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121.
Magdalena Śliwka-Kaszyńska Grzegorz Gorczyca Marek Ślebioda 《Journal of chromatography. A》2010,1217(3):329-336
Twelve calix[4]arene stationary phases in 1,3-alternate conformation, synthesized in the authors’ laboratory, were characterized in terms of their surface coverage, hydrophobic selectivity, aromatic selectivity, shape selectivity, hydrogen bonding capacity and ion-exchange capacity. The set of tests commonly used for evaluation of commercially available stationary phases was applied to assess fundamental chromatographic properties of the calixarene phases. The new calixarene phases were compared to each other, to Caltrex and LiChrosorb C-18 columns. Principal component analysis has been used to provide comparison between 1,3-alternate calix[4]arene phases and commercially available phenyl, fluorophenyl and fluoroalkyl columns. 相似文献
122.
We study factorization and dilation properties of Markov maps between von Neumann algebras equipped with normal faithful states,
i.e., completely positive unital maps which preserve the given states and also intertwine their automorphism groups. The starting
point for our investigation has been the question of existence of non-factorizable Markov maps, as formulated by C. Anantharaman-Delaroche.
We provide simple examples of non-factorizable Markov maps on
Mn(\mathbbC){M_n(\mathbb{C})} for all n ≥ 3, as well as an example of a one-parameter semigroup (T(t))
t≥0 of Markov maps on
M4(\mathbbC){M_4(\mathbb{C})} such that T(t) fails to be factorizable for all small values of t > 0. As applications, we solve in the negative an open problem in quantum information theory concerning an asymptotic version
of the quantum Birkhoff conjecture, as well as we sharpen the existing lower bound estimate for the best constant in the noncommutative
little Grothendieck inequality. 相似文献
123.
Radomir Jasiński Magdalena Kwiatkowska Andrzej Barański 《Journal of Physical Organic Chemistry》2011,24(9):843-853
In spite of diversified electrophilicity of E‐2‐arylnitroethenes, their [4 + 2] cycloaddition reactions with cyclopentadiene leads to the corresponding 6‐endo‐aryl‐5‐exo‐nitronorbornenes and 6‐exo‐aryl‐5‐endo‐nitronorbornenes as the only reaction products. Stereoselectivity, substituent and solvent effects, and activation parameters, suggest that these reactions occur via a synchronous concerted mechanism on both competing pathways. The experimental results obtained are consistent with the data from B3LYP/6‐31G(d) calculations. Due to high electrophilicity of E‐2‐arylnitroethenes, the reactions studied should be considered as polar [4 + 2] cycloadditions. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
124.
Magdalena Ulmeanu Iuliana Iordache Mihaela Filipescu Valentin Craciun Simona Cinta Pinzaru Andreas Hörner 《Central European Journal of Physics》2011,9(5):1280-1287
Experimental studies on patterning hexagonal Ge nanostructures have been conducted on Si substrates through deposition of
Ge with colloidal particles as a mask. The deposited Ge thin film possesses, according to the X-ray diffraction measurements,
in plane texture, being epitaxial and aligned with the (111) Si substrate. The size distribution of the patterned Ge nanostructures
is narrow, as indicated by the atomic force microscopy and scanning electron microscopy measurements. We have obtained Ge
nanostructures with lateral dimension of 490 nm (height 12 nm), 200 nm (height 6 nm) and 82 nm (height 6 nm) by using different
sizes of polystyrene spheres. We have performed in depth studies of the Ge nanostructures’ behavior due to thermal and rapid
thermal post-annealing processes. FT micro-Raman spectroscopy shows that there is no Si intermixing during the annealing process.
In order to quantify the changes in the height and lateral dimension, we have performed atomic force microscopy and white
light interferometry analysis. The changes in shape and the decrease in the area of a cross-section of Ge nanostructure will
be discussed in respect to similar results shown in the literature for Ge thin films during the annealing process. 相似文献
125.
Agata Roguska Andrzej KudelskiMarcin Pisarek Magdalena OparaMaria Janik-Czachor 《Applied Surface Science》2011,257(19):8182-8189
Tubular arrays of TiO2 nanotubes (ranging in diameter from 40 to 110 nm) on a Ti substrate were used as a support for Ag, Au or Cu deposits obtained by the sputter deposition technique, where the amount of metal varied from 0.01 to 0.2 mg/cm2. Those composite supports were intended for surface-enhanced Raman scattering (SERS) investigations. Composite samples were studied with the aid of scanning electron microscopy (SEM) and Auger electron spectroscopy (AES) to reveal their characteristic morphological and chemical features. Raman spectra of pyridine (as a probe molecule) were measured at different cathodic potentials ranging from −0.2 down to −1.2 V after the pyridine had been adsorbed on the metal-covered TiO2 nanotube/Ti substrates. In addition, SERS spectra on a bulk standard activated Ag, Au and Cu substrates were also measured. The SERS activity of the composite samples was strongly dependent on the amount of metal deposit, e.g. at and above 0.06 mg Ag/cm2, the intensity of SERS signal was even higher than that for the Ag reference substrate. The high activity of these composites is mainly a result of their specific morphology. The high SERS sensitivity on the surface morphology of the substrate made it possible to monitor very small temporal changes in the Ag metal clusters. This rearrangement was not detectable with microscopic (SEM) or microanalytical (AES) methods. The SERS activity of Au or Cu clusters was distinctly lower than those of Ag. The spectral differences exhibited by the three kinds of composites as compared to the reference metal samples are discussed. 相似文献
126.
