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991.
Potential Analysis - We prove Wasserstein distance bounds between the probability distributions of stochastic integrals with jumps, based on the integrands appearing in their stochastic integral... 相似文献
992.
Fabio Martinelli 《Journal of statistical physics》1992,66(5-6):1245-1276
We present results on the Swendsen-Wang dynamics for the Ising ferromagnet in the low-temperature case without external field in the thermodynamic limit. We discuss in particular the rate of convergence to the equilibrium Gibbs state in finite and infinite volume, the absence of ergodicity in the infinite volume, and the long-time behavior of the probability distribution of the dynamics for various starting configurations. Our results are purely dynamical in nature in the sense that we never use the reversibility of the process with respect to the Gibbs state, and they apply to a stochastic particle system withnon- Gibbsian invariant measure. 相似文献
993.
Laura Pigani Renato Seeber Fabio Terzi Chiara Zanardi 《Journal of Electroanalytical Chemistry》2004,570(2):235-242
Electrogenerated deposits of poly[4,4′-bis(butylsulphanyl)-2,2′-bithiophene] have been characterised in the presence of different supporting electrolytes, by coupling current (charge) to microgravimetric measurements from the electrochemical quartz crystal microbalance (EQCM). The simultaneous collection of voltammetric measurements and of data relative to mass changes shows the influence exerted by the nature of the supporting electrolyte on the charge-discharge steps of both p- and n-doping processes. Interestingly, the microgravimetric data collected corresponding to the pre-peaks of both doping processes suggest the occurrence of two opposite motions of ions (ingress into and exit out from the polymer) in the relevant potential region, giving a contribution to the study of the `residual charge' phenomenon. 相似文献
994.
Optical emission and Fourier transform infrared absorption diagnostics have been carried out in hexamethyldisiloxane/oxygen RF discharges for studying the effects of the feed composition and the power on the deposition of SiO2—like thin films. Ex situ FTIR absorption has been utilized to monitor organic moieties and silanol groups in the film. It is shown that carbon-free films can be obtained by highly diluting the monomer in oxygen, while medium-to-high power is necessary to abate silanol groups. These two conditions represent the optimization criterion to obtain excellent barrier films for food packaging applications. 相似文献
995.
Annovazzi L Cattaneo V Viglio S Perani E Zanone C Rota C Pecora F Cetta G Silvestri M Iadarola P 《Electrophoresis》2004,25(9):1255-1263
Tobacco smoke is involved in the pathogenesis of cardiovascular and respiratory diseases and also has a local toxic effect in the oral cavity. Low-aliphatic aldehydes, such as formaldehyde, acetaldehyde and acrolein, are among the main components of mainstream cigarette smoke and their local noxious and carcinogenic effects in the oral cavity and upper gastrointestinal tract are well-known. Although various studies have been performed so far to determine their content in cigarette smoke, none has included the direct measurement of these compounds in the saliva of smoking and nonsmoking subjects. Thus, in an attempt to verify whether typical chromatographic (high-performance liquid chromatography, HPLC) and/or electrophoretic (capillary electrophoresis, CE) techniques could be reliable methods for determining the levels of these analytes in human saliva, we submitted specimens obtained from a selected population of heavy, moderate, and nonsmoking subjects to HPLC and CE analyses. Both methods showed good reproducibility in terms of migration times and peak height and/or areas and had comparable linearity. Quantitative analyses performed on the specimens investigated evidenced a 3.5-fold increase of low-aliphatic aldehydes in saliva of nonsmoking subjects after they have smoked a single cigarette and a further 2-fold increase of these compounds in saliva of smokers with a daily consumption of 10 or more cigarettes. 相似文献
996.
Attanasi OA de Crescentini L Favi G Filippone P Mantellini F Santeusanio S 《The Journal of organic chemistry》2002,67(23):8178-8181
The synthesis of 5-hydroxy-1-aminopyrroline-3-carboxylic acid derivatives and 5-unsubstituted-1-aminopyrrole-3-carboxylic acid derivatives from 1,2-diaza-1,3-butadienes and aldehydes is presented. These domino reactions offer the advantage of executing multistep transformation without intermediate workup procedures. The stereoselectivity of ring closure to 5-hydroxy-1-aminopyrroline-3-carboxylic acid derivatives and phenyl transposition to 2,3-diphenyl-1-aminopyrrole-3-carboxylic acid derivatives are also studied. 相似文献
997.
