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排序方式: 共有371条查询结果,搜索用时 187 毫秒
1.
Statistical Inference for Stochastic Processes - We propose a randomized approach to the consistent statistical analysis of random processes and fields on $${\mathbb {R}}^m$$ and $${\mathbb {Z}}^m,... 相似文献
2.
Supramolecular Recognition Influences Magnetism in [X@HVIV8VV14O54]6− Self‐Assemblies with Symmetry‐Breaking Guest Anions 下载免费PDF全文
Dr. Kirill Yu. Monakhov Oliver Linnenberg Dr. Piotr Kozłowski Dr. Jan van Leusen Dr. Claire Besson Tim Secker Dr. Arkady Ellern Dr. Xavier López Prof. Dr. Josep M. Poblet Prof. Dr. Paul Kögerler 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(6):2387-2397
Mixed‐valence polyoxovanadates(IV/V) have emerged as one of the most intricate class of supramolecular all‐inorganic host species, able to encapsulate a wide variety of smaller guest templates during their self‐assembly formation process. As showcased herein, the incorporation of guests, though governed solely by ultra‐weak electrostatic and van der Waals interactions, can cause drastic effects on the electronic and magnetic characteristics of the shell complex of the polyoxovanadate. We address the question of methodology for the magnetochemical analysis of virtually isostructural {VIV/V22O54}‐type polyoxoanions of D2d symmetry enclosing diamagnetic VO2F2? (C2v), SCN? (C∞v), or ClO4? (Td) template anions. These induce different polarization effects related to differences in their geometric structures, symmetry, ion radii, and valence shells, eventually resulting in a supramolecular modulation of magnetic exchange between the V(3d) electrons that are partly delocalized over the {V22O54} shells. We also include the synthesis and characterization of the novel [VVO2F2@HVIV8VV14O54]6? system that comprises the rarely encountered discrete difluorovanadate anion as a quasi‐isolated guest species. 相似文献
3.
Stanislav Kozin Vladimir Skrebitsky Rodion Kondratenko Alexander Kravtsov Elena Butina Arkady Moiseev Vadim Malyshko Mikhail Baryshev Anna Elkina Stepan Dzhimak 《Molecules (Basel, Switzerland)》2021,26(7)
The deuterium content modification in an organism has a neuroprotective effect during the hypoxia model, affecting anxiety, memory and stress resistance. The aim of this work was to elucidate the possible mechanisms of the medium D/H composition modification on nerve cells. We studied the effect of an incubation medium with a 50 ppm deuterium content compared to a medium with 150 ppm on: (1) the activity of Wistar rats’ hippocampus CA1 field neurons, (2) the level of cultured cerebellar neuron death during glucose deprivation and temperature stress, (3) mitochondrial membrane potential (MMP) and the generation of reactive oxygen species in cultures of cerebellar neurons. The results of the analysis showed that the incubation of hippocampal sections in a medium with a 50 ppm deuterium reduced the amplitude of the pop-spike. The restoration of neuron activity was observed when sections were returned to the incubation medium with a 150 ppm deuterium content. An environment with a 50 ppm deuterium did not significantly affect the level of reactive oxygen species in neuron cultures, while MMP decreased by 16–20%. In experiments with glucose deprivation and temperature stress, the medium with 50 ppm increased the death of neurons. Thus, a short exposure of nerve cells in the medium with 50 ppm deuterium acts as an additional stressful factor, which is possibly associated with the violation of the cell energy balance. The decrease in the mitochondrial membrane potential, which is known to be associated with ATP synthesis, indicates that this effect may be associated with the cell energy imbalance. The decrease in the activity of the CA1 field hippocampal neurons may reflect reversible adaptive changes in the operation of fast-reacting ion channels. 相似文献
4.
