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271.
Campos JM Sánchez-Martín RM Cruz-López O Conejo-García A Gallo MA Espinosa A 《Magnetic resonance in chemistry : MRC》2005,43(12):1066-1071
1H and 13C NMR spectroscopic data of both the quinolinium ring and the spacers for 32 symmetrical bisquinolinium compounds were assigned by a combination of one- and two-dimensional experiments (DEPT, HMBC, HMQC). The compounds have electron-releasing groups at position 4 of the quinolinium ring, with several arylalkyl linkers such as the 3,3'-, 4,4'-bis(methylene)biphenyl and 4,4'-bis(methylene)bibenzyl moieties. 相似文献
272.
We provide an adjustment factor for ablation algorithms used in photorefractive laser surgery that takes into account how laser polarization in reflection losses affects the cornea. We evaluate the influence of this factor on corneal radius and asphericity after surgery, showing that it is significant for visual performance (effective visual acuity is reduced) and for the correction of eye aberrations. Our data indicate that this adjustment factor should be included in the ablation algorithms (depending on the polarization state of each laser device) that are proposed for customized corneal ablation, which need great accuracy for minimization of eye aberrations. 相似文献
273.
Non-Abelian holonomies can be generated and detected in certain superconducting nanocircuits. Here we consider an example where the non-Abelian operations are related to the adiabatic charge dynamics of the Josephson network. We demonstrate that such a device can be applied both for adiabatic charge pumping and as an implementation of a quantum computer. 相似文献
274.
M.Luz Gallego Mercedes Cano JosA. Campo JosV. Heras Elena Pinilla M.Rosario Torres 《Helvetica chimica acta》2005,88(9):2433-2440
The structures of [Pd(η3‐C3H5)(HpzR2)2](BF4) (HpzR2=Hpzbp2=3,5‐bis(4‐butoxyphenyl)‐1H‐pyrazole, 1 ; HpzR2=HpzNO2=3,5‐dimethyl‐4‐nitro‐1H‐pyrazole=Hdmnpz, 2 ) and [Ag(HpzR2)2](A) (HpzR2=Hpzbp2, A= , 3 ; HpzR2=HpzNO2, A= , 4 ) were comparatively analyzed to determine the factors responsible for polymeric assemblies. In all cases, the H‐bonding interactions between the pyrazole moieties and the appropriate counterion and, in particular, the orientation of the NH groups of the pyrazole ligands are determinant of one‐dimensional polymeric arrays. In this context, the new compound [Ag(HpzNO2)2](NO3) ( 5 ) was synthesized and its structure analyzed by X‐ray diffraction (Fig. 4). The HpzNO2 serves as N‐monodentate ligand, which coordinates to the AgI center through its pyrazole N‐atom giving rise to an almost linear N Ag N geometry. The planar NO counterion bridges two adjacent AgI centers to form a one‐dimensional zigzag‐shaped chain which is also supported by the presence of N H⋅⋅⋅O bonds between the pyrazole NH group of adjacent cationic entities and the remaining O‐atom of the bridging NO (Fig. 5). The chains are further extended to a two‐dimensional layer‐like structure through additional Ag⋅⋅⋅O interactions involving the NO2 substituents at the pyrazole ligands (Fig. 6). 相似文献
275.
276.
Palumbo O Cantelli R Paolone A Jensen CM Srinivasan SS 《The journal of physical chemistry. B》2005,109(3):1168-1173
We report the first measurements of elastic modulus and energy dissipation in Ti-doped and undoped sodium aluminum hydride. It is shown that the chemical reactions that occur by varying the sample temperatures or by aging most sensitively affect the elastic constants, such that the modulus variations allow the time and temperature evolution of decomposition to be monitored. After a well-defined thermal treatment at 436 K, a thermally activated relaxation process appears at 70 K in the kilohertz range, denoting the existence of a new species, likely involving hydrogen, having a very high mobility, that is, 10(3) jumps/s at the peak temperature corresponding to a relaxation rate of about 10(11) s(-1) at room temperature. The activation energy of the process is 0.126 eV and the preexponential factor 7 x 10(-14) s, which is typical of point defect relaxation. The peak is very broad with respect to a single Debye process, indicating strong interaction or/and multiple jumping type of the mobile entity. The present data suggest that the models aiming at interpreting the decomposition reactions and kinetics should take into account the indicated point-defect dynamics and stoichiometry defects. 相似文献
277.
