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121.
122.
This paper concerns with the investigation of laminar flow separation and its consequences in a tube over a smooth expansion under the axi-symmetric approximations. A co-ordinate stretching has been made to map the expanded tube into a straight tube. The two-dimensional unsteady Navier-Stokes equations are solved approximately by using primitive variables in staggered grid. A thorough quantitative analysis is performed through numerical simulations of the desired quantities such as wall shear stress, axial velocity, pressure distribution etc. These quantities are presented graphically and their consequences in the flow field are analysed in details. The dependence of the flow field on the physical parameter like expansion height d and on the Reynolds number has been investigated in details. It is interesting to note that the peak value of wall shear stress decreases with increasing height of expansion and also with the increasing Reynolds number. 相似文献
123.
124.
Operational characteristics of a dual gain single cavity Nd:YVO4 laser have been investigated. With semiconductor diode laser pump power of 2 W, 800 mW output was obtained with a slope efficiency
of 49%. Further, by changing the relative orientation of the two crystals the polarization characteristics of the output could
be varied. In particular by keeping the two Nd:YVO4 crystals with their c-axes orthogonal to each other and adjusting the gain of the crystals so that both operate at approximately the same power
level, completely unpolarized beams could be obtained. 相似文献
125.
Waves that occur at the surface of a falling film of thin power-law fluid on a vertical plane are investigated. Using the method of integral relations an evolution equation is derived for two types of waves equation which are possible under long wave approximation. This equation reveals the presence of both kinematic and dynamic wave processes which may either act together or singularly dominate the wave field depending on the order of different parameters. It is shown that, at a small flow rate, kinematic waves dominate the flow field and the energy is acquired from the mean flow during the interaction of the waves, while, for high flow rate, inertial waves dominate and the energy comes from the kinematic waves. It is also found that this exchange of energy between kinematic and inertial waves strongly depends on the power-law index n. Linear stability analysis predicts the contribution of different terms in the wave mechanism. Further, it is found that the surface tension plays a double role: for a kinematic wave process, it exerts dissipative effects so that a finite amplitude case may be established, but for a dynamic wave process it yields dispersion. Further, it is shown that the non-Newtonian character n plays a vital role in controlling the role of the term that contains surface tension in the above processes. 相似文献
126.
Pandey R Ghosh S Mukhopadhyay S Ramasesha S Das PK 《The Journal of chemical physics》2011,134(4):044533
We report large quadratic nonlinearity in a series of 1:1 molecular complexes between methyl substituted benzene donors and quinone acceptors in solution. The first hyperpolarizability, β(HRS), which is very small for the individual components, becomes large by intermolecular charge transfer (CT) interaction between the donor and the acceptor in the complex. In addition, we have investigated the geometry of these CT complexes in solution using polarization resolved hyper-Rayleigh scattering (HRS). Using linearly (electric field vector along X direction) and circularly polarized incident light, respectively, we have measured two macroscopic depolarization ratios D=I(2ω,X,X)/I(2ω,Z,X) and D(')=I(2ω,X,C)/I(2ω,Z,C) in the laboratory fixed XYZ frame by detecting the second harmonic scattered light in a polarization resolved fashion. The experimentally obtained first hyperpolarizability, β(HRS), and the value of macroscopic depolarization ratios, D and D('), are then matched with the theoretically deduced values from single and double configuration interaction calculations performed using the Zerner's intermediate neglect of differential overlap self-consistent reaction field technique. In solution, since several geometries are possible, we have carried out calculations by rotating the acceptor moiety around three different axes keeping the donor molecule fixed at an optimized geometry. These rotations give us the theoretical β(HRS), D and D(') values as a function of the geometry of the complex. The calculated β(HRS), D, and D(') values that closely match with the experimental values, give the dominant equilibrium geometry in solution. All the CT complexes between methyl benzenes and chloranil or 1,2-dichloro-4,5-dicyano-p-benzoquinone investigated here are found to have a slipped parallel stacking of the donors and the acceptors. Furthermore, the geometries are staggered and in some pairs, a twist angle as high as 30° is observed. Thus, we have demonstrated in this paper that the polarization resolved HRS technique along with theoretical calculations can unravel the geometry of CT complexes in solution. 相似文献
127.
Chakraborty M Singh NJ Mandal PC Das S Mukhopadhyay S 《The journal of physical chemistry. A》2011,115(19):4882-4893
Described in this work is the kinetics of oxidation of ascorbic acid and hydroquinone by a tetranuclear Mn(IV) oxidant, [Mn(4)(μ-O)(6)(bipy)(6)](4+) (1(4+), bipy =2,2(/)-bipyridine), in aqueous solution over a wide pH range 1.5-6.0. In particular, below pH 3.0, protonation on the oxo-bridge of 1(4+) results in the formation of [Mn(4)(μ-O)(5)(μ-OH)(bipy)(6)](5+) (1H(5+)) as an additional oxidant over 1(4+). Both ascorbic acid and ascorbate whereas only hydroquinone and none of its protolytic species were found to be reactive reducing agents in these reactions. Analysis of the rate data clearly established that the oxo-bridge protonated oxidant 1H(5+) is kinetically far more superior to 1(4+) in oxidizing ascorbic acid and hydroquinone. Rates of these reactions are substantially lowered in D(2)O-enriched media in comparison to that in H(2)O media. An initial one electron one proton transfer electroprotic rate step could be mechanistically conceived. DFT studies established that among the two sets of terminal and central Mn(IV) atoms in the tetranuclear oxidant, one of the two terminal Mn(IV) is reduced to Mn(III) at the rate step that we can intuitively predict considering the probable positive charge distribution on the Mn(IV) atoms. 相似文献
128.
Sukul PK Asthana D Mukhopadhyay P Summa D Muccioli L Zannoni C Beljonne D Rowan AE Malik S 《Chemical communications (Cambridge, England)》2011,47(43):11858-11860
We report unique and spontaneous formation of hydrogels of perylene derivatives with melamine. The luminescent gel network is formed by H-type aggregation of the perylene core, supramolecularly cross-linked by melamine units. As a result of controlled aggregation in the extended nanofibers, strong exciton fluorescence emission is observed. 相似文献
129.
Nidhi Joshi Anindita Mukhopadhyay Sujit Basak Goutam De Krishnananda Chattopadhyay 《Particle & Particle Systems Characterization》2013,30(8):683-694
The presence of magnetic nanoparticles (NPs) in physiological systems induces toxicity through its effects on mitochondrial function and reactive oxygen species (ROS) imbalance. Magnetic NP induced cytotoxicity has been elaborately evaluated for impending threats, however, a detailed investigation is lacking. It is shown that the interaction of Fe3O4 NPs with cytochrome c can lead to different events based on the NPs to protein ratio, the solution conditions, and the type of surface protection. At low NPs concentration, rapid binding and subsequent electron transfer are the preferred events while at higher concentration slow oxidative modification of the protein is initiated. The slow event of protein modification yields conformational disorientation, loss of stability, and formation of amyloid‐like structures with cytochrome c. The possibility that the NP induced oxidative stress and age can work in concert to compromise different aspects of cellular quality control processes is discussed. Suitable surface modifications of the NPs inhibit their direct binding to the protein molecules and minimize NP induced toxicity. 相似文献
130.
B. K. Mukhopadhyay K. K. Ahlquist V. Gruenman A. Lutz I. I. Kovalevski B. Schulze E. Rieger A. Noll W. Nagel J. Grant A. Abrams P. W. Codwise W. Staedel und J. D. Piper 《Fresenius' Journal of Analytical Chemistry》1936,105(5-6):212-222
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