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221.
Didier Gastmans Vinícius Santos Juliana Aparecida Galhardi João Felipe Gromboni Ludmila Vianna Batista Konrad Miotlinski 《Isotopes in environmental and health studies》2017,53(5):518-538
Based on Global Network Isotopes in Precipitation (GNIP) isotopic data set, a review of the spatial and temporal variability of δ18O and δ2H in precipitation was conducted throughout central and eastern Brazil, indicating that dynamic interactions between Intertropical and South Atlantic Convergence Zones, Amazon rainforest, and Atlantic Ocean determine the variations on the isotopic composition of precipitation over this area. Despite the seasonality and latitude effects observed, a fair correlation with precipitation amount was found. In addition, Hybrid Single-Particle Lagrangian Integrated Trajectory (HYSPLIT) air mass back trajectories were used to quantify the factors controlling daily variability in stable isotopes in precipitation. Through a linear multiple regression analysis, it was observed that temporal variations were consistent with the meteorological parameters derived from HYSPLIT, particularly precipitation amount along the trajectory and mix depth, but are not dependent on vapour residence time in the atmosphere. These findings also indicate the importance of convective systems to control the isotopic composition of precipitation in tropical and subtropical regions. 相似文献
222.
Mahendra Thunga Bhabani K. Satapathy Manfred Stamm Konrad Knoll 《European Polymer Journal》2009,45(2):537-314
The phase behaviour of symmetric (LN4) and asymmetric (LN3) triblock copolymers based on styrene-b-(styrene-co-butadiene)-b-styrene (S-SB-S) and their blends have been studied using transmission electron microscopy (TEM) and small-angle X-ray scattering (SAXS) and were correlated with rheological properties. A direct control over the final morphology and segregation strength for the block copolymer blends was achieved by blending of LN3 and LN4. The interaction parameter (χ) for LN4 is extracted by fitting the SAXS patterns at temperatures well above the ODT in consistency with Leibler mean-field structure-function for ABA triblock copolymers. A weak temperature dependency of χ has been observed which revealed that the phase behaviour in LN4 is mainly controlled by the entropic term. In the low frequency regime a non-terminal flow behaviour was observed in LN3 revealing the persistence of ordered structure within the experimental temperature range whereas a terminal flow behaviour with composition fluctuation was observed in LN4. G′ vs. G″ plots indicated a solid-like elastic melt behaviour for LN3 whereas presence of ODT over a broad temperature range was observed for LN4. ODT is observed to increase non-linearly with increase in LN3 content in the blends. ODT behaviour of the blends further reveals that the blends shift from weak-segregation to intermediate-segregation strength with the increase in LN3 content. The improvement in the state of ordering along with the change in morphology with the increase of LN3 content is attributed to co-surfactant effect between the PS end-blocks of LN3 and LN4 inside PS-rich phase. 相似文献
223.
Konrad Sommer 《Tetrahedron》2009,65(16):3246-7126
The stereocontrolled, asymmetric synthesis of triply deuterium-labeled 7-hydroxy-pre-paraherquamide (27) was accomplished, employing a diastereoselective intramolecular SN2′ cyclization strategy. The deuterium-labeled substrate was interrogated in a precursor incorporation experiment in the paraherquamide-producing organism Penicillium fellutanum. The isolated sample of paraherquamide A revealed incorporation of one of the two geminal deuterons of the CD2-group at C-12 exclusively. The lack of signals for the second deuteron of the CD2-group at C-12 and for the CH2D-group (C-22/C-23) suggests that this substrate suffered an unexpectedly selective catabolic degradation and metabolic re-incorporation of deuterium thus casting doubt on the proposed biosynthetic intermediacy of 27. Consideration of alternative biosynthetic pathways, including oxidation of the indole C-6 position prior to hydroxylation at C-7 or oxidative spiro-contraction of pre-paraherquamide prior to construction of the dioxepin is discussed. The synthesis of 27 also provides for a concise, asymmetric stereocontrolled synthesis of an advanced intermediate that will be potentially useful in the synthesis of paraherquamides E and F. 相似文献
224.
Konrad J. Swanepoel 《Discrete and Computational Geometry》2009,41(1):1-27
We show that the maximum number of unit distances or of diameters in a set of n points in d-dimensional Euclidean space is attained only by specific types of Lenz constructions, for all d≥4 and n sufficiently large depending on d. As a corollary, we determine the exact maximum number of unit distances for all even d≥6 and the exact maximum number of diameters for all d≥4 and all n sufficiently large depending on d.
This material is based upon work supported by the South African National Research Foundation. 相似文献
225.
Balázs Csikós György Kiss Konrad J. Swanepoel P. Oloff de Wet 《Periodica Mathematica Hungarica》2009,58(2):129-138
A family {A
i
| i ∈ I} of sets in ℝ
d
is antipodal if for any distinct i, j ∈ I and any p ∈ A
i
, q ∈ A
j
, there is a linear functional ϕ:ℝ
d
→ ℝ such that ϕ(p) ≠ ϕ(q) and ϕ(p) ≤ ϕ(r) ≤ ϕ(q) for all r ∈ ∪
i∈I
A
i
. We study the existence of antipodal families of large finite or infinite sets in ℝ3.
