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181.
Jesús del Barrio Eva Blasco Luis Oriol Rafael Alcalá Carlos Sánchez‐Somolinos 《Journal of polymer science. Part A, Polymer chemistry》2013,51(8):1716-1725
We have demonstrated the preparation of a series of photoaddressable supramolecular block copolymers by mixing a carboxy‐terminated azobenzene derivative, 6‐[4‐(4′‐cyanophenylazo)phenyloxy]hexanoic acid (AZO), and two polystyrene‐b‐poly(4‐vinylpiridine) (PS‐b‐P4VP) block copolymers. AZO can be selectively attached to the P4VP block of PS‐b‐P4VP through hydrogen bonding interactions. The assembly of AZO with vinylpyridine group‐containing polymers was initially investigated on a model system composed of P4VP homopolymer and AZO. Homogeneous liquid crystalline materials were obtained for ratios of AZO to vinylpyridine repeating unit, x, lower or equal to 0.50. Mixtures with higher x resulted in heterogeneous materials showing clear macrophase separation. Accordingly, a series of hydrogen‐bonded complexes of PS‐b‐P4VP and AZO, PS‐b‐P4VP(AZO)x, with x = 0.25 and x = 0.50 were prepared. Lamellar and spherical morphologies were observed for the complexes based on PS24‐b‐P4VP9.5 (Mn,PS = 24,000, Mn,P4VP = 9500) and PS24‐b‐P4VP1.9 (Mn,PS = 24,000, Mn,P4VP = 1900), respectively. Photoinduced orientation of the azobenzene units was obtained in films of P4VP(AZO)x and PS‐b‐P4VP(AZO)x with x = 0.25 and 0.50 by using 488 nm linearly polarized light and characterized through birefringence and dichroism measurements. This investigation shows a versatile and less laborious approach to azobenzene‐containing polymer materials with low chromophore content, of interest in optical application. © 2013 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献
182.
Michaela Wilhelm Eva Berssen Rainer Koch Henry Strasdeit 《Monatshefte für Chemie / Chemical Monthly》2002,133(8):1097-1108
Summary. Lipoyl imidazolide reacts with aza-15-crown-5 (1,4,7,10-tetraoxa-13-azacyclopentadecane) or aza-18-crown-6 (1,4,7,10,13-pentaoxa-16-azacyclooctadecane)
to afford new N-lipoylated azacrown compounds in good yields. These compounds can be transformed into 1,3-dithiols and amines by reduction
with complex hydrides of the disulfide and/or amide group of the lipoyl chain. The new pendant-arm macrocycles react as heteroditopic
ligands by forming dithiolate and disulfide complexes with the ‘soft’ metal ions Ni2+ and Pd2+, respectively, and an amine complex with the ‘hard’ Li+ ion. Semiempirical and DFT calculations on the complexation of a lithium ion give a most favourable structure in which the
azacrown and two solvent molecules are in contact with the metal but not the pendant arm.
Received January 29, 2002; accepted (revised) March 25, 2002 相似文献
183.
Eva M. Mazcuñán-Navarro 《Journal of Mathematical Analysis and Applications》2008,337(1):197-218
In this paper we establish lower bounds for the weakly convergent sequence coefficient WCS(X) of a Banach space X, in terms of some well known moduli and coefficients. By mean of these bounds we identify several properties, of geometrical nature, which imply normal structure. We show that these properties are strictly more general than other previously known sufficient conditions for normal structure. 相似文献
184.
185.
Victor Guillemin Eva Miranda Ana Rita Pires 《Bulletin of the Brazilian Mathematical Society》2011,42(4):607-623
In this short note we give a complete characterization of a certain class of compact corank one Poisson manifolds, those equipped with a closed one-form defining the symplectic foliation and a closed two-form extending the symplectic form on each leaf. If such a manifold has a compact leaf, then all the leaves are compact, and furthermore the manifold is a mapping torus of a compact leaf. These manifolds and their regular Poisson structures admit an extension as the critical hypersurface of a b-Poisson manifold as we will see in [9]. 相似文献
186.
187.
188.
Edmund Knecht und Eva Hibbert 《Fresenius' Journal of Analytical Chemistry》1908,47(6-7):425-426
Ohne Zusammenfassung 相似文献
189.
Eva Raluy Oscar Pàmies Montserrat Diéguez Stephane Rosset Alexander Alexakis 《Tetrahedron: Asymmetry》2009,20(16):1930-1935
A sugar-based phosphite–phosphoroamidite and diphosphoroamidite ligand library L1–L5a–g was tested in the asymmetric Cu-catalyzed 1,4-conjugate addition reactions of β-substituted and β,β′-disubstituted enones. Our results indicated that the selectivity was strongly dependent on the ligand parameters and on the substrate structure. Moderate-to-good enantioselectivities (ees up to 84%) were obtained in the 1,4-addition of several types of β-substituted cyclic and linear substrates. Of particular note is the high enantioselectivity (ees up to 90%) obtained for the more challenging β,β′-disubstituted 3-methyl-cyclohexenone. 相似文献
190.
G. Buogo P. Meduri W. Lintzel Eva Herring W. P. Golmow und F. Hillig 《Fresenius' Journal of Analytical Chemistry》1943,125(7-8):309-310
Ohne Zusammenfassung 相似文献