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41.
Christian K. Frese Dirk Nolting A. F. Maarten Altelaar Jens Griep-Raming Shabaz Mohammed Albert J. R. Heck 《Journal of the American Society for Mass Spectrometry》2013,24(11):1663-1670
Electron transfer dissociation (ETD) is commonly employed in ion traps utilizing rf fields that facilitate efficient electron transfer reactions. Here, we explore performing ETD in the HCD collision cell on an Orbitrap Velos instrument by applying a static DC gradient axially to the rods. This gradient enables simultaneous three dimensional, charge sign independent, trapping of cations and anions, initiating electron transfer reactions in the center of the HCD cell where oppositely charged ions clouds overlap. Here, we evaluate this mode of operation for a number of tryptic peptide populations and the top-down sequence analysis of ubiquitin. Our preliminary data show that performing ETD in the HCD cell provides similar fragmentation as ion trap-ETD but requires further optimization to match performance of ion trap-ETD. 相似文献
42.
Ugo Bussy Illa Tea Véronique Ferchaud-Roucher Michel Krempf Virginie Silvestre Nicolas Galland Denis Jacquemin Moa Andresen-Bergström Ulrik Jurva Mohammed Boujtita 《Analytica chimica acta》2013
The coupling between an electrochemical cell (EC) and a mass spectrometer (MS) is a useful screening tool (EC-MS) to study the oxidative transformation pathways of various electroactive species. For that purpose, we showed that the EC-MS method, carried out in the presence and absence of isotope 18O labeled water leads not only to a fast identification of oxidation products but also leads to a fast elucidation of the mechanism pathway reaction. We examined herein the case of the electrochemical hydrolysis of activated aromatic ether. Acebutolol (β-blockers) was selected herein as model of activated aromatic ether, and its electrochemical oxidation was examined in both the presence and absence of isotope 18O labeled water. To elucidate electrochemical hydrolysis pathway reaction: O-dealkylation or O-dealkoxylation, our approach was used to prove its applicability. The electrochemical oxidation mechanism was then elucidated showing an O-dealkoxylation reaction. In addition, density functional theory (DFT) calculations fully support the experimental conclusions. 相似文献
43.
Immunomagnetic nanoparticle based quantitative PCR for rapid detection of Salmonella 总被引:1,自引:0,他引:1
Padmavathy Bakthavathsalam Vinoth Kumar Rajendran Uttara Saran Suvro Chatterjee Baquir Mohammed Jaffar Ali 《Mikrochimica acta》2013,180(13-14):1241-1248
We have developed a rapid and sensitive method for immunomagnetic separation (IMS) of Salmonella along with their real time detection via PCR. Silica-coated magnetic nanoparticles were functionalized with carboxy groups to which anti-Salmonella antibody raised against heat-inactivated whole cells of Salmonella were covalently attached. The immuno-captured target cells were detected in beverages like milk and lemon juice by multiplex PCR and real time PCR with a detection limit of 104 cfu.mL?1 and 103 cfu.mL?1, respectively. We demonstrate that IMS can be used for selective concentration of target bacteria from beverages for subsequent use in PCR detection. PCR also enables differentiation of Salmonella typhi and Salmonella paratyphi A using a set of four specific primers. In addition, IMS—PCR can be used as a screening tool in the food and beverage industry for the detection of Salmonella within 3–4 h which compares favorably to the time of several days that is needed in case of conventional detection based on culture and biochemical methods.
The method uses silica coated magnetic nanoparticles immobilized with anti-Salmonella antibody for immunomagnetic separation of Salmonella from beverages followed by detection by multiplex PCR (mPCR) and real time PCR (qPCR). This methodology contributes to rapid screening and accurate detection of Salmonella contaminations in beverages. 相似文献
44.
4-Aminoperoxybenzoic acid supported on silica gel was found to be a versatile and efficient oxidant for the oxidation of ketones to esters. 相似文献
45.
An efficient synthesis of predominantly (E) symmetrical or unsymmetrical 1,2-difluorostilbenes based on the Suzuki–Miyaura palladium-catalyzed cross-coupling reaction of arylboronic acids with predominantly (E)-1,2-dibromo-1,2-difluoroethene in the presence of Cs2CO3 in toluene is described. The reaction preserved the stereochemistry of the building block and performed in good yield independently of the electron-withdrawing or electron-donating character of the substituents. 相似文献
46.
