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排序方式: 共有1197条查询结果,搜索用时 15 毫秒
81.
Nirvik Sen K. Saswani K. K. Singh S. Barkade S. Mukhopadhyay S. M. Chavan Sk. M. Ali K. T. Shenoy 《Journal of Radioanalytical and Nuclear Chemistry》2017,312(2):255-262
Batch extraction of uranium(VI) from uranyl nitrate solutions using TiAP in ionic liquids ([BMIM]PF6 and [HMIM]PF6) is studied. Effects of acidity, TiAP concentration in ionic liquid and temperature on distribution coefficient are studied. Results show that distribution coefficient increases with an increase in acidity and reduces with an increase in the alkyl chain length of the cation of the ionic liquid. Extraction of uranium(VI) by TiAP-[HMIM]PF6 system is found to involve two molecules of the extractant per metal ion and extraction is found to change from being exothermic to endothermic as the percentage of the extractant is increased. 相似文献
82.
A stereoselective synthesis of the C1-C15 fragment of a G-actin binding natural macrodiolide, rhizopodin was achieved using, as key steps, highly stereoselective acetate aldol reactions to build the C1-C7 fragment, one pot oxazole synthesis and an asymmetric Keck allylation reaction to build the C8-C15 fragment and finally, a Stille reaction to couple both the fragments. 相似文献
83.
Sengupta P Sarkar AK Bhaumik U Chatterjee B Roy B Chakraborty US Pal TK 《Biomedical chromatography : BMC》2010,24(12):1342-1349
A simple, high‐throughput and specific high‐performance liquid chromatography tandem mass spectrometry method has been developed and validated according to the FDA guidelines for simultaneous quantification of olmesartan and pioglitazone in rat plasma. The bioanalytical method consists of liquid–liquid extraction and quantitation by triple quadrupole mass spectrometry using electrospray ionization technique, operating in multiple reaction monitoring and positive ion modes. The compounds were eluted isocratically on a C18 column with a mobile phase consisting of a mixture of methanol and water (containing 0.5% formic acid) in a ratio of 9:1. The response to olmesartan and pioglitazone was linear over the range 0.01–10 µg/mL. The validation results demonstrated that the method had satisfactory precision and accuracy across the calibration range. Intra‐ and inter‐day precisions ranged from 0.66 to 3.32 and from 0.94 to 2.93% (%CV), respectively. The accuracy determined at three quality control levels was within 91.27–107.28%. There was no evidence of instability of the analytes in rat plasma following the stability studies. The method proved highly reproducible and sensitive and was successfully applied in a pharmacokinetic study after single dose oral administration of olmesartan and pioglitazone to the rat. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
84.
Mrinal Kanti Paira Tapan Kumar Mondal Elena López-Torres Joan Ribas Chittaranjan Sinha 《Polyhedron》2010
Copper(II) complexes of 3-((2-(alkylthio)phenylazo)-2,4-pentanedione, tridentate O, N, S donor ligands, are described in this work. Chloride bridged copper(II) polymers (1) and thiocyanato bridged copper(II) dimmers (2) are characterized by a single crystal X-ray diffraction study. The complexes show antiferromagnetic interactions, with J = −0.5 ± 0.1 cm−1 (1a) and −25.8 ± 0.5 cm−1 (2b), which implies stronger coupling in the –SCN-bridging compound. The spectra, redox and magnetism are explained by DFT studies. 相似文献
85.
86.
Karmakar S Das O Ghosh S Zangrando E Johann M Rentschler E Weyhermüller T Khanra S Paine TK 《Dalton transactions (Cambridge, England : 2003)》2010,39(45):10920-10927
A new dicompartmental dioxime ligand (H(2)L) with m-xylyl spacer between the donor sites has been synthesised by Schiff-base condensation of α,α'-diamino-m-xylene and diacetyl monooxime. The ligand reacts with copper(ii) salts giving rise to hexanuclear tricationic copper(II) cage complexes [Cu(II)(6)(μ(3)-O···H···O-μ(3))L(3)(H(2)O)(6)]X(3) (X = BF(4), 1a; X = ClO(4), 1b). The complexes have been characterised by different analytical and spectroscopic techniques and confirmed the hexanuclear structure even in solution. Single crystal X-ray diffraction studies of both the complexes revealed a very similar core structure with three dicompartmental ligands supporting two triangular Cu(3)O cores that share a proton, located on their common threefold axis and involved in a strong hydrogen bond interaction (O···O distance of 2.517(2) ?). Two Cu(3)O units do not superimpose but are staggered and disposed with the formation of a helicate structure. However both the enantiomers are present in the centrosymmetric space group. The facing Cu(3)-planes in 1a are separated at a distance of 3.476 ?. The temperature dependence of the magnetic behaviour of the hexanuclear complex 1a clearly indicates an overall antiferromagnetic exchange interaction between the spin carriers in the cage having two Cu(3)O subunits and leaves a single unpaired electron in each triangular unit. The unpaired electrons in the two Cu(3)O units interact antiferromagnetically through hydrogen bonding giving rise to an overall singlet-spin ground state. 相似文献
87.
