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831.
Qihui Li Don Hadwin Jiankui Li Xiujuan Ma Junhao Shen 《Functional Analysis and Its Applications》2016,50(1):39-47
In the paper, we consider the question as to whether a unital full amalgamated free product of quasidiagonal C*-algebras is itself quasidiagonal. We give a sufficient condition for a unital full amalgamated free product of quasidiagonal C*-algebras with amalgamation over a finite-dimensional C*-algebra to be quasidiagonal. By applying this result, we conclude that the unital full free product of two AF algebras with amalgamation over a finite-dimensional C*-algebra is AF if there exists a faithful tracial state on each of the two AF algebras such that the restrictions of these states to the common subalgebra coincide. 相似文献
832.
Geramita K McBee J Tao Y Segalman RA Tilley TD 《Chemical communications (Cambridge, England)》2008,(41):5107-5109
The synthesis, optical, electrochemical and physical characterization of 2,7-bis(pentafluorophenylethynyl)hexafluoroheterofluorenes is described along with a preliminary evaluation of their performance in photovoltaic applications. 相似文献
833.
A Sieverts' apparatus coupled with a residual gas analysis is used to measure the concentration variations of hydrogen isotopes in the gas and solid phases during exchange and isothermal decomposition of mixed hydrides. beta-phase palladium hydrides with known ratios of H:D, Pd(H x D 1- x ) y (0 < x < 1, y > 0.6), are prepared by H 2 with PdD y or D 2 with PdH y exchange, and their desorption isotherms are reported here at 323 K. A higher equilibrium pressure in isothermal desorption of mixed hydrides is associated with a higher ratio of D/H in the initial mixed hydrides in beta-phase. The composition of the gas desorbed from a mixed hydride varies; i.e., the ratio of D/H in gas decreases with the sum of (H + D) in Pd. The values of the separation factor alpha during desorption at 323 K and during H-D exchange at 248 K are discussed and compared with those in the literature. Desorption isotherms of mixed isotope hydrides are between those of the single isotope hydrides of H-Pd and D-Pd, however, plateaus slope more than those of pure isotope hydrides. The origin of the plateau sloping in the mixed hydrides can be attributed to the compositional variations during desorption, i.e., the equilibrium pressure is greater when D/H ratio in solid is greater. A simple model is proposed in this study that agrees well with experimental results. 相似文献
834.
Acryloyl chlorides, aldehydes, and PhSLi undergo a direct aldol cascade sequence in the presence of MgBr2 x OEt2 via in situ derived thioester enolates, which is followed by oxidative elimination to give alpha-alkenyl-beta'-hydroxy thioesters. Overall, the procedure is rapid, efficient, and generally applicable, even to beta-substituted acryloyl chlorides, thus providing an alternative to the Morita-Baylis-Hillman reaction with substantially greater synthetic scope and utility. 相似文献
835.
Michael Ben‐or Don Coppersmith Mike Luby Ronitt Rubinfeld 《Random Structures and Algorithms》2008,32(1):49-70
In this paper, we study two questions related to the problem of testing whether a function is close to a homomorphism. For two finite groups G,H (not necessarily Abelian), an arbitrary map f : G,H, and a parameter 0 < ε < 1, say that f is ε‐close to a homomorphism if there is some homomorphism g such that g and f differ on at most ε | G | elements of G, and say that f is ε‐far otherwise. For a given f and ε, a homomorphism tester should distinguish whether f is a homomorphism, or if f is ε‐far from a homomorphism. When G is Abelian, it was known that the test which picks O(1/ε) random pairs x,y and tests that f(x) + f(y) = f(x + y) gives a homomorphism tester. Our first result shows that such a test works for all groups G. Next, we consider functions that are close to their self‐convolutions. Let A = {ag | g ε G} be a distribution on G. The self‐convolution of A, A′ = {a | g ε G}, is defined by It is known that A= A′ exactly when A is the uniform distribution over a subgroup of G. We show that there is a sense in which this characterization is robust—that is, if A is close in statistical distance to A′, then A must be close to uniform over some subgroup of G. Finally, we show a relationship between the question of testing whether a function is close to a homomorphism via the above test and the question of characterizing functions that are close to their self‐convolutions. © 2007 Wiley Periodicals, Inc. Random Struct. Alg., 2008 相似文献
836.
The high-resolution (0.001 cm(-1)) spectrum of thiirane has been recorded at the far-infrared beamline at the Australian synchrotron between 760-400 cm(-1) and 170-10 cm(-1). Ro-vibrational transitions of the highly Coriolis coupled ν(5) (628.1 cm(-1)) and ν(15) (669.7 cm(-1)) fundamentals, as well as pure rotational far-IR transitions have been assigned, and rotational, centrifugal distortion, and Coriolis interaction parameters determined. ν(15) gains the vast majority of its intensity from an interesting Coriolis intensity stealing mechanism, which is also outlined. 相似文献
837.
