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161.
Tülay. Bal. Demirci Yüksel Köseoğlu Sadik Güner Bahri Ülküseven 《Central European Journal of Chemistry》2006,4(1):149-159
Four new oxovanadium(IV) compounds were prepared by template reaction of salicyl-, 5-bromosalicyl-and 3-methoxysalicyl-aldehyde
S-methylthiosemicarbazones with 2-hydroxy-, 5-bromo-2-hydroxy-and 3-methoxy-2-hydroxy-benzaldehyde in various combinations.
The compounds were isolated as stable solid compounds with general formula [VO(L)] and characterized by elemental analysis,
conductivity and magnetic measurements, electronic, IR and EPR spectroscopy. The X-band EPR signals recorded from powder forms
of all samples have a single asymmetric line shape and theoretical fit studies proved the presence of axial symmetry around
the paramagnetic vanadium ions. The anisotropic Lande splitting factors take values of g‖ < g⊥ < ge = 2.0023. Orbital energy levels for magnetic electrons were determined from theoretically well fitted Spin Hamiltonian parameters.
The EPR spectra recorded from solution forms almost have isotropic character. 相似文献
162.
Cansu Uzaras Uğur Avcıbaşı Hasan Demiroğlu Emin İlker Medine Ayfer Yurt Kılçar Fazilet Zümrüt Biber Müftüler Perihan Ünak 《Journal of Radioanalytical and Nuclear Chemistry》2016,307(1):131-140
The aim of this study is to determine the incorporations of PHT radiolabeled with 131I (131I-PHT) on U-87 MG, Daoy and A549 cancerous cell lines. For this, cold and radio-labeling studies were carried out. The radio-labeling yield of 131I-PHT was obtained about 95 %. Subsequently, cell culture studies were carried out and radio-labeling yields of 131I, 131I-PHT on U-87 MG, Daoy and A549 cancerous cells were investigated. Cell culture studies demonstrated that the incorporation values of 131I-PHT on the three cell lines decreased with increasing radioactivity. Consequently, 131I-PHT may be a good radiopharmaceutical for targeting radionuclide therapy of Central Nervous System Tumors. 相似文献
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165.
Highly swollen hydrogels made by the polymerization of acrylamide (AAm) with some anionic monomers such as citraconic acid (CITA) and sodium acrylate (SA) were investigated as a function of composition to find materials with swelling and dye sorption properties. Highly swollen AAm/CITA/SA or AAm/SA/CITA hydrogels were prepared by free radical solution polymerization in aqueous solutions of AAm with CITA and SA as co‐monomers and two multifunctional crosslinkers such as ethylene glycol dimethacrylate (EGDMA) and 1,4‐butanediol dimethacrylate (BDMA). Swelling experiments were performed in water at 25°C, gravimetrically. Chemically crosslinked AAm/CITA/SA or AAm/SA/CITA hydrogels were used in experiments on sorption of water‐soluble monovalent cationic dye such as “Nil blue” (Basic Blue 12; BB 12). Equilibrium percentage swelling values of AAm/CITA/SA or AAm/SA/CITA hydrogels were calculated in the range of 1797–22,098%. Some swelling kinetic parameters were found. Diffusion behavior of water was investigated. Water diffusion into the hydrogels was found to be non‐Fickian in character. For sorption of cationic dye, BB 12 into the hydrogels was studied by batch sorption technique at 25°C. AAm/CITA/SA or AAm/SA/CITA hydrogels in the dye solutions showed coloration, whereas AAm hydrogel did not show sorption of any dye from the solution. The sorption capacity of AAm/CITA/SA or AAm/SA/CITA hydrogels was investigated. At the end of the experiments, 21.70–78.91% BB 12 adsorptions were determined. Copyright © 2007 John Wiley & Sons, Ltd. 相似文献
166.
İlknur Üstündağ Aslı Erkal Tamer Koralay Yusuf Kağan Kadıoğlu Seungwon Jeon 《Journal of Analytical Chemistry》2016,71(7):685-695
We obtained a gold nanomaterial/graphene oxide-modified glassy carbon electrode and characterized it using transmission electron microscope, scanning electron microscope, cyclic voltammetry (CV), and X-ray photoelectron spectroscopy techniques. A response of the electrode using square wave anodic stripping voltammetry for Pb2+, Cu2+, and Hg2+ was found linear in the range from 1 × 10–7 to 1 × 10–11 M. The detection limits of Pb2+, Cu2+ and Hg2+ were 0.14, 0.5 and 1.2 pM, respectively. The method was applied to the simultaneous determination of Pb2+, Cu2+ and Hg2+ in seawater samples from a coastal region of Anatolia, and the results corresponded well with the values obtained by inductively coupled plasma-optical emission spectroscopy. 相似文献
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168.
