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41.
Raghunathan V  Han Y  Korth O  Ge NH  Potma EO 《Optics letters》2011,36(19):3891-3893
We demonstrate rapid vibrational imaging based on sum frequency generation (SFG) microscopy with a collinear excitation geometry. Using the tunable picosecond pulses from a high-repetition-rate optical parametric oscillator, vibrationally selective imaging of collagen fibers is achieved with submicrometer lateral resolution. We furthermore show simultaneous SFG and second harmonic generation imaging to emphasize the compatibility of the microscope with other nonlinear optical modalities.  相似文献   
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Effects of changing the interparticle separation on the surface plasmon bands of ultrathin films of gold nanoparticles have been investigated by examining the interaction of alkanethiols of varying chain length on nanocrystalline gold films generated at the organic-aqueous interface. Adsorption of alkanethiols causes blue-shifts of the surface plasmon adsorption band, the magnitude of the shift being proportional to the chain length. The disordered nanocrystals thus created (lambdamax, 530 m) are in equilibrium with the ordered nanocrystals in the film (lambdamax, 700 m) as indicated by an isosbestic point around 600 nm. Long chain thiols disintegrate or disorder the gold films more effectively, as demonstrated by the increased population of the thiol-capped gold nanocrystals in solution. The rate of interaction of the thiols with the film decreases with the decreasing chain length. The effect of an alkanethiol on the spectrum of the gold film is specific, in that the effects with long and short chains are reversible. The changes in the plasmon band of gold due to interparticle separation can be satisfactorily modeled on the basis of the Maxwell-Garnett formalism. Spectroscopic studies, augmented by calorimetric measurements, suggest that the interaction of alkanethiols involves two steps, the first step being the exothermic gold film-thiol interaction and the second step includes the endothermic disordering process followed by further thiol capping of isolated gold particles.  相似文献   
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A series of trans‐2,3‐dihydrofuro[3,2‐c]coumarins ( 4 ) has been synthesized by a one‐pot multicomponent reaction by aromatic aldehydes, 4‐hydroxycoumarin, α‐tosyloxyketones, and pyridine using triethylamine as catalysts in acetonitrile. The synthesized compounds were then screened for their antioxidant and anthelmintic activities.  相似文献   
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We report the interfacial properties of monolayers of Ag nanoparticles 10-50 nm in diameter formed at the toluene-water interface under steady as well as oscillatory shear. Strain amplitude sweep measurements carried out on the film reveal a shear thickening peak in the loss moduli (G") at large amplitudes followed by a power law decay of the storage (G') and loss moduli with exponents in the ratio 2:1. In the frequency sweep measurements at low frequencies, the storage modulus remains nearly independent of the angular frequency, whereas G" reveals a power law dependence with a negative slope, a behavior reminiscent of soft glassy systems. Under steady shear, a finite yield stress is observed in the limit of shear rate .gamma going to zero. However, for .gamma > 1 s-1, the shear stress increases gradually. In addition, a significant deviation from the Cox-Merz rule confirms that the monolayer of Ag nanoparticles at the toluene-water interface forms a soft two-dimensional colloidal glass.  相似文献   
47.
Photosynthesis involves light-harvesting complexes where an array of antenna pigment channels the absorbed solar energy to the reaction centre of a photosystem. This work reports a supramolecular dendrimer-dye assembly that mimics the natural light-harvesting mechanism. A dendrimeric molecule based on two-fluorophores has been constructed with three coumarin units at the end of three long arms and a 7-diethylaminocoumarin unit at the interior. The molecule self-aggregates in water into spherical micelles, which can encapsulate a rose-bengal dye (RB). On excitation, peripheral coumarin units shuttled the energy to the loaded RB dye reaction center via a two-step cascade resonance energy transfer (RET). The energy absorbed in the periphery is funnelled efficiently, resulting in a strong emission from the dye that resembles an energy funnel. The energy transfer cascade has been studied with both steady-state and time-resolved fluorescence spectroscopy. Molecular dynamics simulations of the self-assembled aggregates in water were also in agreement with the experimental observations.  相似文献   
48.
Many heterogeneous catalysts exploit strained active layers to modulate reactivity and/or selectivity. It is therefore significant that density functional theory, as well as experimental approaches, find that tensile strain makes the gold surface more binding for oxygen, in other words, less noble. We show that this behavior does not apply when re‐structuring of the gold surface is allowed to occur simultaneously with the adsorption of oxygen. In situ cantilever‐bending studies show the surface stress to increase when oxygen species adsorb on a (111)‐textured gold surface in aqueous H2SO4. This implies a positive sign of the electrocapillary coupling parameter and, hence, a trend for weaker oxygen binding in response to tensile strain. These conflicting findings indicate that different electrosorption processes, and specifically oxygen species adsorption on the bulk‐terminated surface, exhibit fundamentally different coupling between the chemistry and the mechanics of the surface.  相似文献   
49.
We give an introduction to certain topics from functional analysis which are relevant for physics in general and in particular for quantum mechanics. Starting from some examples, we discuss the theory of Hilbert spaces, spectral theory of unbounded operators, distributions and their applications and present some facts from operator algebras. We do not give proofs, but present examples and analogies from physics which should be useful to get a feeling for the topics considered.  相似文献   
50.
We have synthesized a completely new family of acyclic trimeric cyclodiphosphazane compounds comprising NH, NiPr, NtBu and NPh bridging groups. In addition, the first NH-bridged acyclic dimeric cyclophosphazane has been produced. The trimeric species display highly tuneable characteristics so that the distance between the terminal N(H)R moieties can be readily modulated by the steric bulk present in the bridging groups (ranging from ≈6 to ≈10 Å). Moreover, these species exhibit pronounced topological changes when a weak non-bonding NH⋅⋅⋅π aryl interaction is introduced. Finally, the NH-bridged chloride binding affinities have been calculated and benchmarked along with the existing experimental data available for monomeric cyclodiphosphazanes. Our results underscore these species as promising hydrogen bond donors for supramolecular host–guest applications.  相似文献   
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