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91.
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93.
Yukun Cheng Xiaotie Deng Dominik Scheder 《4OR: A Quarterly Journal of Operations Research》2018,16(3):231-260
Market makers choose and design market rules to serve certain objectives, such as to maximize revenue from the sales in the case of a single seller and multiple buyers. Given such rules, market participants play against each other to maximize their utility function values on goods acquired, possibly by hiding or misrepresenting their information needed in the implementation of market rules. Today’s Internet economy has changed the information collection process and may make some of the assumptions of market rule implementation obsolete. Here we make a fresh review of works on this challenge on the Internet where new economic systems operate. 相似文献
94.
Dominik Dorsch Hubertus Th. Jongen Vladimir Shikhman 《Set-Valued and Variational Analysis》2011,19(2):237-253
We examine the topological structure of the upper-level set M max given by a min-max function φ. It is motivated by recent progress in Generalized Semi-Infinite Programming (GSIP). Generically, M max is proven to be the topological closure of the GSIP feasible set (see Guerra-Vázquez et al. 2009; Günzel et al., Cent Eur J Oper Res 15(3):271–280, 2007). We formulate two assumptions (Compactness Condition CC and Sym-MFCQ) which imply that M max is a Lipschitz manifold (with boundary). The Compactness Condition is shown to be stable under C 0-perturbations of the defining functions of φ. Sym-MFCQ can be seen as a constraint qualification in terms of Clarke’s subdifferential of the min-max function φ. Moreover, Sym-MFCQ is proven to be generic and stable under C 1-perturbations of the defining functions which fulfill the Compactness Condition. Finally we apply our results to GSIP and conclude that generically the closure of the GSIP feasible set is a Lipschitz manifold (with boundary). 相似文献
95.
Raphaël Robidas Dominik L. Reinhard Prof. Stefan M. Huber Prof. Claude Y. Legault 《Chemphyschem》2023,24(1):e202200634
Cyclic diaryliodonium compounds like iodolium derivatives have increasingly found use as noncovalent Lewis acids in the last years. They are more stable toward nucleophilic substitution than acyclic systems and are markedly more Lewis acidic. Herein, this higher Lewis acidity is analyzed and explained via quantum-chemical calculations and energy decomposition analyses. Its key origin is the change in energy levels and hybridization of iodine's orbitals, leading to both more favorable electrostatic interaction and better charge transfer. Both of the latter seem to contribute in similar fashion, while hydrogen bonding as well as steric repulsion with the phenyl rings play at best a minor role. In comparison to iodolium, bromolium and chlorolium are less Lewis acidic the lighter the halogen, which is predominantly based on less favorable charge-transfer interactions. 相似文献
96.
Dr. Jan Lorkowski Dylan Bouetard Patrick Yorkgitis Dr. Milan Gembicky Dr. Thierry Roisnel Dr. Nicolas Vanthuyne Prof. Dr. Dominik Munz Dr. Ludovic Favereau Prof. Dr. Guy Bertrand Dr. Marc Mauduit Dr. Rodolphe Jazzar 《Angewandte Chemie (International ed. in English)》2023,62(33):e202305404
Organic circularly polarized luminescence (CPL)-active molecular emitters featuring dynamic propeller-like luminophores were prepared in one step from cyclic(alkyl)(amino) carbenes (CAACs). These molecules exhibit through-space arene-arene π-delocalization and rapid intramolecular inter-system crossing (ISC) in line with their helical character. 相似文献
97.
Generating realistic vehicle speed trajectories is a crucial component in evaluating vehicle fuel economy and in predictive control of self-driving cars. Traditional generative models rely on Markov chain methods and can produce accurate synthetic trajectories but are subject to the curse of dimensionality. They do not allow to include conditional input variables into the generation process. In this paper, we show how extensions to deep generative models allow accurate and scalable generation. Proposed architectures involve recurrent and feed-forward layers and are trained using adversarial techniques. Our models are shown to perform well on generating vehicle trajectories using a model trained on GPS data from Chicago metropolitan area. 相似文献
98.
W. Ryba-Romanowski S. Go
b G. Dominiak-Dzik W. A. Pisarski D. Podsiada Z. Czapla 《Journal of Molecular Structure》1998,450(1-3):219-222
Chromium doped (CH3)2NH2Al(SO4)2·6H2O (DMAAlS) and (CH3)2NH2Ga(SO4)2·6H2O (DMAGaS) single crystals were grown and investigated using the methods of optical spectroscopy. It was found that the Cr3+ ions in the two crystals are situated in a strong crystal field in which the 2E state is the lowest. The single narrow R-line associated with the 2E–4A2 phosphorescence of Cr3+ in DMAAlS in a ferroelectric phase indicates an undistorted octahedral site, whereas important distortion of Oh symmetry and structural disorder was inferred from spectral data obtained with DMAGaS:Cr3+ in a low temperature phase. Results of optical investigation are discussed taking into account the structural data. 相似文献
99.
Hsieh HT Psaltis D Beyer O Maxein D von Korff Schmising C Buse K Sturman B 《Optics letters》2005,30(17):2233-2235
Spatial gratings are recorded holographically by two femtosecond pump pulses at 388 nm in lithium niobate (LiNbO3) crystals and read out by a Bragg-matched, temporally delayed probe pulse at 776 nm. We claim, to our knowledge, the first holographic pump-probe experiments with subpicosecond temporal resolution for LiNbO3. An instantaneous grating that is due mostly to the Kerr effect as well as a long-lasting grating that results mainly from the absorption caused by photoexcited carriers was observed. The Kerr coefficient of LiNbO3 for our experimental conditions, i.e., pumped and probed at different wavelengths, was approximately 1.0 x 10(-5) cm2/GW. 相似文献
100.
Annekathrin Seifert Dominik Scheid Gerald Linti Prof. Dr. Thomas Zessin 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(44):12114-12120
The gallium(I) derivative [Ga({N(dipp)CMe}2CH)] ( 1 ; dipp=2,6‐diisopropylphenyl) undergoes facile oxidative addition reactions with various element–hydrogen bonds including N? H, P? H, O? H, Sn? H, and H? H bonds. This was demonstrated by its reaction with triphenyltin hydride, ethanol, water, diethylamine, diphenylphosphane, and dihydrogen. All products were characterized by means of single‐crystal X‐ray structure determination, NMR spectroscopy, IR spectroscopy, and mass spectrometry. 相似文献