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151.
Dissolved organic matter is an important component of the global carbon cycle that allows the distribution of carbon and nutrients. Therefore, analysis of soil dissolved organic matter helps us to better understand climate change impacts as it is the most dynamic and reactive fraction in terrestrial ecosystems. Its characterization at the molecular level is still challenging due to complex mixtures of hundreds of compounds at low concentration levels in percolating water. This work presents simple methods, such as thermochemolysis– or derivatization–gas chromatography, as an alternative for the analysis of fatty acids in dissolved organic matter without any purification step. The variables of the protocols were examined to optimize the processing conditions for the C9–C18 range. As a proof of concept, fatty acid distributions of soil percolating water samples from a long-term field experiment were successfully assessed. The variability of dissolved organic acid distributions was pronounced through depth profile and soil treatment but no major change in composition was observed. However, although the optimization was done from C9 to C18, detection within the C6-C32 fatty acids range was performed for all samples. 相似文献
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Claude Tournut 《Macromolecular Symposia》1994,82(1):99-109
After a brief presentation of the standard non-functionalized copolymers of vinylidene fluoride, the preparation of new functionalized copolymers is described, by copolymerization of vinylidene fluoride, with other fluoromonomers and non-fluorinated monomers including at least one hydroxy or other functional group. The copolymers are analysed by the conventional methods. Examples of formulation show that these new copolymers are able to give coatings applicable outdoors and offering the same excellent durability as PVDF. 相似文献
154.
Giménez-Romero D Agrisuelas J García-Jareño JJ Gregori J Gabrielli C Perrot H Vicente F 《Journal of the American Chemical Society》2007,129(22):7121-7126
This paper demonstrates the importance of the structural changeover in controlling the physical-chemical properties of hexacyanometalate-like materials (Prussian Blue). A meticulous in situ study of compositional variations using electroacoustic impedance techniques associated to electrogravimetric techniques in hexacyanoferrates containing K+ alkali metals reveals the existence of a nanostructural changeover coupled to a change of the magnetic properties of these electromagnetic materials. In the same way, the electroacoustic impedance techniques can be useful both in the understanding and in the in situ monitoring of the structural changeovers and the magnetic behavior of all kinds of materials. 相似文献
155.
Adrián Schwarzenberg Farid Ichou Richard B. Cole Xavier Machuron‐Mandard Christophe Junot Denis Lesage Jean‐Claude Tabet 《Journal of mass spectrometry : JMS》2013,48(5):576-586
Organophosphorus compounds have played important roles as pesticides, chemical warfare agents and extractors of radioactive material. Structural elucidation of phosphonates poses a particular challenge because their initial forms can be hydrolyzed, thus, degradation products may predominate in samples acquired in the field. The analysis of non‐volatile organophosphorus compounds and their degradation products is possible using electrospray tandem mass spectrometry ESI‐MS/MS. Here, we present a generic strategy that allows the unambiguous identification of substituents for two families of organophosphorus compounds: the phosphonates and phosphates. General fragmentation rules were deduced based on the study of decomposition pathways of 55 organophosphorus esters, including examples found in the literature. Multistage MS (MSn) experiments at high resolution in a hybrid mass spectrometer provide accurate mass measurements, whereas collision‐induced dissociation experiments in a triple quadrupole give access to small fragment ions. The creation of a specific nomenclature for each possible structure of organophosphorus compound, depending on the alkyl side chain linked to the oxygen, was achieved by applying these fragmentation rules. This led to the creation of an ‘identification tree’ based upon the unique consecutive decomposition pathways uncovered for each individual compound. Hence, seven structural motifs were created that orient an unequivocal identification using the ‘identification tree’. Despite the similar structures of the ensemble of phosphate and phosphonate esters, distinct identifications based upon characteristic neutral losses and diagnostic fragment ions were possible in all cases. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
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La bande infrarouge v 4 ±1 + v 6 ?1 de CH3 35Cl, centrée vers 4051 cm-1, a été analysée sur un spectre de 0,0075 cm-1 de résolution. On a mis en évidence une résonance l vibrationnelle de couplage R = -2,5 cm-1, et une résonance anharmonique de couplage W F ~4,86 cm-1 avec la bande 4v 6 0 centrée vers 4049 cm-1; par suite de la proximité des deux centres de bande, cette résonance est forte et fait apparaître la sous-bande K = 0 de 4v 6 0. Un calcul de moindres carrés sur 813 raies a donné un écart standard de 0,020 cm-1, de petites anomalies rotationnelles restant à élucider. 相似文献
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