Fabio Mazzotti Leonardo Di Donna Mohamed Attya Bartolo Gabriele Alessia Fazio Giovanni Sindona 《Rapid communications in mass spectrometry : RCM》2009,23(23):3803-3806
A new approach for the assay of rotenone (1) by isotope dilution mass spectrometry is presented. The extreme toxicity of rotenone, a natural phytodrug with insecticidal and piscicidal activity, recently banned by national and international environmental protection agencies, calls for the development of sensitive and accurate methods of analyses. Accordingly, the proposed protocol is based on the availability of the labeled internal standard rotenone‐d3 (3) which can be conveniently prepared by consecutive and specific mono‐O‐demethylation, and remethylation with methyl iodide‐d3. The sensitivity of the method is confirmed by the very low limit of detection (LOD) and quantitation (LOQ) values achieved in the assay of 1 in two distinct fortified matrices, and is further supported by the observed accuracy values. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
998.
Gaetano Iaquinta Fabio Lamantia Ivar Massabò Sergio Ortobelli 《Annals of Operations Research》2009,165(1):97-121
In this paper we describe and apply the estimating function methodology to value the risk of asset derivative portfolios.
We first implement the Li’s model based on the first four moments and then we show the limits of this model in forecasting
the maximum loss of contingent claims. In addition, we show that four moments are not enough to describe the behavior of the
lower percentiles of derivatives. Finally, we propose a model that considers the first six moments and we compare the performances
of these models proposing a backtest analysis on several historical and truncated asset derivative portfolios. 相似文献
999.
Laura Orsatti Federica Innocenti Paola Lo Surdo Fabio Talamo Gaetano Barbato 《Rapid communications in mass spectrometry : RCM》2009,23(17):2733-2740
The Phosphatase of Regenerating Liver‐3 (PRL‐3) is a cysteine‐based phosphatase (CBP) that is highly over‐expressed in liver metastasis in colorectal cancer and suspected to be involved in the progression from tumor to metastasis. During substrate‐specificity studies based on the screening of PRL‐3 phosphatase activity on several phosphorylated synthetic peptides, we observed a decrease in activity depending on sample aging and storage conditions. By liquid chromatography combined with selective alkylation and mass spectrometry, we found two main PRL‐3 inactivation pathways: a disulfide bond formation between the catalytic C104 and C49, blocking the enzyme in an inactive oxidized form, or the conversion of the catalytic C104 into glycine. We also found that the disulfide formation and the cysteine into glycine conversion are catalyzed by cations present in the sample after protein purification through a nickel column. By adding a cation chelator such as EDTA and de‐oxygenating the sample with argon, PRL‐3 phosphatase activity was preserved. These findings suggest that PRL‐3, like other CBPs, is sensitive to inactivation by catalytic cysteine oxidation and this has implications for future studies of its activity and specificity. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
1000.
Jos Walkimar de M. Carneiro Ceciliana da S. B. de Oliveira Fabio B. Passos Donato A. G. Aranda Paulo Rogrio N. de Souza Octvio A. C. Antunes 《Journal of molecular catalysis. A, Chemical》2001,170(1-2)
The interaction between cinchonidine and methyl pyruvate has been proposed as the key step leading to enantiodifferentiation in the enantioselective hydrogenation of α-ketoesters. In the present work, we employ ab initio MP2/6-31G(d) and MP2/6-31G(d,p) methods to carry out an analysis of the most relevant kind of interactions operating in representative model systems. These interactions are discussed in terms of orbital superposition and dipolar interaction. When approaching H2CO to NH3 at distances lower than 3.4 Å, orbital superposition is the predominant interaction, while at distances above 3.4 Å, both orbital superposition and dipolar interactions may contribute to stabilization, with a small prevalence of dipolar interactions. The stabilization energy at large distances (above 4.5 Å) is very small (about 0.5 kcal mol−1), probably not enough to be responsible for the enantiodifferentiation process. Semiempirical calculations on the parent systems were also unable to reveal any special interaction which could be attributed to the enantiodifferentiation process. 相似文献