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991.
992.
Kensuke MiyazakiKazuto Shibata Hisayuki Nakatani 《Polymer Degradation and Stability》2011,96(5):1039-1046
In this work, biodegradation behavior of a novel polypropylene (PP) composite containing a poly(ethylene oxide) (PEO)/modified TiO2 microcapsule was studied with an oxo-biodegradation test combined with a photodegradation treatment (using a high-pressure mercury vapor lamp for 24 h of the irradiation at 30 °C in air) and a soil burial test (for 45 days of incubation at 20 °C). The modification of the TiO2 was performed by the synthesis of octacalcium phosphate intercalated with succinic acid ion (OCPC). The existence of the microcapsule brought about higher PP photo- and biodegradation rates. In the photodegraded PP composite, active colonies of some microorganisms were observed. By comparing with the PP composite without the OCPC modification, it was found that the active behavior of the microorganisms was due to the inorganic phosphates, which were supplied by the dissolution of the OCPC during the photodegradation. In addition, the photodegraded parts in the composite were completely metabolized by the microorganisms. However, the microorganisms had the inability to metabolize other parts such as the PP crystalline phase. 相似文献
993.
994.
Hiranita T Nakamura S Kawachi M Courrier HM Vandamme TF Krafft MP Shibata O 《Journal of colloid and interface science》2003,265(1):83-92
Surface pressure-area, surface potential-area, and dipole moment-area isotherms were obtained for monolayers made from a partially fluorinated surfactant, (perfluorooctyl)undecyldimorpholinophosphate (F8H11DMP), dipalmitoylphosphatidylcholine (DPPC), and their combinations. Monolayers, spread on a 0.15 M NaCl subphase, were investigated at the air/water interface by the Wilhelmy method, ionizing electrode method, and fluorescence microscopy. Surface potentials were analyzed using the three-layer model proposed by Demchak and Fort. The contribution of the dimorpholinophosphate polar head group of F8H11DMP to the vertical component of the dipole moment was estimated to be 4.99 D. The linear variation of the phase transition pressure as a function of F8H11DMP molar fraction (X(F8H11DMP)) demonstrated that DPPC and F8H11DMP are miscible in the monolayer. This result was confirmed by deviations from the additivity rule observed when plotting the molecular areas and the surface potentials as a function of X(F8H11DMP) over the whole range of surface pressures investigated. Assuming a regular surface mixture, the Joos equation, which was used for the analysis of the collapse pressure of mixed monolayers, allowed calculation of the interaction parameter (xi=-1.3) and the energy of interaction (Delta epsilon =537 Jmol(-1)) between DPPC and F8H11DMP. The miscibility of DPPC and F8H11DMP within the monolayer was also supported by fluorescence microscopy. Examination of the observed flower-like patterns showed that F8H11DMP favors dissolution of the ordered LC phase domains of DPPC, a feature that may be key to the use of phospholipid preparations as lung surfactants. 相似文献
995.
Analytical methods for the speciation of nine selenium species (selenite, selenate, selenourea, trimethylselenonium ion, selenocystamine, selenocystine, selenocysteine, selenomethionine and selenoethionine) that are commonly encountered in biological and environmental samples were developed. Good separation was achieved by either a mixed ion-pair reversed phase chromatography (LiChrosorb RP 18, 2.5 mM 1-butanesulfonate-8 mM tetramethylammonium hydroxide-4 mM malonic acid-0.05% methanol, pH 4.5) or a conventional ion-pair reversed phase chromatography (Inertsil ODS, 10 mM tetraethylammonium hydroxide-4.5 mM malonic acid, pH 6.8) with on-line ICP-MS detection. Using a 20-μl sample loop, low detection limits around 1 ng ml−1 expressed as Se were achieved for the examined selenium species. The methods were used for the determination of selenoamino acids in a selenium nutritional supplement. The developed methods were found to be rather robust. No alteration of the separation was observed when the protease enzymatic extracts were analyzed without dilution. Both water extracts and enzymatic extracts were chromatographed first with the mixed ion-pair reversed phase chromatographic system, then the major chromatographic peaks were collected and analyzed by the second ion-pair reversed phase chromatographic system for a further verification of their identity. Selenomethionine was found to be the major selenium species in the supplement. A major unknown species, probably Se-adenosylhomocysteine, could be determined in the extracts. A biological reference material, Dolt-2, was also examined for the selenoamino acids. Selenocystine and selenomethionine could be detected in its enzymatic extract, suggesting that Dolt-2 may be used as a reference material for the identification of selenoamino acids in biological and environmental samples. As selenoethionine does not occur naturally in the investigated samples, it is added as an internal standard in this study. 相似文献
996.
A layer-by-layer assembled and molecular-complexed polymer membrane was prepared by the simple combination of poly(4-styrenesulfonic acid) and poly(allylamine) on a comb-shaped gold electrode: it displayed a very high proton conductivity of 10(-3) S cm(-1) under a dry condition at 120 degrees C. 相似文献
997.
A simultaneous micro-determination of nicotinamide and its major metabolites, N1-methyl-2-pyridone-5-carboxamide (2-py) and N1-methyl-4-pyridone-3-carboxamide (4-py) by high-performance liquid chromatography is described. The method employs a 7-ODS-L (250 mm X 4.6 mm I.D., particle size 7 microns) column eluted with 10 mM potassium dihydrogenphosphate-acetonitrile (96:4, v/v; pH adjusted to 3.0 by the addition of concentrated phosphoric acid) at a flow-rate of 1.0 ml/min. The UV detector was set at 260 nm. The detection limits for nicotinamide, 2-py and 4-py were 10 pmol (1.22 ng), 2 pmol (304 pg) and 2 pmol (304 pg), respectively, at a signal-to-noise ratio 5:1. Isonicotinamide was used as an internal standard. The technique was applied to the analysis of rat and human urines. The total analysis time was ca. 15 min. 相似文献
998.
999.
Construction of Quaternary Stereogenic Carbon Centers through Copper‐Catalyzed Enantioselective Allylic Alkylation of Azoles 下载免费PDF全文
Prof. Dr. Hirohisa Ohmiya Heng Zhang Saori Shibata Ayumi Harada Prof. Dr. Masaya Sawamura 《Angewandte Chemie (International ed. in English)》2016,55(15):4777-4780
Copper‐catalyzed enantioselective allylic alkylation of azoles with γ,γ‐disubstituted primary allylic phosphates was achieved using a new chiral N‐heterocyclic carbene ligand bearing a naphtholic hydroxy group. This reaction occurred with excellent branch regioselectivity and high enantioselectivity, thus forming a controlled all‐carbon quaternary stereogenic center at the position α to the heteroaromatic ring. 相似文献
1000.