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101.
102.
We show that a compact complex manifold is Moishezon if and only if it carries a strictly positive, integral (1, 1)-current.
We then study holomorphic line bundles carrying singular hermitian metrics with semi-positive curvature currents, and we give
some cases in which these line bundles are big. We use these cases to provide sufficient conditions for a compact complex
manifold to be Moishezon in terms of the existence of certain semi-positive, integral (1,1)-currents. We also show that the
intersection number of two closed semi-positive currents of complementary degrees on a compact complex manifold is positive
when the intersection of their singular supports is contained in a Stein domain.
The first author was partially supported by National Science Foundation Grant Nos. DMS-8922760 and DMS-9204273. The second
author was partially supported by National Science Foundation Grant Nos. DMS-9001365 and DMS-9204037. 相似文献
103.
104.
105.
The conformational properties of the furanose ring of purine- and pyrimidine--nucleosides and-nucleotides are studied quantum-mechanically with the help of the PCILO method, using the pseudorotational concept. The computations point to the existence of two stable conformational zones centered around the C(3)-endo and C(2)-endo conformations which in the isolated furanose ring are separated by barriers of the order of 4 kcal/mole. In nucleosides one of the barriers (the one running through the O(1)-exo-C(2)-exo path) becomes very high. A detailed study is made of the relation between the phase angle of pseudorotation, P, and the torsion angle about the glycosyl bond,
CN. A very satisfactory agreement with the available experimental data is observed.
This research was supported by the R.C.P. 173 and the A.T.P. A 655-2303 of the C.N.R.S. 相似文献
Zusammenfassung Die Konformationseigenschaften des Furanoserings in -Nucleosiden und Nucleotiden von Purin und Pyrimidin werden nach der PCILO-Methode unter Berücksichtigung der pseudorotatorischen Betrachtungsweise studiert. Die Rechnung läßt auf die Existenz zweier stabiler Konformationszonen schließen, die in der Umgebung der C(2)-endo und der C(3)-endo Konformationen liegen, und die im isolierten Furanosering durch Energiebarrieren der Größenordnung von 4 kcal/mol voneinander getrennt sind. In Nucleosiden wird eine der Barrieren (die durch den Weg O(1)-exo-C(2)-exo gekennzeichnete) sehr hoch. Die Relation zwischen dem Phasenwinkel der Pseudorotation, P, und dem Drehwinkel um die Glycosylbindung, CN, wird einer eingehenden Untersuchung unterworfen. Man beobachtet eine sehr zufriedenstellende Übereinstimmung mit den verfügbaren experimentellen Daten.
Résumé Les propriétés conformationnelles du noyau furanose des -nucleosides et nucleotides des purines et pyrimidines sont étudiées par la méthode PCILO en faisant appel au concept de la pseudorotation. Les calculs indiquent l'existence de deux zones de conformations stables, centrées autour des conformations C(2)-endo et C(3)-endo, qui sont dans le sucre isolé séparées par des barrières de l'ordre de 4 kcal/mole. Dans les nucleosides, l'une de ces barrières (celle qui passe par le chemin O(1)-exo-C(2)-exo) devient très élevée. Une étude détaillée est effectuée sur la relation entre l'angle de phase de la pseudorotation P et l'angle de torsion autour de la liaison glycosylique, CN. Un excellent accord avec les données expérimentales disponibles est observé.
This research was supported by the R.C.P. 173 and the A.T.P. A 655-2303 of the C.N.R.S. 相似文献
106.
Based on the similarity in properties of arsenate and phosphate, the colorimetric method using the molybdene blue complex was tested in order to determine low As(V) concentration in waters. The influence of complex formation time, daylight, temperature and competitive anions (silicate and sulphate) upon complex formation was determined. Optimal complex formation was reached in 1 h at 20±1 °C and was slightly favoured when developed in daylight. The formation rate declined with decreasing reaction temperature and no influence of any of the competitive anions tested (at concentrations usually found in natural waters of granitic areas) was noted. The detection limit of this method was 20 μg As(V) l−1. This simple, fast and sensitive arsenic determination method is suitable for field analysis, especially for waters containing low levels of phosphate and organic matter. Through arsenate determination, this colorimetric method allowed the arsenite oxidation efficiency of five common industrial oxidants to be compared. H2O2 and MnO2(s) were not considered as effective oxidants as a high excess was necessary to ensure As(III) oxidation. NaOCl and KMnO4 were promising oxidants as they allowed complete arsenite oxidation with a small excess for NaOCl or even less than the electron stoichiometric ratio in the case of KMnO4. FeCl3 was the most effective oxidant among the reagents tested here. 相似文献
107.
Bernard Demerseman Pascale Le Coupanec Pierre H. Dixneuf 《Journal of organometallic chemistry》1985,287(3):C35-C38
13C NMR measurements were performed on [Re3(μ-H)3(CO)10]2? at various temperatures and field strengths. Selective decoupling allowed assignments of the carbonyl resonances. Spin-lattice relaxation time measurements indicated that two mechanisms, scalar coupling and chemical shielding anisotropy, contribute to the relaxation of carbon-13. Variable temperature experiments revealed that more than one mechanism is responsible for the fluxional behaviour. 相似文献
108.
Pierre Netchitaïlo Mohamed Othman Bernard Decroix 《Journal of heterocyclic chemistry》1997,34(1):321-324
2-Thienylthiomethylphthalimides 3a,b were synthesized by action of Chloromethylphthalimide on 2-or 3-mercaptothiophene. Reduction of 3a,b and Wittig reaction using carbethoxycarbonyltriphenyl-phosphorane gave the corresponding acetic acids 5a,b which cyclized under Friedel and Crafts conditions to lead the thienothiazocinoisoindolediones 6a,b. Thienothiazinoisoindolones 7a,b were obtained from hydroxyisoindolones derivatives 4a,b in acid conditions via an acyliminium ion. 相似文献
109.
110.
Francois Delyon Yves Lévy Bernard Souillard 《Communications in Mathematical Physics》1985,100(4):463-470
We prove that discrete Schrödinger operators on
d
with a random-potential have almost-surely only pure point spectrum and exponentially decaying eigenfunctions for large disorder or large energy. This is the first proof of localization for multi-dimensional Anderson models.Groupe de recherche 048 du CNRS 相似文献