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41.
We have developed an effective organometallic‐based procedure allowing the employment of 2‐methylphenols as easily available starting materials in the synthesis of 3‐alkylbenzofuran‐2(3H)‐ones. The first step of this protocol, an anionic homologous Fries‐rearrangement, afforded 2‐(2‐ tert ‐butyldimethylsilyloxyaryl)acetamides, which were selectively metalated and monoalkylated at the benzylic position. Acidic work‐up of crude products afforded the desired heterocycles in satisfactory overall yields. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
42.
Ugo Morin 《Annali di Matematica Pura ed Applicata》1940,19(1):257-288
Sunto. Si assegnano i tipi cremonianamente distinti di sistemi lineari completi, semplici, irriducibili di superficie algebriche
dello spazioS
3 a curva-caratteristica (variabile) di genereπ=2. Questi si distribuiscono in25 famiglie, delle quali si danno la dimensione, l'ordine minimo, ecc. e la rappresentazione analitica. 相似文献
43.
The synthesis and the phase behaviour of a homologous series of copper, bis[N-[[4-[4-(alkoxy)benzoyloxy],2-hydroxyphenyl]methylene]-methanamino] complexes is reported. They all exhibit thermotropic mesomorphism. The thermal stability range of the mesophase decreases slightly with increasing length of the alkoxy terminals. With the onset of smectic mesomorphism, for alkoxy groups containing ten carbon atoms, the stability interval of the nematic phase decreases progressively so that the compound containing 14 carbon atoms in the alkoxy terminal chains exhibits only smectic mesomorphism. Optical texture analysis suggests the smectic C nature of the phase in all cases. The enthalpies for the liquid crystal-isotropic transition have been measured and they are comparatively low. Remarkably low values have also been measured for the melting enthalpies of the smectogenic members of the series. These are associated with solid phase polymorphism which is discussed briefly. 相似文献
44.
45.
46.
We study the role of entanglement and non-locality in quantum protocols that make use of systems of identical particles. Unlike in the case of distinguishable particles, the notions of entanglement and non-locality for systems whose constituents cannot be distinguished and singly addressed are still debated. We clarify why the only approach that avoids incongruities and paradoxes is the one based on the second quantization formalism, whereby it is the entanglement of the modes that can be populated by the particles that really matters and not the particles themselves. Indeed, by means of a metrological and of a teleportation protocol, we show that inconsistencies arise in formulations that force entanglement and non-locality to be properties of the identical particles rather than of the modes they can occupy. The reason resides in the fact that orthogonal modes can always be addressed while identical particles cannot. 相似文献
47.
Vapour–liquid equilibria and densities for the ternary system chloroform + tetrahydrofuran + cyclohexane and for the binary mixtures containing chloroform have been determined at 298.15 K. Vapour–liquid equilibrium data have been collected by head-space gas-chromatographic analysis of the vapour phase directly withdrawn from an equilibration apparatus. Density measurements have been carried out by means of a vibrating tube densimeter. Molar excess Gibbs energies GE and volumes VE, as well as activity coefficients and apparent molar volumes of the components, have been obtained from the measured quantities and discussed. The binary chloroform + tetrahydrofuran displays negative deviations from ideality, while chloroform + cyclohexane positive deviations, for both volume and Gibbs energy. The GE's and VE's for the ternary system are positive in the region rich in cyclohexane while negative in the region rich in chloroform + tetrahydrofuran. This indicates that hydrogen bonding between chloroform and tetrahydrofuran molecules produces negative values of GE and VE and strongly influences the behaviour of the ternary system. 相似文献
48.
Francesca Tessore Dr. Elena Cariati Prof. Franco Cariati Prof. Dominique Roberto Prof. Renato Ugo Prof. Patrizia Mussini Prof. Cristiano Zuccaccia Dr. Alceo Macchioni Prof. 《Chemphyschem》2010,11(2):495-507
A series of 4‐X‐1‐methylpyridinium cationic nonlinear optical (NLO) chromophores (X=(E)‐CH?CHC6H5; (E)‐CH?CHC6H4‐4′‐C(CH3)3; (E)‐CH?CHC6H4‐4′‐N(CH3)2; (E)‐CH?CHC6H4‐4′‐N(C4H9)2; (E,E)‐(CH?CH)2C6H4‐4′‐N(CH3)2) with various organic (CF3SO3?, p‐CH3C6H4SO3?), inorganic (I?, ClO4?, SCN?, [Hg2I6]2?) and organometallic (cis‐[Ir(CO)2I2]?) counter anions are studied with the aim of investigating the role of ion pairing and of ionic dissociation or aggregation of ion pairs in controlling their second‐order NLO response in anhydrous chloroform solution. The combined use of electronic absorption spectra, conductimetric measurements and pulsed field gradient spin echo (PGSE) NMR experiments show that the second‐order NLO response, investigated by the electric‐field‐induced second harmonic generation (EFISH) technique, of the salts of the cationic NLO chromophores strongly depends upon the nature of the counter anion and concentration. The ion pairs are the major species at concentration around 10?3 M , and their dipole moments were determined. Generally, below 5×10?4 M , ion pairs start to dissociate into ions with parallel increase of the second‐order NLO response, due to the increased concentration of purely cationic NLO chromophores with improved NLO response. At concentration higher than 10?3 M , some multipolar aggregates, probably of H type, are formed, with parallel slight decrease of the second‐order NLO response. Ion pairing is dependent upon the nature of the counter anion and on the electronic structure of the cationic NLO chromophore. It is very strong for the thiocyanate anion in particular and, albeit to a lesser extent, for the sulfonated anions. The latter show increased tendency to self‐aggregate. 相似文献
49.
Fabio Gosetti Ugo Chiuminatto Davide Zampieri Eleonora Mazzucco Emilio Marengo Maria Carla Gennaro 《Journal of chromatography. A》2010,1217(20):3427-3434
The study investigates the natural photodegradation pathway of mono-chloroanilines in river waters, with the aim to identify the predominant photoproducts formed. At this purpose a new sensitive on-line SPE HPLC–MS/MS method has been developed with LOQ values equal or lower than the legal threshold concentration levels allowed for mono-chloroanilines in waters. The degradation processes of o-, m- and p-chloroaniline have been investigated subjecting their solutions, prepared both in ultrapure and in river water, to sun light irradiation simulated by a solar box system. The SPE HPLC–MS/MS methodology allowed to evaluate the degradation kinetics, to identify the predominant photodegradation products and to propose the chemical structures. Two photoproducts (aniline and 3-aminophenol), for which standards are available, have also been quantified. 相似文献
50.
We provide a rigorous discussion of the dipole field model which significantly improves previous treatments and clarifies the general mathematical properties of the model as a prototype of four-dimensional QFT with confining infrared singularity. By exploiting the Krein-Hilbert structure associated with the local and covariant quantization of the model, we can characterize, in a simple way, the possible physical interpretation, prove that the breaking of spacetime translation is inevitable in the physical space (mechanisms of confinement), identify a nontrivial physical vacuum sector, and discuss the breaking of symmetries and the existence and role of translationally invariant field operators, etc. 相似文献