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181.
182.
Transmetalated derivatives of bacteriochlorophyll are promising sensitizers in photodynamic therapy. Protocols using short delay times between injection and irradiation cause interest in the photochemistry of these pigments in the blood. Using near-infrared irradiation where these pigments absorb strongly, we have studied the photochemistry of Zn- and Pd-bacteriopheophorbide (WST09), and of the highly polar taurinated Pd-derivative, WST11, in isolated fractions of human blood plasma. The stability of all pigments is increased in blood plasma, compared with monomeric solutions. Pd-bacteriopheophorbide is much more stable than the other two derivatives. It also has a higher capacity for inducing reactive oxygen species, yet the consumption of oxygen is comparable. There is furthermore evidence for photobleaching under anoxic conditions. The generation of hydroperoxides (ROOH) is faster with Pd- than with Zn-complexes; the formation of endoperoxides (ROOR′), measured as thiobarbituric acid reactive substances, is comparable with the two central metals. Formation of both ROOH and ROOR′ is increased in low-density lipoproteins (LDL) compared with high-density lipoproteins (HDL), which is probably related to the higher concentration of target molecules in the former. In HDL, extensive cross-linking is induced among the apolipoproteins; judged from the electrophoretic mobility of LDL and HDL particles, there is also a gross structural change. Photosensitized cross-linking is much less pronounced with high-density proteins. 相似文献
183.
Melissa M. Cadelis Hugo Gordon Alex Grey Soeren Geese Daniel R. Mulholland Bevan S. Weir Brent R. Copp Siouxsie Wiles 《Molecules (Basel, Switzerland)》2021,26(11)
Fungi have become an invaluable source of bioactive natural products, with more than 5 million species of fungi spanning the globe. Fractionation of crude extract of Neodidymelliopsis sp., led to the isolation of a novel polyketide, (2Z)-cillifuranone (1) and five previously reported natural products, (2E)-cillifuranone (2), taiwapyrone (3), xylariolide D (4), pachybasin (5), and N-(5-hydroxypentyl)acetamide (6). It was discovered that (2Z)-cillifuranone (1) was particularly sensitive to ambient temperature and light resulting in isomerisation to (2E)-cillifuranone (2). Structure elucidation of all the natural products were conducted by NMR spectroscopic techniques. The antimicrobial activity of 2, 3, and 5 were evaluated against a variety of bacterial and fungal pathogens. A sodium [1-13C] acetate labelling study was conducted on Neodidymelliopsis sp. and confirmed that pachybasin is biosynthesised through the acetate polyketide pathway. 相似文献
184.
185.
The influence of macro-scale heterogeneities on the imbibition process is investigated for Savonnières, a French layered limestone. Free uptake experiments are performed both parallel and perpendicular to the bedding. It is found that the position of the different layers, and the exact material properties inside each layer can significantly influence the imbibition process. The experimental results are compared with numerical simulations. For the flow simulations, moisture permeability of the different layers is obtained with the upscaling technique presented in Part 1. Good agreement between simulations and experiments validate the proposed upscaling from meso to macroscopic scale. 相似文献
186.
187.
Hugo Sinnhold 《Fresenius' Journal of Analytical Chemistry》1901,40(6):407
Ohne Zusammenfassung 相似文献
188.
189.
Hugo Ludwig Fulda 《Monatshefte für Chemie / Chemical Monthly》1901,20(8):698-716
Ohne Zusammenfassung 相似文献
190.
María E. Noble-Terán Dr. José-Manuel Cruz Dr. Hugo I. Cruz-Rosas Dr. Thomas Buhse Dr. Jean-Claude Micheau 《Chemphyschem》2023,24(18):e202300318
Attrition-enhanced chiral symmetry breaking in crystals, known as Viedma deracemization, is a promising method for converting racemic solid phases into enantiomerically pure ones under non-equilibrium conditions. However, many aspects of this process remain unclear. In this study, we present a new investigation into Viedma deracemization using a comprehensive kinetic rate equation continuous model based on classical primary nucleation theory, crystal growth, and Ostwald ripening. Our approach employs a fully microreversible kinetic scheme with a size-dependent solubility following the Gibbs–Thomson rule. To validate our model, we use data from a real NaClO3 deracemization experiment. After parametrization, the model shows spontaneous mirror symmetry breaking (SMSB) under grinding. Additionally, we identify a bifurcation scenario with a lower and upper limit of the grinding intensity that leads to deracemization, including a minimum deracemization time within this window. Furthermore, this model uncovers that SMSB is caused by multiple instances of concealed high-order autocatalysis. Our findings provide new insights into attrition-enhanced deracemization and its potential applications in chiral molecule synthesis and understanding biological homochirality. 相似文献