Paweł K. Zarzycki Magdalena M. ŚlączkaMagdalena B. Zarzycka Elżbieta WłodarczykMichał J. Baran 《Analytica chimica acta》2012
The main goal of present paper is to demonstrate the separation and detection capability of micro-TLC technique involving simple one step liquid extraction protocols of complex materials without multi-steps sample pre-purification. In the present studies target components (cyanobacteria pigments, lipids and fullerenes) were isolated from heavy loading complex matrices including spirulina dried cells, birds’ feathers and fatty oils as well as soot samples derived from biomass fuel and fossils-fired home heating systems. In each case isocratic separation protocol involving less that 1 mL of one component or binary mixture mobile phases can be completed within time of 5–8 min. Sensitive detection of components of interest was performed via fluorescence or staining techniques using iodine or phosphomolybdic acid. Described methodology can be applied for fast fractionation or screening of whole range of target substances as well as chemo-taxonomic studies and fingerprinting of complex mixtures, which are present in raw biological or environmental samples. 相似文献
127.
Marija Mirković Drina Janković Sanja Vranješ‐Đurić Magdalena Radović Dragana Stanković Dušan Mijin Nadežda Nikolić 《应用有机金属化学》2012,26(7):347-355
Two novel diamine dioxime ligands, 4,7‐diaza‐3,8‐diethyldecane‐2,9‐dione bis oxime (3) and 4,9‐diaza‐3,10‐diethyldodecane‐2,11‐dione bis oxime (5), were synthesized in order to develop new brain perfusion imaging agents, based on 99mTc(V)‐complexes. The synthesis involved condensation of 2‐hydroxyimino‐3‐pentanone with appropriate diamine in protic solvent which afforded the bis imine adducts. Subsequent reduction of imine functional groups yielded a diastereoisomeric mixture of 3 and 5. UV–visible, IR, 1H NMR, 13C NMR and elemental analysis were used to characterize the structures of the synthesized compounds. 99mTc‐complexes of both diamine dioximes were prepared and radiolabeling conditions optimized to give the maximum yield. Physicochemical parameters of the labeled complexes as well as and their biodistribution in rats were investigated. Both compounds (3 and 5) formed 99mTc‐complexes with a net charge of zero, determined by electrophoresis. The resultant lipophilic 99mTc‐complexes of 3 and 5 were readily formed at pH ~9.0 within 10 min at room temperature with yields of 90% and 95%, respectively. The 99mTc‐3 complex was found to be stable within 1 h, while 99mTc‐5 was stable for a few hours. A significant brain uptake of 99mTc‐3 (2.1% injected dose) and 99mTc‐5 (1.8% injected dose) complexes, 2 min after injection, is in accordance with their lipophilicity. The present study suggests that both ligands are promising candidates as new 99mTc‐based brain‐imaging agents. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
128.
129.
Magdalena Niziolek-Kierecka Anna Pilat Witold Korytowski Albert W. Girotti 《Photochemistry and photobiology》2010,86(3):681-686
Using a 5-aminolevulinic acid (ALA)-photodynamic therapy model, we have discovered a new effect of nitric oxide (NO)—the ability to accommodate apoptosis. When sensitized by disseminated ALA-generated protoporphyrin IX, COH-BR1 tumor cells in glucose-containing medium died mainly by necrosis with a low level of apoptosis. Introduced before light at a nontoxic concentration, the NO donor SPNO inhibited necrosis, but supported apoptosis such that the latter became predominant in the remaining cell death. Accompanying this was a large increase in caspase-3/7 activation. SPNO-supported apoptosis was more pronounced when glucose-deprived cells were compared with glucose-replenished, SPNO-treated counterparts. SPNO plus glucose also suppressed plasma membrane-damaging lipid peroxidation and loss of cellular ATP under photostress. The NO effect is attributed to membrane protection with maintenance of sufficient glycolytic ATP to sustain apoptosis. 相似文献
130.
Wertheim’s integral equation theory for associating fluids is reformulated for the study of the connectedness properties of
associating hard spheres with four bonding sites. The association interaction is described as a square-well saturable attraction
between these sites. The connectedness version of the Ornstein-Zernike (OZ) integral equation is supplemented by the PY-like
closure relation and solved analytically within an ideal network approximation in which the network is represented as resulting
from the crossing of ideal polymer chains. The pair connectedness functions and the mean cluster size are calculated and discussed.
The condition for the percolation transition and the analytical form of the percolation threshold are derived. The connection
of the percolation with the gas-liquid phase transition is discussed. 相似文献