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Vincenzo Recupero 《Mathematical Methods in the Applied Sciences》2008,31(11):1283-1295
The vector play operator is the solution operator of a class of evolution variational inequalities arising in continuum mechanics. For regular data, the existence of solutions is easily obtained from general results on maximal monotone operators. If the datum is a continuous function of bounded variation, then the existence of a weak solution is usually proved by means of a time discretization procedure. In this paper we give a short proof of the existence of the play operator on rectifiable curves making use of basic facts of measure theory. We also drop the separability assumptions usually made by other authors. Copyright © 2007 John Wiley & Sons, Ltd. 相似文献
125.
Dr. Irene Vassalini Dr. Laura Borgese Michele Mariz Prof. Stefano Polizzi Dr. Giuliana Aquilanti Prof. Paolo Ghigna Prof. Andrea Sartorel Prof. Vincenzo Amendola Prof. Ivano Alessandri 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2017,129(23):6689-6693
Oxygen evolution reaction (OER) is the most critical step in water splitting, still limiting the development of efficient alkaline water electrolyzers. Here we investigate the OER activity of Au–Fe nanoalloys obtained by laser-ablation synthesis in solution. This method allows a high amount of iron (up to 11 at %) to be incorporated into the gold lattice, which is not possible in Au–Fe alloys synthesized by other routes, due to thermodynamic constraints. The Au0.89Fe0.11 nanoalloys exhibit strongly enhanced OER in comparison to the individual pure metal nanoparticles, lowering the onset of OER and increasing up to 20 times the current density in alkaline aqueous solutions. Such a remarkable electrocatalytic activity is associated to nanoalloying, as demonstrated by comparative examples with physical mixtures of gold and iron nanoparticles. These results open attractive scenarios to the use of kinetically stable nanoalloys for catalysis and energy conversion. 相似文献
126.
Ranieri A Monari S Sola M Borsari M Battistuzzi G Ringhieri P Nastri F Pavone V Lombardi A 《Langmuir : the ACS journal of surfaces and colloids》2010,26(23):17831-17835
Mimochrome VI (MC-VI) is a synthetic heme peptide containing a helix-heme-helix sandwich motif designed to reproduce the catalytic activity of heme oxidases. The thermodynamics of Fe(III) to Fe(II) reduction and the kinetics of the electron-transfer process for MC-VI immobilized through hydrophobic interactions on a gold electrode coated with a nonpolar SAM of decane-1-thiol have been determined through cyclic voltammetry. Immobilization slightly affects the reduction potential of MC-VI, which under these conditions electrocatalytically turns over molecular oxygen. This work sets the premise for the exploitation of totally synthetic mimochrome-modified electrode surfaces for clinical and pharmaceutical biosensing. 相似文献
127.
The enantioselective synthesis of 3(S)-hydroxy polygodial and its acetyl derivative is described. The construction of the 3-hydroxy drimane skeleton was based on the titanium-catalyzed radical cyclization of (10S)-10, 11-epoxy-farnesyl acetate. Only underivatized 3(S)-hydroxy polygodial showed activity in assays on VR1 vanilloid receptor in HEK cells transfected with the human VR1. 相似文献
128.
Muhammad NajeebUllah David W. Knight Munawar Ali Munawar Fusillo Vincenzo 《Tetrahedron》2010,66(34):6761-2710
A convenient and efficient method for the synthesis of triphenodioxazines [TPDOs] 1 by oxidative cyclisation of 2,5-bis-(arylamino)-3,6-dichlorocyclohexa-2,5-diene-1,4-diones 6 using potassium persulfate as the oxidising agent in 95?97% sulfuric acid triggered by microwave irradiation is described. 相似文献
129.
Giorgia Oliviero Nicola Borbone Vincenzo Piccialli Gennaro Piccialli Luciano Mayol 《Tetrahedron》2010,66(10):1931-6144
We report here an efficient solid-phase synthesis of N-1-alkyl-substituted analogues of cyclic inosine-diphosphate-ribose (cIDPR), a mimic of cyclic ADP-ribose (cADPR). Our synthetic strategy makes use of a polystyrene support to which inosine was bonded through a 2′,3′-acetal linkage. Insertion of a ω-hydroxy-polymethylene chain of variable length on N-1, followed by conversion into N-1-alkylinosine-bis-phosphate derivatives and cyclization, allowed to obtain analogues of cIDPR of various ring size. The cyclization step was carried out both in solid-phase and in solution by pyrophosphate bond formation. The effect of the N-1-polymethylene chain length on the cyclization yields as well as the reaction conditions, which led to the solid-phase pyrophosphate bond formation, were thoroughly investigated. 相似文献
130.
Vincenzo Benessere Raffaella Del Litto Antonella De Roma Francesco Ruffo 《Coordination chemistry reviews》2010,254(5-6):390-401
“Privileged ligands” are chiral auxiliaries of wide applicability in asymmetric catalysis. In the previous decades, their effective three-dimensional structures have often been reproduced by using building blocks from a “chiral pool”, such as the carbohydrates. This strategy has provided unique ligand moieties which combine the performance of “privileged ligands” with increased flexibility and accessibility. This review gives an overview of the research within this field, giving emphasis to the best results obtained with each ligand type. 相似文献