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211.
Single-shot spectral interferometry with chirped pulses   总被引:1,自引:0,他引:1  
We present a method for obtaining time-resolved measurements of the amplitude modulation and the phase shift of a chirped probe pulse interacting with a femtosecond-laser-produced plasma. Based on spectral interferometry, the technique allows for single-shot measurements and keeps the temporal resolution associated with the full bandwidth of the probe pulse. We demonstrate the efficiency of this technique by probing femtosecond-laser breakdown of plastic targets.  相似文献   
212.
Summary: The lack of accurate knowledge for measuring monomer droplet size and droplet size distribution has hampered the further progress of miniemulsion polymerization. Monomer droplet size is probably the most important characteristics of a miniemulsion, influencing the miniemulsion stability and the nucleation mechanism. To date, several experimental techniques have been tested to measure miniemulsion droplet size, but none are convenient and accurate. This work presents a novel experimental technique, using a powerful new scanning transmission electron microscopy (STEM) imaging system, which allows transmission observations of wet samples in an environmental scanning electron microscopy (ESEM). This new imaging technique is a useful technique to directly measure droplet size and droplet size distribution.

Miniemulsion droplets in dark field wet STEM imaging conditions.  相似文献   

213.
We take advantage of the interpretation of stochastic capacity expansion problems as stochastic equilibrium models for assessing the risk exposure of new equipment in a competitive electricity economy. We develop our analysis on a standard multistage generation capacity expansion problem. We focus on the formulation with nonanticipativity constraints and show that their dual variables can be interpreted as the net margin accruing to plants in the different states of the world. We then propose a procedure to estimate the distribution of the Lagrange multipliers of the nonanticipativity constraints associated with first stage decisions; this gives us the distribution of the discounted cash flow of profitable plants in that stage.  相似文献   
214.
Abstract

The variation of the elastic constant of an oriented C6H6 monocrystal shows the occ urenre of an irreversible process above 20 GPa. This process leads to the format ion of a polymer- as it was shown by IR study. The bulk modulus of the recovered product is one order of magni t ude above that of solid benzene, this gives ev idence for a reconstruct ion of the bonds in the sample.

La mesure de constantes élastiques réalisée sur un monocristal orienté de benzene montre qu' un processus irréversible se développe au-delá de 20 GPa. La formation d'un Polymére Peut ětre constatée aprés I'exdpérience. Le module de rigidité du produit formé, un ordre de grandeur au-dessus de Celui du benzene solide, montre clairement qu'une reconstruction des liaisons a eu lieu.  相似文献   
215.
216.
The synthesis of arborescent styrenic homopolymers and copolymers was achieved by anionic polymerization and grafting. Styrene and p‐(3‐butenyl)styrene were first copolymerized using sec‐butyllithium in toluene, to generate a linear copolymer with a weight‐average molecular weight Mw = 4000 and Mw/Mn = 1.05. The pendant double bonds of the copolymer were then epoxidized with m‐chloroperbenzoic acid. A comb‐branched (or arborescent generation G0) copolymer was obtained by coupling the epoxidized substrate with living styrene‐p‐(3‐butenyl)styrene copolymer chains with Mw ≈ 5000 in a toluene/tetrahydrofuran mixture. Further cycles of epoxidation and coupling reactions while maintaining Mw ≈ 5000 for the side chains yielded arborescent copolymers of generations G1–G3. A series of arborescent styrene homopolymers was also obtained by grafting Mw ≈ 5000 polystyrene side chains onto the linear and G0–G2 copolymer substrates. Size exclusion chromatography measurements showed that the graft polymers have low polydispersity indices (Mw/Mn = 1.02–1.15) and molecular weights increasing geometrically over successive generations. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012  相似文献   
217.
Communications in Mathematical Physics - We study the controllability of a closed control-affine quantum system driven by two or more external fields. We provide a sufficient condition for...  相似文献   
218.
We consider several settings for C m -subharmonic extension and C m -harmonic approximation problems of Runge type in Euclidean domains.  相似文献   
219.
Amphiphilic copolymers were obtained by grafting arborescent poly(γ‐benzyl l ‐glutamate) (PBG) cores of generations G1–G3 with polyglycidol, poly(ethylene oxide) (PEO), or poly(l ‐glutamic acid) (PGA) chain segments. The PBG substrates were synthesized by two methods: (1) subjecting PBG samples with a dispersity ? = Mw/Mn < 1.1 to partial acidolysis of the benzyl ester groups, to produce randomly distributed carboxylic acid functionalities, and (2) using PBG chains containing a glutamic acid di‐tert‐butyl ester initiator fragment in the last grafting cycle of the PBG core synthesis, and selective acidolysis of the tert‐butyl ester groups to obtain substrates with carboxylic acid termini. Linear polymers with ? < 1.20 and a primary amine terminus were also synthesized to serve as hydrophilic shell materials: Polyglycidol and PEO by anionic polymerization, and PGA by N‐carboxyanhydride ring‐opening polymerization. These polymers, combined with the two different PGB substrate types, allowed the evaluation of the usefulness of random versus chain‐end grafting in producing arborescent copolymers useful as unimolecular micelles in organic and aqueous media. Size exclusion chromatography served to determine the grafting yield, molar mass, dispersity, and branching functionality of the copolymers. Dynamic light scattering measurements provided information on their aggregation behavior in aqueous environments. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 1197–1209  相似文献   
220.
A two step efficient and practical synthesis of a variety of 4-chromanones is described. Phenols undergo a Michael addition to acrylonitriles in the presence of catalytic amounts of potassium carbonate and tert-butanol to generate the corresponding 3-aryloxypropanenitriles in 50-93% yields. Treatment of the resulting aryloxypropionitriles with 1.5 equiv of TfOH and 5 equiv of TFA, followed by an aqueous work up afforded 4-chromanones in moderate to excellent yields.  相似文献   
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