The study of protein conformational changes in the presence of surfactants and lipids is important in the context of protein
folding and misfolding. In the present study, we have investigated the mechanism of the protein conformational change coupled
with aggregation leading to size growth of Hen Egg White Lysozyme (HEWL) in the presence of an anionic detergent such as sodium
dodecyl sulphate (SDS) in alkaline pH. We have utilized intrinsic protein fluorescence (tryptophan) and extrinsic fluorescent
reporters such as 8-anilinonaphthalene-1-sulfonic acid (ANS), dansyl and fluorescein to follow the protein conformational
change in real-time. By analyzing the kinetics of fluorescence intensity and anisotropy of multiple fluorescent reporters,
we have been able to delineate the mechanism of surfactant-induced aggregation of lysozyme. The kinetic parameters reveal
that aggregation proceeds with an initial fast-phase (conformational change) followed by a slow-phase (self-assembly). Our
results indicate that SDS, below critical micelle concentration, induces conformational expansion that triggers the aggregation
process at a micromolar protein concentration range. 相似文献
88.
Mounce AM Oh S Mukhopadhyay S Halperin WP Reyes AP Kuhns PL Fujita K Ishikado M Uchida S 《Physical review letters》2011,106(5):057003
Competition with magnetism is at the heart of high-temperature superconductivity, most intensely felt near a vortex core. To investigate vortex magnetism we have developed a spatially resolved probe based upon NMR spin-lattice-relaxation spectroscopy. With this approach we have found a spin-density wave associated with the vortex core in Bi(2)Sr(2)CaCu(2)O(8+y), similar to checkerboard patterns in the local density of electronic states reported from scanning tunneling microscope experiments. We have determined both the spin-modulation amplitude and decay length from the vortex core in fields up to H=30 T. 相似文献
89.
A simple electrochemical process has been implemented to fabricated fractal structured leaf-like metallic zinc. The fabricated material was structurally characterized using X-ray diffraction that reveals the hexagonal unit cell structure. Also the growth of the structure is anisotropic. Field emission scanning electron microscopic images revealed clearly the leaf-like morphology of the fabricated material is fern like and ∼500 μm in length, ∼50-60 μm wide and the platelets thickness is ∼5 μm. The growth of this structure is diffusion controlled and locally accomplished with the oriented attachment. Raman shift measurement revealed the existence of surface optical phonon modes which is very significant for surface defects. 相似文献
90.
Basak R Mukhopadhyay N Bandyopadhyay R 《The European physical journal. E, Soft matter》2011,34(9):103
Photon correlation spectroscopy and rheological measurements are performed to investigate the microscopic dynamics and mechanical
responses of aqueous solutions of triblock copolymers and aqueous mixtures of triblock copolymers and anionic surfactants.
Increasing the concentration of triblock copolymers results in a sharp increase in the magnitude of the complex moduli characterising
the samples. This is understood in terms of the changes in the aggregation and packing behaviours of the copolymers and the
constraints imposed upon their dynamics due to increased close packing. The addition of suitable quantities of an anionic
surfactant to a strongly elastic copolymer solution results in a decrease in the complex moduli of the samples by several
decades. It is argued that the shape anisotropy and size polydispersity of the micelles comprising mixtures cause dramatic
changes in the packing behaviour, resulting in sample unjamming and the observed decrease in complex moduli. Finally, a phase
diagram is constructed in the temperature-surfactant concentration plane to summarise the jamming-unjamming behaviour of aggregates
constituting triblock copolymer-anionic surfactant mixtures. 相似文献