analysis of such type of materials has been investigated in this work. It is known that when hydrogen is present in the argon discharge, even in small quantities, significant changes can occur in the emission intensities and sputtering rates measured. Therefore, a critical comparison has been carried out by rf-PGD-OES, in terms of emission intensities, penetration rates and depth resolution for two modes of hydrogen introduction in the discharge, manually external hydrogen in gaseous form (0.2% H2–Ar) or internal hydrogen, sputtered as a sample constituent. First, a comparative optimisation study (at 600 Pa and 50 W) was performed on conducting materials and on a silicon wafer varying the pulse parameters: pulse frequency (500 Hz–20 kHz) and duty cycle (12.5–50%). Finally, 600 Pa, 50 W, 10 kHz and 25% duty cycle were selected as the optimum conditions to analyse three types of hydrogenated samples: an intrinsic, a B-doped and a P-doped layer based on a-Si:H. Enhanced emission intensities have been measured for most elements in the presence of hydrogen (especially for silicon) despite the observed reduced sputtering rate. The influence of externally added hydrogen and that of hydrogen sputtered as sample constituent from the analysed samples has been evaluated. 相似文献