The research was supported by the Hungarian-South African Intergovernmental Scientific and Technological Cooperation Programme,
NKTH Grant no. ZA-21/2006 and South African National Research Foundation Grant no. UID 61853, as well as Hungarian National
Foundation for Scientific Research Grants no. NK 67867, no. T47102, and no. K72537. 相似文献
226.
Thin-film flows are involved in many coating processes, where it is desirable to achieve thin and homogeneous fluid layers. In the present investigations, we treat droplets, spreading on rotating solid substrates. Micro-scale effects appear, firstly, at the wetting front, where the film height tends to zero. Secondly, micro-scale effects may appear at other locations, where the free liquid/gas-interface approaches the solid substrate, as e.g. at film rupture. For such situations, molecular effects need to be considered, e.g. in form of the disjoining pressure (DJP), to get physically-correct solutions. Otherwise, the spreading can be modeled within the frame of continuum mechanics, augmented by the (empirical) law of Tanner to capture the contact-line dynamics. We present, on the one hand, an overview of several interesting issues, as (i) spreading with and without considering the DJP, (ii) spreading after central rupture, including hysteresis effects, and (iii) non-isothermal spreading, including temperature-dependent surface tension (Marangoni effect) and temperature-dependent density (Rayleigh-Bénard effect). On the other hand, we present results for the instability of the contact line, for which the contact line gets corrugated (under isothermal conditions). This instability goes along with a transition from (rotationally-symmetric) two-dimensional to three-dimensional behavior. (© 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
227.
Photoelectrodes made of nanocrystalline titanium dioxide modified with various pentacyanoferrates exhibit unique photoelectrochemical properties; photocurrent direction can be switched from anodic to cathodic and vice versa upon changes in photoelectrode potential and incident light wavelength (PhotoElectrochemical Photocurrent Switching, PEPS effect). At certain potentials, anodic photocurrent generated upon UV irradiation has the same intensity as the cathodic photocurrent generated upon visible irradiation. Under these conditions, simultaneous irradiation with UV and visible light results in compensation of anodic and cathodic photocurrents, and zero net photocurrent is observed. This process can be used for construction of unique light-driven chemical logic gates. 相似文献
228.
Tietze LF Stecker F Zinngrebe J Sommer KM 《Chemistry (Weinheim an der Bergstrasse, Germany)》2006,12(34):8770-8776
An enantioselective total synthesis of vitamin E in which a novel palladium-catalyzed domino reaction was employed as the key step is described. This reaction allows the formation of the chiral chroman framework and the concurrent introduction of part of the side chain of vitamin E. The sequence comprises an enantioselective Wacker cyclization and a subsequent Heck reaction. Accordingly, reaction of alkenylphenol 12 with methyl vinyl ketone (13) in the presence of catalytic amounts of Pd(OTFA)(2) (TFA = trifluoroacetate), the enantiopure ligand (S,S)-Bn-BOXAX (8 b; Bn = benzyl, BOXAX = 2,2'-bis(oxazolyl)-1,1'-binaphthyl, and p-benzoquinone (9) as an oxidant gives access to chiral chroman 10 with an enantioselectivity of 97 % ee in 84 % yield. Chroman 10 is then converted into 24 by an aldol condensation reaction with (3R)-3,7-dimethyloctanal (11). Subsequent 1,2-addition of methyllithium, elimination of water, and hydrogenation yields vitamin E. 相似文献
229.
Of the four published osmium fluorine compounds in the oxidation state +7, OsO3F, OsO2F3, OsOF5, and OsF7, only one (OsOF5) is a real Os(VII) compound. OsO(3)F has obviously been OsO4. OsO2F3 in its two modifications is a mixed-valence Os(VI)/Os(VIII) compound, whereas a new compound Os2O3F7 is a mixed-valence OsV/Os(VIII) compound. The molecular structures of OsO3F, OsO2F3, and OsO3F2 are calculated. OsO3F2 seems to exist in two forms, with D3h and Cs symmetry. The original preparation of OsF7 could not be reproduced, only OsF6 has been obtained. 相似文献
230.
Density functional calculations for [M(CH3)F5], [M(CF3)F5], [M(CH3S)F5], and [M(CF3S)F5] (M=Mo, W) show that they are expected to be nonrigid molecules, with energy barriers for the octahedral-trigonal-prismatic interchange as low as 7.2 kJ mol(-1). The ground state for the CH3- and CF3- compounds is trigonal prismatic, for the CH3S- and CF3S- compounds, (distorted) octahedral. All calculated compounds [M(C6F5)nF(6-n)] (M=Mo, W) have a trigonal-prismatic ground state, whereas the situation for [M(C6H5)nF(6-n)] (M=Mo, W) is more complex. 相似文献