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101.
Summary
In this paper order-isomorphisms between subnormal structures of subsoluble groups are considered, and the images of generalized nilpotent groups in such isomorphisms are studied. A result of Pazderski about the Fitting subgroup of finite soluble groups is also extended to the upper Baer series of subsoluble groups, and an extension to infinite groups of a theorem of Heineken about isomorphisms between lattices of subnormal subgroups of finite groups is given.
Lavoro eseguito nell'ambito del G.N.S.A.G.A. del C.N.R. 相似文献
Lavoro eseguito nell'ambito del G.N.S.A.G.A. del C.N.R. 相似文献
102.
We establish some monotonicity results and inequalities involving elliptic integrals of the first and the second kind.
Work sponsored by the Ministero dell’Università e della Ricerca Scientifica e Tecnologica of Italy. 相似文献
103.
The microbial activity in a Rhodic eutrudox (R), a Typic eutrudox (V) and a Quartzipsamment (Q) was monitored by respirometric and calorimetric methods. CO2 evolution was monitored for 98 days by titrimetry and conductimetry for control amended samples (A) with 25% of cattle manure (E), municipal refuse compost (L), earthworm casts (H) or 1.25 kg ha−1 of trifluralin (T). Average values of all treatments through respiration at the end of the incubation period were 5.24±0.34, 6.13±0.31 and 6.50±0.33, in mg CO2 g−1 soil, for R, V and Q, respectively, by titrimetry and 8.89±0.44, 10.41±0.54 and 10.41±0.52, in mg CO2 g−1 soil, for R, V and Q, respectively, for conductimetry. Excellent correlation (r=1.00) between titrimetry and conductimetry was observed. The decreasing order for respiration was E, H, L and T. After each incubation time, the conductimetric values were higher than those for titrimetry, for all treatments of these Brazilian soils. Average values of the exothermic thermal effect were: 0.58±0.02, 0.60±0.02 and 0.67±0.01 kJ g−1 soil, for R, V and Q, respectively, for 103 days. A significant correlation coefficient of 0.91 and P<0.0001 between calorimetric and respirometric values over 98 days was observed. Based on the obtained calorimetric results, it can be proposed that this technique should be as a useful analytical method for determining the microbial activity in soils. 相似文献
104.
105.
106.
This work was carried out when the last named author visited the Department of Mathematics of the University of Napoli Federico II in March 1994. He is very grateful for the hospitality he enjoyed and for the support by the C.N.R. 相似文献
107.
Silvana Franciosi Francesco de Giovanni 《Proceedings of the American Mathematical Society》1997,125(2):323-327
A subgroup of a group is said to be normal-by-finite if the core of in has finite index in . In this article groups satisfying the minimal condition on subgroups which are not normal-by-finite and groups with finitely many conjugacy classes of subgroups which are not normal-by-finite are characterized.
108.
Silvana Azzolini Travalon Inês Maria Costa Brighente Rosendo Augusto Yunes 《国际化学动力学杂志》2002,34(12):685-692
The plot of rate constants vs. pH for the dehydration step of the reaction between furfural and 5‐nitrofurfural with hydroxylamine, N‐methylhydroxylamine, and O‐methylhydroxylamine, shows two regions corresponding to the oxonium ion‐catalyzed and spontaneous dehydration. The oxonium ion‐catalyzed dehydration region of the reaction of furfural with the above mentioned hydroxylamines exhibits general acid catalysis with excellent Brønsted correlation (Brønsted coefficients: 0.76 (r = 0.986), 0.68 (r = 0.987), and 0.67 (r = 0.993) respectively). However, the rate constants of the spontaneous dehydration of these hydroxylamines, where water is considered the general acid catalyst, exhibit a large positive deviation from the Brønsted line. This fact was not observed in the reaction of non‐hydroxyl amines with different aromatic aldehydes by other authors, thus supporting that the spontaneous dehydration steps for these reactions proceed by intramolecular catalysis. The mechanism of intramolecular catalysis might be stepwise. First, a zwitterionic intermediate is formed. It can then evolve in the second step by loss of water, or follow a concerted pathway, with the transference of a proton through a five‐membered ring (general intramolecular acid catalysis). In the case of non‐hydroxyl amines, data suggested the possibility of a mechanism of intramolecular proton transfer through one or two water molecules, from the nitrogen of the amine to the leaving hydroxide ion. © 2002 Wiley Periodicals, Inc. Int J Chem Kinet 34: 685–692, 2002 相似文献
109.
Marianna Portaccio Daniela Durante Andrea Viggiano Silvana Di Martino Paola De Luca Daniela Di Tuoro Umberto Bencivenga Sergio Rossi Paolo Canciglia Bruno De Luca Damiano Gustavo Mita 《Electroanalysis》2007,19(17):1787-1793
Glucose microelectrodes were prepared by immobilizing glucose oxidase onto a cellulose acetate film coating a platinum wire. Hexamethylenediamine (HMDA) and Glutaraldehyde (GA) were employed as spacer and coupling agent, respectively. Sensitivities and linear response ranges were studied as a function of the relative amounts of HMDA and GA. The best sensitivity was found when HMDA and GA were 5% and 2.5% in aqueous solutions, respectively. Taking as a reference the functioning of this biosensor, the roles of HMDA and GA percentages appear to be opposed when the extension of the linear response range is considered. Indeed, an increase of one unit in HMDA percentage (from 5 to 6 %) induces an increase in the extension of the linear response range equal to that obtained with a decrease of one unit of GA percentage (from 2.5 to 1.5%). 相似文献
110.
Time-dependent density functional theory (TDDFT) and density functional-based molecular dynamics were used to simulate the finite temperature t(2g)5 e(g) <-- t(2g)6 absorption band of the Ru2+ hexahydrate coordination complex in aqueous solution. The (1)T1 <-- (1)A1 and (1)T2 <-- (1)A1 molecular term splitting of this transition, which is not accounted for by the Kohn-Sham excitation spectrum, is shown to be satisfactorily reproduced by TDDFT at the BLYP/ALDA level of theory. Comparison to the spectrum of the Ru2+ (H2O)6 complex in vacuo computed by similar density functional classical molecular dynamics methods leads to the observation that bulk solvation has a negligible effect on the position and the shape of the absorption profile. 相似文献