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91.
92.
Let Ω be a bounded domain of the complex plane whose boundary is a closed Jordan curve and (F
n
)
n≥0 the sequence of Faber polynomials of Ω. We say that a bounded linear operator T on a separable Banach space X is Ω-hypercyclic if there exists a vector x of X such that {F
n
(T)x: n ≥ 0} is dense in X. We show that many of the results in the spectral theory of hypercyclic operators involving the unit disk or its boundary
have Ω-hypercyclic counterparts which involve the domain Ω or its boundary. The influence of the geometry of Ω or the smoothness
of its boundary on Faber-hypercyclicity is also discussed. 相似文献
93.
Alexander Alex Sophie Harvey Teresa Parsons Frank S. Pullen Patricia Wright Jo‐Anne Riley 《Rapid communications in mass spectrometry : RCM》2009,23(17):2619-2627
Prediction of tandem mass spectrometric (MS/MS) fragmentation for non‐peptidic molecules based on structure is of immense interest to the mass spectrometrist. If a reliable approach to MS/MS prediction could be achieved its impact within the pharmaceutical industry could be immense. Many publications have stressed that the fragmentation of a molecular ion or protonated molecule is a complex process that depends on many parameters, making prediction difficult. Commercial prediction software relies on a collection of general heuristic rules of fragmentation, which involve cleaving every bond in the structure to produce a list of ‘expected’ masses which can be compared with the experimental data. These approaches do not take into account the thermodynamic or molecular orbital effects that impact on the molecule at the point of protonation which could influence the potential sites of bond cleavage based on the structural motif. A series of compounds have been studied by examining the experimentally derived high‐resolution MS/MS data and comparing it with the in silico modelling of the neutral and protonated structures. The effect that protonation at specific sites can have on the bond lengths has also been determined. We have calculated the thermodynamically most stable protonated species and have observed how that information can help predict the cleavage site for that ion. The data have shown that this use of in silico techniques could be a possible way to predict MS/MS spectra. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
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96.
Alan R. Katritzky Nabin K. Meher Sureyya Hanci Reena Gyanda Srinivasa R. Tala Sindhu Mathai Randolph S. Duran Sophie Bernard Firouzeh Sabri Sandeep K. Singh Jacek Doskocz David A. Ciaramitaro 《Journal of polymer science. Part A, Polymer chemistry》2008,46(1):238-256
Fourteen commercial polyols have been characterized by GPC, NMR spectroscopy, and elemental analysis. From these, eight corresponding tosylates, six nitrate esters, seven mesylates, 13 alkynes, and 14 azides have been prepared and all these derivatives have been fully characterized. Five alkyne monomers and eight azide monomers were also prepared. Twelve alkynes and 13 azides (functionality 2–4) were combined in 1,3‐dipolar cycloaddition reactions under neat conditions to prepare triazole‐cured polymers, avoiding any heavy metal catalyst. Characterization by NMR spectroscopy, elemental analysis, and gel permeation chromatography indicated triazole polymers 14 , 22 , 23 , 28 , and 30 with degrees of polymerization of 17–28 to be the best candidates for future work. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 238–256, 2008 相似文献
97.
Sophie J. Ssinjakova 《Fresenius' Journal of Analytical Chemistry》1935,100(5-6):190-193
Zusammenfassung Es wird ein nephelometrisches Verfahren beschrieben, bei dem Strychnin und Jodid zur Anwendung gelangen. Dieses Verfahren ist genügend exakt und bequem und eignet sich für die Bestimmung von Quecksilber in Mengen bis zu 2 y.Die Arbeit wurde unter der Leitung von Professor A. V. Pamfilov ausgeführt. 相似文献
98.
Sophie Bourcier Yannik Hoppilliard 《Rapid communications in mass spectrometry : RCM》2009,23(1):93-103
This work presents the use of neutral losses (NL) for the identification of compounds related to the metabolism of tyrosine. The mass spectra of all the studied compounds, recorded at several collision energies, are compared. The fragmentation mechanism of protonated molecules, MH+, is explained by combining collision‐induced dissociation (CID) mass spectra and density functional theory (DFT) calculations. The results show that the first fragmentation is the elimination from MH+ of a neutral molecule including a functional group of the linear chain. Three primary neutral losses are observed: 17 u (NH3), 18 u (H2O) and 46 u (H2O+CO) characterizing amino, hydroxyl and carboxylic functions on the linear chain. The presence and abundance of ions corresponding to these losses are dependent on (i) the position of the functional group on the linear chain, (ii) the initial localisation of the protonating hydrogen, and (iii) the substitution of the aromatic ring. For compounds including a functional group on the benzylic carbon atom, the investigation of the other functions requires the knowledge of secondary fragmentations. Among these secondary fragmentations we have retained the loss of NH3 from [MH–18u]+ and the loss of ketene from [MH–17u]+. Experimentally these fragmentations are detected using losses of 35 u and 59/73 u. In other words, NL35 identifies hydroxy and amino compounds and NL 46 and/or NL59/73 identify carboxylic acids. The search for characteristic neutral losses is used for the analysis of compounds in a mixture and the analysis of biological fluid. We show that selective search of several neutral losses allows also the unambiguous differentiation of isomers and gives the opportunity to identify compounds in biological fluids. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
99.
Ohne Zusammenfassung 相似文献
100.