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301.
Simone Zanella Dr. Michele Mingozzi Alberto Dal Corso Dr. Roberto Fanelli Dr. Daniela Arosio Prof. Dr. Marco Cosentino Dr. Laura Schembri Dr. Franca Marino Dr. Marta De Zotti Prof. Dr. Fernando Formaggio Dr. Luca Pignataro Prof. Dr. Laura Belvisi Prof. Dr. Umberto Piarulli Prof. Dr. Cesare Gennari 《ChemistryOpen》2015,4(5):633-641
A dual-action ligand targeting both integrin αVβ3 and vascular endothelial growth factor receptors (VEGFRs), was synthesized via conjugation of a cyclic peptidomimetic αVβ3 Arg-Gly-Asp (RGD) ligand with a decapentapeptide. The latter was obtained from a known VEGFR antagonist by acetylation at the Lys13 side chain. Functionalization of the precursor ligands was carried out in solution and in the solid phase, affording two fragments: an alkyne VEGFR ligand and the azide integrin αVβ3 ligand, which were conjugated by click chemistry. Circular dichroism studies confirmed that both the RGD and VEGFR ligand portions of the dual-action compound substantially adopt the biologically active conformation. In vitro binding assays on isolated integrin αVβ3 and VEGFR-1 showed that the dual-action conjugate retains a good level of affinity for both its target receptors, although with one order of magnitude (10/20 times) decrease in potency. The dual-action ligand strongly inhibited the VEGF-induced morphogenesis in Human Umbilical Vein Endothelial Cells (HUVECs). Remarkably, its efficiency in preventing the formation of new blood vessels was similar to that of the original individual ligands, despite the worse affinity towards integrin αVβ3 and VEGFR-1. 相似文献
302.
303.
Catalytic Asymmetric Reactions of 4‐Substituted Indoles with Nitroethene: A Direct Entry to Ergot Alkaloid Structures 下载免费PDF全文
Simone Romanini Emilio Galletti Dr. Lorenzo Caruana Prof. Andrea Mazzanti Prof. Fahmi Himo Dr. Stefano Santoro Prof. Mariafrancesca Fochi Prof. Luca Bernardi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(49):17578-17582
A domino Friedel–Crafts/nitro‐Michael reaction between 4‐substituted indoles and nitroethene is presented. The reaction is catalyzed by BINOL‐derived phosphoric acid catalysts, and delivers the corresponding 3,4‐ring‐fused indoles with very good results in terms of yields and diastereo‐ and enantioselectivities. The tricyclic benzo[cd]indole products bear a nitro group at the right position to serve as precursors of ergot alkaloids, as demonstrated by the formal synthesis of 6,7‐secoagroclavine from one of the adducts. DFT calculations suggest that the outcome of the reaction stems from the preferential evolution of a key nitronic acid intermediate through a nucleophilic addition pathway, rather than to the expected “quenching” through protonation. 相似文献
304.
The Cage Structure of IndanCHF3 is Based on the Cooperative Effects of CH⋅⋅⋅π and CH⋅⋅⋅F Weak Hydrogen Bonds 下载免费PDF全文
Dr. Laura B. Favero Weixing Li Lorenzo Spada Dr. Luca Evangelisti Giorgio Visentin Prof. Dr. Walther Caminati 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(45):15970-15973
The structural and energetic features of the C?H???π interaction and the internal dynamics of the CHF3 group change drastically in going from benzene?CHF3 to indan?CHF3, according to the analysis of the rotational spectrum of the latter complex generated in a supersonic expansion. 相似文献
305.
We compare different notions of curvature on contact sub-Riemannian manifolds. In particular, we introduce canonical curvatures as the coefficients of the sub-Riemannian Jacobi equation. The main result is that all these coefficients are encoded in the asymptotic expansion of the horizontal derivatives of the sub-Riemannian distance. We explicitly compute their expressions in terms of the standard tensors of contact geometry. As an application of these results, we obtain a sub-Riemannian version of the Bonnet–Myers theorem that applies to any contact manifold. 相似文献
306.
Anirudra Parajuli Daniel H. Kwak Luca Dalponte Dr. Niina Leikoski Tomas Galica Ugochukwu Umeobika Dr. Laurent Trembleau Andrew Bent Prof. Kaarina Sivonen Matti Wahlsten Dr. Hao Wang Dr. Ermanno Rizzi Prof. Gianluca De Bellis Prof. James Naismith Prof. Marcel Jaspars Prof. Xinyu Liu Dr. Wael Houssen Dr. David Peter Fewer 《Angewandte Chemie (International ed. in English)》2017,56(2):433-433
307.
308.
Roberto?Alicandro Lucia?De?Luca Adriana?Garroni Marcello?PonsiglioneEmail author 《Calculus of Variations and Partial Differential Equations》2017,56(5):148
In Alicandro et al. (J Mech Phys Solids 92:87–104, 2016) a simple discrete scheme for the motion of screw dislocations toward low energy configurations has been proposed. There, a formal limit of such a scheme, as the lattice spacing and the time step tend to zero, has been described. The limiting dynamics agrees with the maximal dissipation criterion introduced in Cermelli and Gurtin (Arch Ration Mech Anal 148, 1999) and predicts motion along the glide directions of the crystal. In this paper, we provide rigorous proofs of the results in [3], and in particular of the passage from the discrete to the continuous dynamics. The proofs are based on \(\Gamma \)-convergence techniques. 相似文献
309.
In this paper, the rheological properties of an extrudable cement-based paste are investigated by means of an original ram
extrusion apparatus (capillary rheometer). The experimental results indicate that a careful measurement of the die pressure
is necessary to obtain a realistic viscosity vs shear rate curve, as required in extrusion technology. In particular, it is
shown that the optimal test configuration is when the pressure measurement is made directly inside the rheometer die. By applying
this rheological methodology in steady-state conditions, it has been observed that the extrudable cement-based material here
evaluated obeys to a simple power–law equation, in the range of shear rates investigated, which are suitable for an industrial
extrusion process.
This paper was presented at the third Annual European Rheology Conference (AERC) held in Hersonissos, Crete, Greece, April
24–27, 2006. 相似文献
310.
Two definitions of free energy for a linear viscoelastic material, due to Graffi and to Coleman and Owen, are considered, and the compatibility of these definitions with some expressions of the free energy proposed in the literature is examined. For the expressions of Staverman and Schwarzl and of Breuer and Onat, the two definitions are proved to be equivalent, and the set of all relaxation functions for which the two expressions are indeed free energies is determined. Two more expressions, proposed by Volterra and Graffi and by Morro and Vianello, are taken into consideration. For them, only the classes of relaxation functions for which they are free energies according to the first definition, is completely characterized. All results are established under regularity assumptions weaker than those usually made in the literature. 相似文献