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781.
Riss PJ Lu S Telu S Aigbirhio FI Pike VW 《Angewandte Chemie (International ed. in English)》2012,51(11):2698-2702
Rapid and direct: the carboxylation of boronic acid esters with (11)CO(2) provides [(11)C]carboxylic acids as a convenient entry into [(11)C]esters and [(11)C]amides. This conversion of boronates is tolerant to diverse functional groups (e.g., halo, nitro, or carbonyl). 相似文献
782.
J.D. BadiaE. Strömberg S. Karlsson A. Ribes-Greus 《Polymer Degradation and Stability》2012,97(1):98-107
The action of thermo-mechanical degradation induced by mechanical recycling of poly(ethylene terephthalate) was simulated by successive injection moulding cycles. Degradation reactions provoked chain scissions and a reduction in molar mass mainly driven by the reduction of diethyleneglycol to ethylene glycol units in the flexible domain of the PET backbone, and the formation of -OH terminated species with shorter chain length. The consequent microstructural changes were quantified taking into account a three-fraction model involving crystalline, mobile amorphous (MAF) and rigid amorphous fractions (RAF). A remarkable increase of RAF, to a detriment of MAF was observed, while the percentage of crystalline fraction remained nearly constant. A deeper analysis of the melting behaviour, the segmental dynamics around the glass-rubber relaxation, and the macroscopic mechanical performance, showed the role of each fraction leading to a loss of thermal, viscoelastic and mechanical features, particularly remarkable after the first processing cycle. 相似文献
783.
The triphenylamine-based chemosensors 1 and 2 have been designed and synthesized, for the first time, for the selective recognition of dicarboxylic acids. Carboxylic acid binding takes place through charge neutral pyridyl amide receptor sites with concomitant quenching of fluorescence of the triphenylamine moiety. The bindings were examined using 1H NMR, fluorescence and UV-vis spectroscopic methods. The receptor 1 was found to be selective for glutaric and adipic acids and the macrocycle 2 was specific for 2,2-dimethylmalonic acid. 相似文献
784.
Yongjun Gao Haofan Wang Ronnie C. Mease Martin G. Pomper Andrew G. Horti 《Tetrahedron letters》2010,51(40):5333-5335
Improved syntheses of 7-methyl-2-exo-[3′-(2-bromopyridin-3-yl)-5′-pyridinyl]-7-azabicyclo[2.2.1]heptanes (3) and 7-methyl-2-exo-[3’-(6-bromopyridin-2-yl)-5′-pyridinyl]-7-azabicyclo[2.2.1]heptanes (4), precursors for PET radioligands [18F]XTRA (1) and [18F]AZAN (2), involving a key Stille coupling step followed by deprotection of Boc group and N-methylation are described. The new synthetic procedures provided the title compounds in more than 40% overall yields. 相似文献
785.
Eric D. Morrison Megan W. Malvey Richard D. Johnson Jeffrey S. Hutchison 《Polymer Degradation and Stability》2010,95(4):656-665
A recently described bottle test method was used to evaluate the dependence of stress crack failure of poly(ethylene terephthalate) (PET) carbonated soft drink bottles on water hardness. Although the industry belief is that water hardness is irrelevant to stress cracking, it was found that hardness ions exert a tremendous positive impact by deactivating water alkalinity through precipitation as harmless carbonate minerals. This mitigating effect of hardness means that no complete understanding of stress cracking as a function of alkalinity is possible without also considering water hardness. A useful concept is that of excess alkalinity, which is defined as alkalinity that is not precipitated during solution evaporation. Limiting excess alkalinity by using water with sufficient hardness is an effective means of stress crack prevention in PET soft drink bottles. Evaluation of compositions which are typical of those used for lubricating PET bottles on production conveyors showed that the role of these compositions in stress cracking was that of spectators, that is, they neither cause failure if water does not otherwise cause it, nor stop failure if water otherwise causes it. 相似文献
786.
α-Zr phosphate (hereafter referred to as ZrP) based composites were prepared by melt blending in order to improve the flame retardancy properties of polyamide 6 (PA6), polyethylene terephthalate (PET), polypropylene (PP) and ethylene vinyl acetate copolymer (EVA). Different morphologies are distinguishable by electron microscopy: PA6-ZrP seems to be a nanocomposite by Transmission Electron Microscopy (TEM) whereas PET-, PP- and EVA-ZrP blends appear micro-composites by X-Ray Diffraction (XRD) and Scanning Electron Microscopy (SEM) analyses. ZrP acts as flame retardant in PA6 reducing the total heat evolved and consequently the heat release rate during the combustion measured by cone calorimetry. Moreover, ZrP reduces the flammability of PET and EVA acting in synergistic effect with phosphorous based flame retardants. Indeed, it is showed that it is possible to reduce the amount of phosphorous flame retardant adding ZrP to reach UL94 classification V0 for both polymers. 相似文献
787.
788.
789.
Chemical reactions between poly (vinyl pyridine)s and 1, 4-butanediol diglycidyl ether and other epoxy compounds were studied by Fourier transform infrared spectroscopy and other techniques. The epoxy group was found to react with the pyridine side group of poly (4-vinyl pyridine), forming crosslinked networks which contain cyclic amide structures. The reaction was also observed in the interracial region of poly(vinyl pyridine) and γ-glycidoxy propyl trimethoxysilane hydrolyzate (γ-GPS) coatings on PET fiber substrates. Poly(2-vinyi pyridine) does not show the same reaction. 相似文献
790.
Synthesis of O-(2-[~(18)F]fluoroethyl)-L-tyrosine and its biological evaluation in B16 melanoma-bearing mice as PET tracer for tumor imaging 总被引:1,自引:0,他引:1
O-(2-[18F]fluoroethyl) -L-tyrosine([18F]FET) ,a fluorine-18 labeled analogue of tyrosine,has been syn-thesized and biologically evaluated in tumor-bearing mice. The whole synthesis procedure is com-pleted within 50 min. The radiochemical yield is about 40%(no decay corrected) and radiochemical purity more than 97% after simplified solid phase extraction. [18F]FET shows rapid,high uptake and long retention in the tumor as well as low uptake in the brain. The ratios of tumor-to-muscle(T/M) and tumor-to-blood(T/B) of [18F]FET are similar to those of [18F]FDG,but the ratios of tumor-to-brain(T/Br) are 2-3 times higher than that of [18F]FDG. Autoradiography of [18F]FET demonstrates a remarkable accumulation in melanoma with high contrast. It appears to be a probable competitive candidate for melanoma imaging with PET. 相似文献