Maxim V. Musalov Vladimir A. Potapov Vladimir A. Yakimov Maria V. Musalova Arkady A. Maylyan Sergey V. Zinchenko Svetlana V. Amosova 《Molecules (Basel, Switzerland)》2021,26(12)
The regioselective synthesis of novel functionalized condensed organochalcogen compounds by chalcogenocyclofunctionalization reactions based on chalcogen halides and the natural products thymol and carvacrol has been developed. The reactions of selenium dibromide with allyl thymol and allyl carvacrol proceeded in methylene chloride at room temperature in the presence of NaHCO3 affording bis[(7-isopropyl-4-methyl-2,3-dihydro-1-benzofuran-2-yl)methyl] and bis[(4-isopropyl-7-methyl-2,3-dihydro-1-benzofuran-2-yl)methyl] selenides in 90–92% yield. Similar sulfides were obtained in 70–72% yields by the reaction of sulfur dichloride in chloroform under reflux. Trihalotellanes containing the same organic moieties were synthesized from allyl thymol, allyl carvacrol and tellurium tetrachloride or tetrabromide in quantitative yields. Corresponding functionalized ditellurides were prepared in 91–92% yields by the reduction of the trichlorotellanes with sodium metabisulfite in two-phase solvent system. The comparison of reactivity of sulfur, selenium and tellurium halides in chalcogenocyclofunctionalization and distinguishing features of each reaction were discussed. 相似文献
5.
Evaporation of groundwater in a region with a shallow water table and small natural replenishment causes accumulation of salts near the ground surface. Water in the upper soil layer becomes denser than in the depth. This is a potentially unstable situation which may result in convective currents. When free convection takes place, estimates of the salinity profile, salt precipitation rate, etc., obtained within the framework of a 1-D (vertical) model fail.Very simplified model of the process is proposed, in which the unsaturated zone is represented by a horizontal soil layer at a constant water saturation, and temperature changes are neglected. The purpose of the model is to obtain a rough estimate of the role of natural convection in the salinization process.A linear stability analysis of a uniform vertical flow is given, and the stability limit is determined numerically as a function of evaporation rate, salt concentration in groundwater, and porous medium dispersivity. The loss of stability corresponds to quite realistic Rayleigh numbers. The stability limit depends in nonmonotonic way on the evaporation rate.The developed convective regime was simulated numerically for a 2-D vertical domain, using finite volume element discretization and FAS multigrid solver. The dependence of the average salt concentration in the upper layer on the Rayleigh number was obtained.List of Main Symbols
horizontal wavenumber
-
L
,
T
dispersivities (longitudinal and transversal)
-
D
*
diffusion coefficient (in a porous medium)
-
g
acceleration of gravity
-
H
thickness of the vadoze zone
-
k
permeability
-
p
pressure
- Pe
Péclet number
-
q
mass flux
- Ra
Rayleigh number
Greek
L
,
T
dimensionless dispersivities
-
coefficient of concentration expansion
-
coefficient of viscosity variation
-
volumetric fraction of the liquid phase
-
viscosity
-
density
-
stream function
-
mass fraction of salt in water
Vectors and tensors
D
dispersion coefficient
-
e
unit vector
-
I
unit tensor
-
J
nonadvective salt flux
-
V
liquid phase velocity
-
x
radius-vector 相似文献
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8.
Iurie L. Malaestean Sebastian Schmitz Arkady Ellern Paul Kgerler 《Acta Crystallographica. Section C, Structural Chemistry》2013,69(10):1144-1146
The structure of the title compound, {[Mg(C4H7O2)2(H2O)3]·H2O}n, features one‐dimensional ...(μ2‐ib)Mg(μ2‐ib)Mg... zigzag chains (ib is isobutyrate) parallel to the c axis. The octahedral Mg environment is completed by three fac‐oriented terminal water ligands, as well as one further monodentate end‐on coordinated ib ligand. In the crystal structure, the hydrophobic ib groups are all oriented within one half of the coordination perimeter of each chain, whereas the water ligands, together with hydrogen‐bonded noncoordinated solvent water molecules, define the other half. Along the a axis, neighbouring strands are oriented so that both the hydrophilic and hydrophobic sides are adjacent to each other. This results in an extensive hydrogen‐bonding network within the hydrophilic areas, also involving an additional solvent water molecule per formula unit. There are van der Waals contacts between the aliphatic isopropyl groups of the hydrophobic areas. 相似文献
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