Sakurai S Nishino H Futaba DN Yasuda S Yamada T Maigne A Matsuo Y Nakamura E Yumura M Hata K 《Journal of the American Chemical Society》2012,134(4):2148-2153
Here we show that essentially any Fe compounds spanning Fe salts, nanoparticles, and buckyferrocene could serve as catalysts for single-walled carbon nanotube (SWNT) forest growth when supported on AlO(x) and annealed in hydrogen. This observation was explained by subsurface diffusion of Fe atoms into the AlO(x) support induced by hydrogen annealing where most of the deposited Fe left the surface and the remaining Fe atoms reconfigured into small nanoparticles suitable for SWNT growth. Interestingly, the average diameters of the SWNTs grown from all iron compounds studied were nearly identical (2.8-3.1 nm). We interpret that the offsetting effects of Ostwald ripening and subsurface diffusion resulted in the ability to grow SWNT forests with similar average diameters regardless of the initial Fe catalyst. 相似文献
838.
Wright RJ Zhang W Yang X Fasulo M Tilley TD 《Dalton transactions (Cambridge, England : 2003)》2012,41(1):73-82
Proposed electrocatalytic proton reduction intermediates of hydrogenase mimics were synthesized, observed, and studied computationally. A new mechanism for H(2) generation appears to involve Fe(2)(CO)(6)(1,2-S(2)C(6)H(4)) (3), the dianions {[1,2-S(2)C(6)H(4)][Fe(CO)(3)(μ-CO)Fe(CO)(2)](2-) (3(2-)), the bridging hydride {[1,2-S(2)C(6)H(4)][Fe(CO)(3)(μ-CO)(μ-H)Fe(CO)(2)]}(-), 3H(-)(bridging), and the terminal hydride 3H(-)(term-stag), {[1,2-S(2)C(6)H(4)][HFe(CO)(3)Fe(CO)(3)]}(-), as intermediates. The dimeric sodium derivative of 3(2-), {[Na(2)(THF)(OEt(2))(3)][3(2-)]}(2) (4) was isolated from reaction of Fe(2)(CO)(6)(1,2-S(2)C(6)H(4)) (3) with excess sodium and was characterized by X-ray crystallography. It possesses a bridging CO and an unsymmetrically bridging dithiolate ligand. Complex 4 reacts with 4 equiv. of triflic or benzoic acid (2 equiv. per Fe center) to generate H(2) and 3 in 75% and 60% yields, respectively. Reaction of 4 with 2 equiv. of benzoic acid generated two hydrides in a 1.7 : 1 ratio (by (1)H NMR spectroscopy). Chemical shift calculations on geometry optimized structures of possible hydride isomers strongly suggest that the main product, 3H(-)(bridging), possesses a bridging hydride ligand, while the minor product is a terminal hydride, 3H(-)(term-stag). Computational studies support a catalytic proton reduction mechanism involving a two-electron reduction of 3 that severs an Fe-S bond to generate a dangling thiolate and an electron rich Fe center. The latter iron center is the initial site of protonation, and this event is followed by protonation at the dangling thiolate to give the thiol thiolate [Fe(2)H(CO)(6)(1,2-SHSC(6)H(4))]. This species then undergoes an intramolecular acid-base reaction to form a dihydrogen complex that loses H(2) and regenerates 3. 相似文献
839.
McDermott TC Akter T MacElroy JM Mooney DA McCann MT Dowling DP 《Langmuir : the ACS journal of surfaces and colloids》2012,28(1):506-516
In this work the origin of permselectivity in dense silica films which possess a pore structure with pore sizes commensurate with the molecular size of the diffusing gas species is investigated. Much of the recently reported work in this field has involved the development of composite membrane films, and while it is generally assumed that the transport process of the gas species within the selective layer of these films is activated in nature, there are anomalies with this simplified picture. In this paper a new model is developed which, for the first time, explains the permselective behavior of the thin selective coatings ubiquitous to membrane separation processes. The model involves the existence of two primary transport domains within the solid film, one of which rapidly conducts the permeating gas (under non-Fickian conditions), while the second domain involves a slow diffusion mode characterized by normal Fickian transport. To validate the model, molecular dynamics simulations are conducted for diffusion of a number of simple gases (He, N(2), and CO(2)) within silica glasses over a range of solid densities. The silica media employed in these studies are based on a novel approach developed in this work for the construction of three-dimensionally periodic atomistic structures of silica of arbitrary density in which network bond connectivity is ensured. The results obtained from this work are in qualitative agreement with experimental observations and confirm the existence of dual mode transport which is central to the interpretation of the permselectivity in composite membranes systems. 相似文献
840.
How can a formulator have confidence that a preservative system will perform as expected under adverse conditions? Extreme conditions that can lead to the development of "off odors" in the product can be a serious challenge for companies providing home care products in the global market. Formulation and stability testing occur under controlled parameters that simulate limited environmental conditions and microbial challenges are typically performed with a standard inoculum level. While this is an acceptable and dependable process, it does not necessarily assess how well a preservative system can perform under extreme environmental conditions or against unusually high levels of bacterial challenges. This is especially true when formulations are diluted and stored by the end-user. By modifying microbial challenge testing of a liquid dishwashing product to include unexpected dilution schemes, increased microbial assaults, and elevated temperatures, a pattern of preservative efficacy was established. The resulting approach proved to be a useful tool when developing use directions, recommended dilution levels, the overall surfactant system, preservative type, and storage restrictions. 相似文献