In this study, structural and optoelectronic properties and photodedection characteristics of diodes constructed from p-zinc telluride (ZnTe) thin film/n-silicon (Si) nanowire heterojunctions are reported. Dense arrays of vertically aligned Si nanowires were successfully synthesized on (1 1 0)-oriented n-type single crystalline Si wafer using simple and inexpensive metal-assisted etching (MAE) process. Following the nanowire synthesis, p-type ZnTe thin films were deposited onto vertically oriented Si nanowires via radio frequency magnetron sputtering to form three-dimensional heterojunctions. A comparative study of the structural results obtained from X-ray diffraction and Raman spectroscopy measurements showed the improved crystallinity of the ZnTe thin films deposited onto the Si nanowire arrays. The fabricated nanowire-based heterojunction devices exhibited remarkable diode characteristics and enhanced optoelectronic properties and photosensitivity in comparison to the planar reference. The electrical measurements revealed that the diodes with nanowires had a well-defined rectifying behaviour with a rectification ratio of 104 at ±2 V and a relatively small ideality factor of n = 1.8 with lower reverse leakage current and series resistance at room temperature in dark condition. Moreover, an open-circuit voltage of 100 mV was also observed under illumination. Based on spectral photoresponsivity measurements, the nanowire-based device exhibited a distinct responsivity and high detectivity in visible and near-infrared (NIR) wavelength regions. The device characteristics observed here offer that the fabricated ZnTe thin film/Si nanowire-based p–n heterojunction structures will find important applications in future and will be a promising candidate for high-performance and low-cost optoelectronic device applications, NIR photodedectors in particular. 相似文献
169.
Accurate analysis of samples is very important for scientists working in many fields. XRF device is used very frequently especially in mine analysis. However, researchers are trying to reach accurate results with many different analysis methods. In addition to the known analysis methods, alternative research methods also guide the studies. In this study, two barite ore samples, collected from two regions of different nature (Denizli and Akda?madeni) by following specified sampling methods, were analyzed using Confocal Raman Spectroscopy (CRS) and Polarized Energy Dispersive X-Ray Fluorescence (PEDXRF) spectrometer. The first sample was from a metamorphic basement, and the second was from an alkali syenite rock unit. The main objective of this paper is to compare the optical characteristics of these two different barite samples collected from different regions under a polarized microscope, using CRS and PEDXRF. The results of polarized microscopy analysis showed that the barite taken from Denizli is associated with calcite. On the other hand, the barite taken from Akda?madeni is associated with galena, celestite, and quartz. Two different colors were observed in the barite samples. CRS and PEDXRF results showed that the barites collected from two regions differed in mineral association, chemical composition, and physical properties. The accuracy of the chemical analysis technique was ensured by following USGS standards, GBW 7109, and GBW-7309 Sediment. Barite ores were analyzed using HR-800 (HORIBA-Jobin Yvon) CRS and a polarized microscope (Leica DMLP). Thanks to this study, it has been shown that mineral analyzes can be performed with an accuracy close to XRF with Confocal Raman spectroscopy. Confocal Raman spectroscopy will also guide researchers for mineral analysis. 相似文献
170.
The molecular structure of 1,2,4-triazole containing thiophene derivative which called as ethyl-2-(4-amino-5-oxo-3-(thiophene-2-ylmethyl)-4,5-dihydro-1,2,4-triazole-1-yl) acetate (I) was optimized using DFT/B3LYP method with 6–311++G(d,p) basis set and the structural parameters of the compound were obtained. Thus, the molecular structure was compared with that identified by X-ray analysis. IR and NMR parameters were calculated by DFT/B3LYP/6–311++G(d,p) method. Theoretical vibrational frequencies and NMR chemical shift values were obtained. In addition, the molecular electrostatic potential (MEP) map was calculated. The structural and spectral data obtained from the theoretical study strongly confirm the experimental data. The compatibility of the structural parameters reveal that the choice of the method and the basis function is appropriate. 相似文献