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31.
Adsorption of Triton X-100 (TX-100) on silica gel has been studied as a function of temperature (308–328 K) and composition
for mixtures of water with ethanol or t-butanol. The adsorption capacity of silica gel for TX-100 decreases with increase
in alcohol content. Adsorption isotherms of TX-100 on silica gel are four-region and were analyzed using the ARIAN (adsorption
isotherm regional analysis) model. Data in regions 2, 3 and 4 were fitted to the Temkin, bilayer and reverse desorption isotherms,
respectively. The results show that adsorption of TX-100 on silica gel in water and alcohol-water binary mixtures occurs mainly
through formation of monolayer surface aggregates or low bilayer coverage.
相似文献
32.
Babak Bagheri L. Ridgway Scott Shangyou Zhang 《Finite Elements in Analysis and Design》1994,16(3-4):175-189
We present theoretical analyses of and detailed timings for two programs which use high-order finite element methods to solve the Navier- Strokes equations in two and three dimensions. The analyses show that algorithms popular in low-order finite element implementations are not always appropriate for high-order methods. The timings show that with the proper algorithms high-order finite element methods are viable for solving the Navier-Stokes equations. We show that it is more efficient, both in time and storage, not to precompute element matrices as the degree of approximating functions increases. We also study the cost of assembling the stiffness matrix versus directly evaluating bilinear forms in two and three dimensions. We show that it is more efficient not to assemble the full stiffness matrix for high-order methods in some cases. We consider the computational issues with regard to both Euclidean and isoparametric elements. We show that isoparametric elements may be used with higher-order elements without increasing the order of computational complexity. 相似文献
33.
Highly Stereoselective Intermolecular Haloetherification and Haloesterification of Allyl Amides 下载免费PDF全文
Bardia Soltanzadeh Dr. Arvind Jaganathan Dr. Richard J. Staples Prof. Dr. Babak Borhan 《Angewandte Chemie (International ed. in English)》2015,54(33):9517-9522
An organocatalytic and highly regio‐, diastereo‐, and enantioselective intermolecular haloetherification and haloesterification reaction of allyl amides is reported. A variety of alkene substituents and substitution patterns are compatible with this chemistry. Notably, electronically unbiased alkene substrates exhibit exquisite regio‐ and diastereoselectivity for the title transformation. We also demonstrate that the same catalytic system can be used in both chlorination and bromination reactions of allyl amides with a variety of nucleophiles with little or no modification. 相似文献
34.
Semenenko A. N. Babak N. L. Gella I. M. Musatov V. I. Shishkina S. V. Sofronov D. S. Lipson V. V. 《Russian Journal of Organic Chemistry》2017,53(2):282-289
Russian Journal of Organic Chemistry - Crotone condensation of allobetulone with fluorine-containing benzaldehydes afforded new α,β-unsaturated ketones of lupane series. Their... 相似文献
35.
Kulshrestha A Schomaker JM Holmes D Staples RJ Jackson JE Borhan B 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(44):12326-12339
Good to excellent stereoselectivity has been found in the addition reactions of Grignard and organozinc reagents to N-protected aziridine-2-carboxaldehydes. Specifically, high syn selectivity was obtained with benzyl-protected cis, tert-butyloxycarbonyl-protected trans, and tosyl-protected 2,3-disubstituted aziridine-2-carboxaldehydes. Furthermore, rate and selectivity effects of ring substituents, temperature, solvent, and Lewis acid and base modifiers were studied. The diastereomeric preference of addition is dominated by the substrate aziridines' substitution pattern and especially the electronic character and conformational preferences of the nitrogen protecting groups. To help rationalize the observed stereochemical outcomes, conformational and electronic structural analyses of a series of model systems representing the various substitution patterns have been explored by density functional calculations at the B3LYP/6-31G* level of theory with the SM8 solvation model to account for solvent effects. 相似文献
36.
A novel SBA-15-functionalized TEMPO confined ionic liquid [BMIm]Br was found to be a highly efficient and recyclable catalyst system for the transition-metal-free aerobic oxidation of a wide range of structurally diverse alcohols. Thanks to the strong physical confinement of the ionic liquid inside the mesochannels of SBA-15-supported TEMPO, the resulting solid catalyst showed improved selectivity in the aerobic oxidation of allylic alcohols. The catalyst can be recovered and re-used for at least 11 reaction runs without significant loss of either activity or confined IL. 相似文献
37.
Hydrogen peroxide was employed as the terminal oxidant in the osmium tetroxide mediated oxidative cleavage of olefins, producing the corresponding aldehyde and ketone products. Aryl olefins are cleaved in good to excellent yield regardless of arene electronics. Alkyl olefins cleave in moderate to good yield for di- and tri-substituted alkenes. 相似文献
38.
Let M1,…,Mn be right modules over a ring R. Suppose that the endomorphism ring of each module Mi has at most two maximal right ideals. Is it true that every direct summand of M1⊕?⊕Mn is a direct sum of modules whose endomorphism rings also have at most two maximal right ideals? We show that the answer is negative in general, but affirmative under further hypotheses. The endomorphism ring of uniserial modules, that is, the modules whose lattice of submodules is linearly ordered under inclusion, always has at most two maximal right ideals, and Pavel P?íhoda showed in 2004 that the answer to our question is affirmative for direct sums of finitely many uniserial modules. 相似文献
39.
We investigate the interaction between multiple arrays of (reverse) von Kármán streets as a model for the mid-wake regions produced by schooling fish. There exist configurations where an infinite array of vortex streets is in relative equilibrium, that is, the streets move together with the same translational velocity. We examine the topology of the streamline patterns in a frame moving with the same translational velocity as the streets. Fluid is advected along different paths depending on the distance separating two adjacent streets. When the distance between the streets is large enough, each street behaves as a single von Kármán street and fluid moves globally between two adjacent streets. When the streets get closer to each other, the number of streets that enter into partnership in transporting fluid among themselves increases. This observation motivates a bifurcation analysis which links the distance between streets to the maximum number of streets transporting fluid among themselves. We describe a scaling law relating the number of streets that enter into partnership as a function of the three main parameters associated with the system, two associated with each individual street (determining the aspect ratio of the street), and a third associated with the distance between neighboring streets. In the final section we speculate on the timescale associated with the lifetime of the coherence of this mid-wake scaling regime. 相似文献
40.
Mohammadhassan Vasheghani Ehsan Marzbanrad Cyrus Zamani Mohamed Aminy Babak Raissi Toraj Ebadzadeh Hadi Barzegar-Bafrooei 《Heat and Mass Transfer》2011,47(11):1401-1405
Thermal conductivity of α-Al2O3 was measured using hot wire method. α-Al2O3 (20 nm in size) was synthesized by microwave method for which, the results were compared with commercially available γ-Al2O3. Thermal conductivity of nanofluids was investigated considering, it is dependency on Al2O3 phase. It was observed that by adding 3 wt% of nano γ-Al2O3 and α-Al2O3 to the engine oil, thermal conductivity increases by 37 and 31%, respectively. The corresponding viscosity increase for the
same amount of nano γ-Al2O3 and α-Al2O3 were 36 and 38%, respectively. It was concluded that the differences in thermal conductivity originate from higher specific
surface area of γ-Al2O3 compared to the α-Al2O3 which is the result of porosity difference, obtained during the synthesis process. 相似文献