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61.
J. A. M. S. Duarte 《Zeitschrift für Physik B Condensed Matter》1990,80(2):299-304
A method for conversion of directed site animals to their bond counterparts is used to significantly extend the number of such configurations in 2, 3, 4 dimensions, obtain their loop partition and study the singularity structure (for both dominant and subdominant singularities) of the corresponding dilute polymer transitions. A special property of bond directed configurations (equivalence lence of loop and bond perimeter partition) is exploited to obtain longer susceptibility series in 3 and 4 dimensions and the gap exponent estimate is refined into the intervals TANOPartly funded by SBF 341 (Aachen-Julich-Koln) and Reitoria Uni. Porto (Project 1-87) 相似文献
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Ftima C. Teixeira Carla Lucas M. Joo M. Curto Antnio P. S. Teixeira M. Teresa Duarte Vnia Andr 《Heteroatom Chemistry》2016,27(1):3-11
Novel tetraethyl ethylene‐1,1‐bisphosphonate esters derived from 1H‐indazole, 1H‐pyrazolo[3,4‐b]pyridine, and 1H‐pyrazolo[3,4‐b]quinoline were synthesized by a Michael addition reaction of tetraethyl ethylidene‐1,1‐bisphosphonate with the corresponding heterocycle, using conventional heating and microwave‐assisted methods. The microwave‐assisted method provides shorter reaction times and better yields. The hydrolysis of bisphosphonates afforded the corresponding bisphosphonic acids or salt, using concentrated hydrochloric acid or TMSBr/collidine, respectively. All new compounds were fully characterized, and their structures were assigned using 1H, 31P, and 13C NMR and IR spectroscopies and mass spectrometry. The molecular structure of compound 6 was confirmed by X‐ray diffraction studies. 相似文献
64.
Batalioto F Martins OG Duarte AR Figueiredo Neto AM 《The European physical journal. E, Soft matter》2011,34(1):10
In this work we investigate the influence of the adsorption of ions on the impedance spectroscopy of an electrolytic cell.
We consider that the positive and negative ions present in a dielectric liquid are adsorbed in the electrode surfaces with
different adsorption energies. This difference in adsorption energies causes an additional plateaux in the limit of the low-frequency
range of the real part of the impedance Z . In the same frequency range, a second minimum in the imaginary part of Z is predicted. The theory is illustrated with measurements of the impedance of an electrolytic solution in the frequency range
from 10-2Hz to 1KHz. A comparison between the present model and others from the literature to describe the experimental results is
also made. 相似文献
65.
Eduardo de Almeida Paulo Rogério Massoni Amauri Antonio Menegário Laudi Cunha Leite Dante Pazzanese Duarte Lanna Virgílio Franco do Nascimento Filho 《X射线光谱测定》2011,40(6):424-426
This article describes a comparison of conventional energy‐dispersive X‐ray fluorescence (EDXRF) and synchrotron radiation total‐reflection X‐ray fluorescence (SRTXRF) for Co determination in ruminal fluid from Holstein cow. This element is used as marker for animal nutrition studies. For EDXRF, 200 µl of the sample were dried on 6.35 µm Mylar film at 60 °C. The excitation was carried out using an X‐ray tube with Mo target and Zr filter operated at 30 kV/20 mA. For SRTXRF, 10 µl of the sample were pipetted on a Lucite carrier and dried at 60 °C. In both the techniques, Ga was used as internal standard and the acquisition time was 200 s. The trueness of both techniques was evaluated through the standard addition method, the recoveries obtained by SRTXRF and EDXRF were 76 and 99%, and the limits of detection, 13 and 240 µg l?1, respectively. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
66.
Vicente Campos Rafael Martí Jesús Sánchez-Oro Abraham Duarte 《The Journal of the Operational Research Society》2014,65(12):1800-1813
In this paper, we address an optimization problem resulting from the combination of the well-known travelling salesman and knapsack problems. In particular, we target the orienteering problem, originated in the context of sport, which consists of maximizing the total score associated with the vertices visited in a path within the available time. The problem, also known as the selective travelling salesman problem, is NP-hard and can be formulated as an integer linear program. Since the 1980s, several solution methods for this problem have been developed and applied to a variety of fields, particularly in routing and tourism. We propose a heuristic method—based on the Greedy Randomized Adaptive Search Procedure (GRASP) and the Path Relinking methodologies—for finding approximate solutions to this optimization problem. We explore different constructive methods and combine two neighbourhoods in the local search of GRASP. Our experimentation with 196 previously reported instances shows that the proposed procedure obtains high-quality solutions employing short computing times. 相似文献
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Couto N Duarte MF Fernandez MT Rodrigues P Barros MT Costa ML Cabral BJ 《Journal of the American Society for Mass Spectrometry》2007,18(3):453-465
Most complexes of azides and transition metals involve the N(3)(-) azide anion as a ligand other than an organic azide. Complexes of organic azides with metals are involved in biological applications and in the deposition of nitrenes on metal surfaces, producing nitride layers for semi-conductors preparation; this makes the study of these interactions an important issue. This work describes a study of the complexation of nickel and cobalt by 3-azidopropionitrile by means of electrospray ionization mass spectrometry (ESI-MS). Complexes were obtained from solutions of NiCl(2) and CoCl(2) in methanol/water. In the case of nickel, other NiX(2) salts were investigated (where X = Br or NO(3)) and other solvents were also studied (notably ethanol/water). All complexes detected were single positively charged, with various stoichiometries, some resulted from the fragmentation of the ligand, the loss of N(2), and HCN being quite common. The most abundant cations observed were [Ni(II)AzAzX](+), where X = Cl, Br, NO(3). Some of the complexes showed solvation with methanol/ethanol/water. Metal reduction was observed in complexes where a radical was lost, resulting from the homolytic cleavage of a metal-nitrogen bond. Collision induced dissociation (CID) experiments followed by tandem mass spectrometry (MS-MS) analysis were not absolutely conclusive about the coordination site. However, terminal ions observed from the fragmentation routes were explained by a proposed gas-phase mechanism. Density functional theory calculations were carried out and provided structures for some complexes, pointing to the possibility of 3-azidopropionitrile acting as a mono- or a bidentate ligand. 相似文献
70.
Structurally Defined αMHC‐II Nanobody–Drug Conjugates: A Therapeutic and Imaging System for B‐Cell Lymphoma 下载免费PDF全文
Dr. Tao Fang Dr. Joao N. Duarte Jingjing Ling Zeyang Li Jonathan S. Guzman Prof. Dr. Hidde L. Ploegh 《Angewandte Chemie (International ed. in English)》2016,55(7):2416-2420
Antibody–drug conjugates (ADCs) of defined structure hold great promise for cancer therapies, but further advances are constrained by the complex structures of full‐sized antibodies. Camelid‐derived single‐domain antibody fragments (VHHs or nanobodies) offer a possible solution to this challenge by providing expedited target screening and validation through switching between imaging and therapeutic activities. We used a nanobody (VHH7) specific for murine MHC‐II and rendered “sortase‐ready” for the introduction of oligoglycine‐modified cytotoxic payloads or NIR fluorophores. The VHH7 conjugates outcompeted commercial monoclonal antibodies (mAbs) for internalization and exhibited high specificity and cytotoxicity against A20 murine B‐cell lymphoma. Non‐invasive NIR imaging with a VHH7–fluorophore conjugate showed rapid tumor targeting on both localized and metastatic lymphoma models. Subsequent treatment with the nanobody–drug conjugate efficiently controlled tumor growth and metastasis without obvious systemic toxicity. 相似文献