Rosario Strano 《Annali di Matematica Pura ed Applicata》1979,121(1):157-169
Sunto Dati uno schema X e un suo sottosistema aperto U⊂X, si studiano alcune condizioni affinchè l'omomorfismo canonicoBr(X)→Br(U) fra i relativi gruppi di Brauer sia iniettivo o suriettivo.
Entrata in Redazione l'8 febbraio 1978.
Lavoro eseguito nell'ambito della sezione n. 3 del G.N.S.A.G.A. 相似文献
278.
Experimental results on the nuclear spin-lattice and nuclear spin-spin relaxation times in the ferromagnetic EuB6 at temperatures below 4·2 K are presented using the external magnetic field,H
ext, in the range of 0 ⩽H
ext ⩽ 10 kG. Nuclear spin-spin relaxation time computed on the basis of the Suhl-Nakamura process turns out to be 3·2μs, which compares well with the experimental value 11·1μs obtained with the 10 kG magnetic field at 1·7 K. It is found that in the ferromagnetic EuB6,T
1 is approximately 5 × 103 times larger thanT
2 at 1·7 K with the 10 kG magnetic field. Thus the effect ofT
1 onT
2 can be neglected. From the experimental value ofT
2, the value of the homogeneous line broadening is found to be 14 kHz. The corresponding value obtained from the cw method
is 175 kHz. This evidently shows the presence of the inhomogeneous line broadening in the cw NMR. 相似文献
279.
Martín-Zamora E Ferrete A Llera JM Muñoz JM Pappalardo RR Fernández R Lassaletta JM 《Chemistry (Weinheim an der Bergstrasse, Germany)》2004,10(23):6111-6129
Staudinger-like cycloadditions between chiral, non-racemic N,N-dialkylhydrazones 1 and functionalized ketenes constitute an efficient methodology for the stereoselective construction of the beta-lactam ring. The potential for fine tuning of the dialkylamino auxiliary structure, the availability of a high-yielding deprotection method for the release of the free azetidinones, and the high thermal and chemical stability of hydrazones as N-dialkylamino imines are highlighted as the key elements for the success of the strategy. This last aspect is of particular importance concerning generality: even hydrazones from easily enolizable aldehydes or from formaldehyde reacted to afford the corresponding cycloadducts with high chemical and stereochemical yields. The syntheses of the beta-amino-alpha-hydroxyacids (2R,3S)-phenylisoserine (42) and (2R,3S)-norstatin (45) were accomplished as illustrative examples of the synthetic utility of this procedure. A model system for the cycloaddition of g series auxiliaries was studied by ab initio computational methods. The collected results support a two-step mechanism through zwitterionic intermediates, and explain the observed absolute and relative stereochemistry in terms of the preferred outward cycloaddition to the Re face of the hydrazone. 相似文献
280.
(2,6-Dichlorophenyl)- and (2,6-dibromophenyl)trialkylsilanes undergo hydrogen/metal interconversion preferentially at the 4- rather than 3-position. However, the organometallic species generated by such a "meta metalation" are thermodynamically less stable (i.e., more basic) than those that would result from an ordinary "ortho metalation". This was demonstrated by equilibration experiments based on permutational halogen/metal interconversion. A new buttressing effect can explain the unprecedented regioselectivity. It is supported by X-ray structures that reveal marked deformations of the benzene ring in halophenylsilanes. [structure: see text] 相似文献