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81.
A systematic investigation of13CD3OH infrared transitions around CO2 laser line emissions is performed by means of optoacoustic detection. Using a waveguide CO2 laser of 290 MHz tunability and, in some cases, an acoustooptic modulator to provide an extension of 180 MHz, 108 transitions are observed. Measurements of pump off-set and relative intensity have been performed. The data may be compared with those previously reported of high resolution Fourier Transform spectroscopy.Work supported by: FAPESP, CNPq, FAEP — Brasil CNR — ItaliaPermanent address: Depto de Ciências, FEIS-UNESP (15378) I.Solteira-SP, Brasil  相似文献   
82.
Summary We present noise measurements made at temperatures down to 200 mK on a tunnel junction d.c. SQUID, to be used as amplifier for the gravitational-wave experiment Nautilus of the Rome group. We find that the flux noise decreases with temperature, as expected, with a best measured value of at 0.2 K. The presence of an excess noise term independent of temperature is discussed.  相似文献   
83.
Abstract

Two new mixed-valence iron complexes with 2-pyridyl oximes, [Fe(mpko)3Fe(H2O)2(NO3)](NO3)·2H2O (1) (mpko? = methyl(2-pyridyl)ketone oximate) and [{Fe(dpko)3}2Fe](ClO4)·4H2O (2) (dpko? = bis(2-pyridyl)ketone oximate), have been prepared by reaction of FeIII with mpkoH in methanol (1) and FeII with dpkoH in methanol/water (2). Dinuclear FeII(low-spin)FeIII(high-spin) and trinuclear FeII(low-spin)FeIII(high-spin)FeII(low-spin) cations are present in the crystal structure of 1 and 2, respectively. Intermolecular hydrogen bonds in 1 lead to weak antiferromagnetic interactions between pairs of neighboring FeIII centers, which allows observation of single-ion zero-field splitting effects.  相似文献   
84.
The gram‐scale synthesis, stabilization, and characterization of well‐defined ultrasmall subnanometric catalytic clusters on solids is a challenge. The chemical synthesis and X‐ray snapshots of Pt02 clusters, homogenously distributed and densely packaged within the channels of a metal–organic framework, is presented. This hybrid material catalyzes efficiently, and even more importantly from an economic and environmental viewpoint, at low temperature (25 to 140 °C), energetically costly industrial reactions in the gas phase such as HCN production, CO2 methanation, and alkene hydrogenations. These results open the way for the design of precisely defined catalytically active ultrasmall metal clusters in solids for technically easier, cheaper, and dramatically less‐dangerous industrial reactions.  相似文献   
85.
Donatella Banti 《Tetrahedron》2004,60(37):8043-8052
Norbornene derivatives bearing endo-substituents in the 5- and 6-positions were studied as substrates for ene-yne metathesis cascades. Substrates which contained an internal alkyne and a terminal alkene or alkyne in each sidechain were found to undergo a metathesis cascade leading to pentacyclic bis-dienes and bis-trienes. Attempts to extend the chemistry further to sidechains containing two internal alkynes or two internal alkynes and a terminal alkene were not successful with the first generation Grubbs' catalyst. However, the substrate containing two internal alkynes did react with the second generation Grubbs' catalyst to give a tetra-diene containing product.  相似文献   
86.
The water soluble Ni(II) complexes of the cyclam derivatives with 1,3-benzodioxole and 1,2,3-trimethoxybenzene display the fluorescent emission typical of the covalently linked fluorophores, which results from a charge transfer excited state. On oxidation to Ni(III), the fluorescence is completely quenched due to the occurrence of an electron transfer (eT) process from the excited fluorogenic fragment Fl to the oxidized metal. Thus, fluorescence can be switched off/on at will, for several cycles, by consecutively oxidizing and reducing the metal center, in controlled potential electrolysis experiments both in acetonitrile and in aqueous 0.1 M HClO4. Occurrence of an eT process from Fl to Ni(III) ultimately depends upon the easy oxidation of Fl to Fl+, whereas failure of the occurrence of an eT process from Ni(II) to Fl has to be ascribed to the particular resistance of Fl fragments to the reduction.  相似文献   
87.
The crystal structure of (C6H5)3SnCH2CHCH2 has been determined. The asymmetric unit consists of two molecules of triphenylallyltin having virtually the same conformation. Their geometrical parameters exclude pπ-dπ bonding between the metal and the allyl double bond, and seem to be in a better agreement with a σ-π conjugation effect.  相似文献   
88.
β-(2-Aminophenyl)-α,β-ynones readily react with nitrogen nucleophiles to give three major types of products, depending on reaction conditions and variation in the nucleophiles. The reaction may lead to simple 1,2-nucleophilic adducts or, at higher temperatures, to a divergent sequential cyclisation giving rise to 2-aryl-4-aminoquinolines by reaction with amines, or to substituted 2-aryl or 2-alkyl-4-alkylidene quinazolines by reaction with amidines. The latter could also be synthesised by reaction of β-(2-aminophenyl)-α,β-ynones with iminochlorides.  相似文献   
89.
The CD3OH molecule has been investigated for new far-infrared laser lines by optically pumping with a cw waveguide CO2 laser. The increased tunability (300 MHz) with respect to a conventional CO2 laser permits to pump many new CD3OH lines. As a consequence 108 new laser lines have been discovered, ranging from 42.9 to 1155 m in wavelength. On some lines the effect of an electric Stark field has been investigated demonstrating a laser frequency tuning. The total number of known FIR laser lines from CD3OH is increased to about 340 making this molecule the most prolific together with CH3OH.  相似文献   
90.
The work performed by our research group during the last few years in the area of bioerodible-biodegradable polymers as designed to the formulation of systems for the controlled delivery of drugs and as specific sorbents of uraemic toxins is broadly reviewed. In particular, attention has been focused on the strategies adopted in the preparation of functional polymers containing hydroxyl or carboxyl groups, suitable to establish specific bonding and non-bonding interactions with conventional and proteic drugs.  相似文献   
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