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101.
In solving multi-objective optimization problems, evolutionary algorithms have been adequately applied to demonstrate that multiple and well-spread Pareto-optimal solutions can be found in a single simulation run. In this paper, we discuss and put together various different classical generating methods which are either quite well-known or are in oblivion due to publication in less accessible journals and some of which were even suggested before the inception of evolutionary methodologies. These generating methods specialize either in finding multiple Pareto-optimal solutions in a single simulation run or specialize in maintaining a good diversity by systematically solving a number of scalarizing problems. Most classical generating methodologies are classified into four groups mainly based on their working principles and one representative method from each group is chosen in the present study for a detailed discussion and for its performance comparison with a state-of-the-art evolutionary method. On visual comparisons of the efficient frontiers obtained for a number of two and three-objective test problems, the results bring out interesting insights about the strengths and weaknesses of these approaches. The results should motivate researchers to design hybrid multi-objective optimization algorithms which may be better than each of the individual methods. 相似文献
102.
103.
Ions undergoing a reaction-diffusion process are susceptible to electric field. We show that a constant external field may induce a kind of instability on the state stabilized by diffusion in a reaction-diffusion system giving rise to formation of pattern even when the diffusion coefficients of the reactants are equal. The origin of the pattern is due to the difference in mobilities of the two species and is thus markedly different from that of deformed Turing pattern in presence of the field. While this differential flow instability had been shown earlier to result in traveling waves, we realize in the context of stationary pattern formation in a typical reaction-diffusion-advective system. Our analysis is based on a numerical simulation of a generic model on a two-dimensional domain. 相似文献
104.
Pramil C. Deb 《European Polymer Journal》1982,18(9):769-771
An extended mathematical analysis is proposed for free-radical polymerisation systems involving initiators which produce primary radicals that have quite long half-life and decompose to secondary radicals. Initiation and macroradical termination by both primary and secondary radicals have been considered. Data for styrene and vinyl chloride have been treated with the developed relationships; limitations of earlier treatments are discussed. 相似文献
105.
Sambasivarao Kotha Kalyaneswar Mandal Ashoke Chandra Deb Shaibal Banerjee 《Tetrahedron letters》2004,45(52):9603-9605
A fast, efficient and environmentally benign solvent-free procedure has been developed for microwave-assisted Claisen rearrangement on a silica gel support. Various bis-allyl ketones were prepared using this protocol. 相似文献
106.
107.
Acrylic acid was grafted onto fluorinated ethylene propylene copolymer (FEP) using a simultaneous radiation technique and the resulting membranes were subsequently sulfonated. Thermal and mechanical properties of these membranes were investigated and were found to be strongly influenced by the degree of grafting. Thermogravimetric analysis (TGA) of these membranes showed that these membranes undergo multistep degradation unlike virgin FEP which degrades in a single step. Glass transition temperature and degree of crystallinity were determined by differential scanning calorimetry (DSC). Glass transition temperature increased while crystallinity decreased with increase in degree of grafting. Tensile strength and elongation at break were found to decrease on grafting and further on sulfonation. Copyright © 2004 John Wiley & Sons, Ltd. 相似文献
108.
Biswas S Hussain SA Deb S Nath RK Bhattacharjee D 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2006,65(3-4):628-632
This communication reports the formation of complex Langmuir monolayer at the air-water interface with the water-soluble N-cetyl N,N,N-trimethyl ammonium bromide (CTAB) molecules when interacted with the stearic acid (SA) molecules. The reaction kinetics of the formation of the CTAB-SA complex was monitored by observing the surface pressure versus time graph. Multilayered LB films of this complex doped with Congo red was successfully formed onto a quartz substrate. UV-Vis absorption and steady-state fluorescence spectroscopic characteristics of this doped LB films confirms the successful incorporation of Congo red molecules in to the CTAB-SA complex films. 相似文献
109.
Rajdip Roy Dr. Jolly Deb Dr. Siddhartha Sankar Jana Prof. Parthasarathi Dastidar 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(47):15320-15324
A simple strategy for designing salt‐based supramolecular gelators comprised of various nonsteroidal anti‐inflammatory drugs (NSAIDs) and amantadine (AMN) (an antiviral drug) has been demonstrated using a supramolecular synthon approach. Single‐crystal and powder X‐ray diffraction established the existence of the well‐studied gel‐forming 1D supramolecular synthon, namely, primary ammonium monocarboxylate (PAM) synthon in all the salts. Remarkably five out of six salts were found to be capable of gelling methyl salicylate (MS)—an important ingredient in commercially available topical gels; one such selected biocompatible salt displayed an anti‐inflammatory response in prostaglandin E2 (PGE2) assay, thereby indicating their plausible biomedical applications. 相似文献
110.
Dr. Virginia M. Cangelosi Dr. Aniruddha Deb Prof. James E. Penner‐Hahn Prof. Vincent L. Pecoraro 《Angewandte Chemie (International ed. in English)》2014,53(30):7900-7903
Protein design will ultimately allow for the creation of artificial enzymes with novel functions and unprecedented stability. To test our current mastery of nature’s approach to catalysis, a ZnII metalloenzyme was prepared using de novo design. α3DH3 folds into a stable single‐stranded three‐helix bundle and binds ZnII with high affinity using His3O coordination. The resulting metalloenzyme catalyzes the hydration of CO2 better than any small molecule model of carbonic anhydrase and with an efficiency within 1400‐fold of the fastest carbonic anhydrase isoform, CAII, and 11‐fold of CAIII. 相似文献