Formation, crystal structure, polymorphism, and transition between polymorphs are reported for M(thd)3, (M = Al, Cr, Mn, Fe, Co, Ga, and In) [(thd)– = anion of H(thd) = C11H20O2 = 2, 2, 6, 6‐tetramethylheptane‐3, 5‐dione]. Fresh crystal‐structure data are provided for monoclinic polymorphs of Al(thd)3, Ga(thd)3, and In(thd)3. Apart from adjustment of the M–Ok bond length, the structural characteristics of M(thd)3 complexes remain essentially unaffected by change of M. Analysis of the M–Ok, Ok–Ck, and Ck–Ck distances support the notion that the M–Ok–Ck–Ck–Ck–Ok– ring forms a heterocyclic unit with σ and π contributions to the bonds. Tentative assessments according to the bond‐valence or bond‐order scheme suggest that the strengths of the σ bonds are approximately equal for the M–Ok, Ok–Ck, and Ck–Ck bonds, whereas the π component of the M–Ok bonds is small compared with those for the Ok–Ck, and Ck–Ck bonds. The contours of a pattern for the occurrence of M(thd)3 polymorphs suggest that polymorphs with structures of orthorhombic or higher symmetry are favored on crystallization from the vapor phase (viz. sublimation). Monoclinic polymorphs prefer crystallization from solution at temperatures closer to ambient. Each of the M(thd)3 complexes subject to this study exhibits three or more polymorphs (further variants are likely to emerge consequent on systematic exploration of the crystallization conditions). High‐temperature powder X‐ray diffraction shows that the monoclinic polymorphs convert irreversibly to the corresponding rotational disordered orthorhombic variant above some 100–150 °C (depending on M). The orthorhombic variant is in turn transformed into polymorphs of tetragonal and cubic symmetry before entering the molten state. These findings are discussed in light of the current conceptions of rotational disorder in molecular crystals. 相似文献
47.
Ahmed A. K. Mohammed Peter A. Limacher Benoît Champagne 《Journal of computational chemistry》2013,34(17):1497-1507
The finite field method, widely used for the calculation of static dipole polarizabilities or the first and second hyperpolarizabilities of molecules and polymers, is thoroughly explored. The application of different field strengths and the impact on the precision of the calculations were investigated. Borders could be defined and characterized, establishing a range of feasible field strengths that guarantee reliable numerical results. The quality of different types of meshes to screen the feasible region is assessed. Extrapolation schemes are presented that reduce the truncation error and allow to increase the precision of finite field calculations by one to three orders of magnitude. © 2013 Wiley Periodicals, Inc. 相似文献
48.
A.-H. Abdel-Rahman Adel E. El Aassy Ibrahim Y. Ahmed Fadia F. Hamza Mohammed 《Journal of Dispersion Science and Technology》2013,34(8):1128-1135
Synthesis of poly(acrylamidoxime) resin from polyacrylonitrile performed with different crosslinking ratios 2, 5, and 10 wt% of divinylbenzene as crosslinking agent, using methylbenzoate and dioctylphthalate as pore producing solvent, the reaction mixture occurred under nitrogen. Studies carried out on diluted solution from rare earth elements (REEs) concentrate contains impurities as Cu2+, Ni2+, Zn2+, Fe3+, Al3+, Si4+, Th4+, U6+, Ca2+, and K+. Changing some parameters as pH of the solution, time of feeding and type of acid as HCl, HNO3, H2SO4. The adsorption efficiency of resin is in the order pH 6 > pH 5 > pH 4 > pH 2 with excluding pH 6 due to the precipitation of some of REEs with the impurities and complete precipitation of Dy ion during pH adjustment, the adsorption in HNO3 > HCl > H2SO4 media. 相似文献
49.
Mohammed Taghi Zafarani-Moattar Roghayeh Majdan-Cegincara 《Colloid and polymer science》2013,291(8):1977-1987
The Fe3O4 nanoparticles and Fe3O4 nanoparticles coated with oleic acid have been dispersed in base fluid of poly(ethylene glycol) (PEG). Stability and particle size distribution of these nanofluids have been studied by result analysis of UV–Vis spectroscopy, zeta potential and dynamic light scattering. Blue shift of UV–Vis spectra has been related to quantum effects such as band gap enlargement with particle size decreasing and also to effect of oleic acid on the ultraviolet wavelength. Flow behavior and suspension structure of Fe3O4 nanoparticles dispersed in PEG have been determined by rheological properties. Viscosity values of Fe3O4-PEG nanofluid as a function of temperature have also been investigated. The chain-like structure of Fe3O4 nanoparticles coated with oleic acid in base fluid of PEG has been verified by measuring the magnetorheological properties. The effect of temperature on magnetorheological properties of Fe3O4 nanoparticles coated with oleic acid has also been investigated in base fluid of PEG. The volumetric properties of Fe3O4-PEG and Fe3O4 coated with oleic acid–PEG nanofluids and PEG–oleic acid solution have also been measured at different temperatures to specify the suspension structure and also interactions of Fe3O4, PEG and oleic acid molecules. 相似文献
50.
A simple, rapid, sensitive, and inexpensive method for spectrophotometric determination of chromium(VI), based on the absorbance of its complex with 1,4,8,11-tetraazacyclotetradecane (cyclam) is presented. The complex showed a molar absorbtivity of 1.5?×?104?L?mol?1?cm?1 at 379?nm. Under optimum experimental conditions, a pH of 4.5 and 1.960?×?103?mg?L?1 cyclam were selected, and all measurements were performed 10?min after mixing. Major cations and anions did not show any interference; Beer's law was applicable in the concentration range 0.2–20?mg?L?1 with a detection limit of 0.001?mg?L?1. The standard deviation in the determination is ±0.5?mg?L?1 for a 15.0?mg?L?1 solution (n?=?7). The described method provides a simple and reliable means for determination of Cr(VI) in real samples. 相似文献