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91.
Nud'ga L. A. Petrova V. A. Ben'kovich A. D. Petropavlovskii G. A. 《Russian Journal of Applied Chemistry》2001,74(1):145-148
Sulfoethylation of the chitin-glucan complex, isolated from mycelium of the mold fungus Aspergillus niger, by substitution with sodium -chloroethylsulfonate or addition of sodium vinylsulfonate is examined. A comparative study is made of the reactivity of the chitin-glucan complex, chitosan, and cellulose in the both reactions. The sorption characteristics of the sulfoethylated products with respect to Cu(II) and Cr(III) are determined. 相似文献
92.
A. S. Shcheulin T. S. Semenova L. F. Koryakina M. A. Petrova A. K. Kupchikov A. I. Ryskin 《Optics and Spectroscopy》2007,103(4):660-664
The particular features of additive coloration—formation of color centers as a result of annealing in a reducing atmosphere—have been considered for two crystals with fluorite structure, calcium and cadmium fluorides. The significant differences in the processes of coloration of these crystals are related to both the chemical reactions on their surface and the interaction (or absence of such) between the two components diffusing into the crystal bulk: anion vacancies and electrons. 相似文献
93.
Solutions of bovine serum albumin with metal ions Pb2+ and Na+ were studied by fluorescence analysis in the visible and UV ranges in relation to such parameters of the medium as the concentration of macromolecules, the pH, and the ionic strength of the solution. The formation of nanoparticles, protein clusters, in aqueous solutions of albumin containing ions of such a heavy metal as lead was revealed by fluorescence polarization analysis. This investigation is of practical value for the solution of ecological and medical problems. 相似文献
94.
95.
Egor A. Kapitonov Natalia N. Petrova Vasilii V. Mukhin Leonid A. Nikiforov Vladimir D. Gogolev Ee Le Shim Aitalina A. Okhlopkova Jin-Ho Cho 《Molecules (Basel, Switzerland)》2021,26(4)
The physical and mechanical properties of nitrile–butadiene rubber (NBR) composites with N-cetylpyridinium bromide-carbon black (CPB-CB) were investigated. Addition of 5 parts per hundred rubber (phr) of CPB-CB into NBR improved the tensile strength by 124%, vulcanization rate by 41%, shore hardness by 15%, and decreased the volumetric wear by 7% compared to those of the base rubber-CB composite. 相似文献
96.
N. N. Tonkikh A. Strakovs K. V. Rizhanova M. V. Petrova 《Chemistry of Heterocyclic Compounds》2004,40(7):949-955
In reactions of 3-(5- and 5,6-substituted 2-aminophenylamino)-5,5-dimethylcyclohex-2-en-ones with carbaldehydes of pyridine, thiophene, and furan and substituted benzaldehydes, we have obtained 21 novel 7H-7-methoxycarbonyl-, 7-benzoyl-, 7-trifluoromethyl-, 7-nitro- and 7,8-dichloro-11-aryl-3,3-dimethyl-1,2,3,4,10,11-hexahydro-5H-dibenzo[b,e]-1,4-diazepin-1-one. 相似文献
97.
New method for obtaining highly dispersed manganese oxide under the action of a dc electric field was suggested. It was found that the electric field parameters affect the phase composition, shape, morphology and size of manganese oxide particles and the content of water. It is demonstrated that the manganese oxide synthesized can be used as a vulcanizing agent in manufacture of sealants based on thiocol and surpasses in application efficiency the analog produced by the conventional method. 相似文献
98.
Petrova T Okovytyy S Gorb L Leszczynski J 《The journal of physical chemistry. A》2008,112(23):5224-5235
Different possible pathways of the aminolysis reaction of succinic anhydride were investigated by applying high level electronic structure theory, examining the general base catalysis by amine and the general acid catalysis by acetic acid, and studying the effect of solvent. The density functional theory at the B3LYP/6-31G(d) and B3LYP/6-311++G(d,p) levels was employed to investigate the reaction pathways for the aminolysis reaction between succinic anhydride and methylamine. The single point ab initio calculations were based on the second-order M?ller-Plesset perturbation theory (MP2) with 6-31G(d) and 6-311++G(d,p) basis sets and CCSD(T)/6-31G(d) level calculations for geometries optimized at the B3LYP/6-311++G(d,p) level of theory. A detailed analysis of the atomic movements during the process of concerted aminolysis was further obtained by intrinsic reaction coordinate calculations. Solvent effects were assessed by the polarized continuum model method. The results show that the concerted mechanism of noncatalyzed aminolysis has distinctly lower activation energy compared with the addition/elimination stepwise mechanism. In the case of the process catalyzed by a second methylamine molecule, asynchronous proton transfer takes place, while the transition vectors of the acid-catalyzed transition states correspond to the simultaneous motion of protons. The most favorable pathway of the reaction was found through the bifunctional acid catalyzed stepwise mechanism that involves formation of eight-membered rings in the transition state structures. The difference between the activation barriers for the two mechanisms averages 2 kcal/mol at various levels of theory. 相似文献
99.
A. M. Gagarski I. S. Guseva V. E. Sokolov G. V. Val’ski G. A. Petrov D. O. Krinitsin D. V. Nikolaev T. A. Zavarukhina V. I. Petrova 《Bulletin of the Russian Academy of Sciences: Physics》2008,72(6):773-777
An experiment has been carried out to study neutron-neutron angular correlations in spontaneous fission of 252Cf. Angular dependences of the number of neutron-neutron coincidences obtained in the experiment were compared with the results of the Monte Carlo calculations for various neutron detection thresholds in the range 425–1600 keV. It was inferred that 10–11% of the total number of prompt neutrons from 252Cf (s.f.) in the laboratory system were emitted isotropically and may probably be interpreted as neutrons directly associated with the instant of scission of the nucleus. The analysis allowed their energy distribution to be determined as well. A similar method was also used to describe the angular correlation of prompt neutrons that accompanied the reaction 235U(n th ,f). 相似文献
100.
Anionic polymerization of methyl methacrylate in THF and toluene at ?70° was studied by means of i.r. spectroscopy. The reaction mixtures show characteristic absorption at 1600–1750 cm?1 caused by the stretching vibrations of the propagating centre as well as by the groups obtained in side reactions (metal splitting, addition to a carbonyl group, cyclization). Sec-butyllithium is more effective in THF than n-butyllithium, ethyllithium and fluorenyllithium. When polymerizing in toluene, small amounts of a donor (THF or HMPT) cause formation of active centres similar to those in pure THF. The “living” ends of oligo-MMA form 1:1 complexes with electron acceptors such as trialkylaluminium and triethylboron. 相似文献