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81.
Achieving good quality of products from plastic injection moulding processes is very challenging, since the process comprises many affecting parameters. Common defects such as warpage are hard to avoid, and the defective parts will eventually go to waste, leading to unnecessary costs to the manufacturer. The use of recycled material from postindustrial waste has been studied by a few researchers. However, the application of an optimisation method by which to optimise processing parameters to mould parts using recycled materials remains lacking. In this study, Response Surface Methodology (RSM) and Particle Swarm Optimisation (PSO) methods were conducted on thick plate parts moulded using virgin and recycled low-density polyethylene (LDPE) materials (100:0, 70:30, 60:40 and 50:50; virgin to recycle material ratios) to find the optimal input parameters for each of the material ratios. Shrinkage in the x and y directions increased in correlation with the recycled ratio, compared to virgin material. Meanwhile, the tensile strength of the thick plate part continued to decrease when the recycled ratio increased. R30 (70:30) had the optimum shrinkage in the x direction with respect to R0 (100:0) material where the shrinkage increased by 24.49% (RSM) and 33.20% (PSO). On the other hand, the shrinkage in the y direction for R30 material increased by 4.48% (RSM) and decreased by 2.67% (PSO), while the tensile strength of R30 (70:30) material decreased by 0.51% (RSM) and 2.68% (PSO) as compared to R0 (100:0) material. Validation tests indicated that the optimal setting of processing parameter suggested by PSO and RSM for R0 (100:0), R30 (70:30), R40 (60:40) and R50 (50:50) was less than 10%.  相似文献   
82.
During the steel production process, nearly twice as many input materials are used as compared to finished products. This creates a large amount of post-production waste, including slag, dust, and sludge. New iron production technologies enable the reuse and recycling of metallurgical waste. This paper presents an investigation on the reduction of selected iron-bearing waste materials in a laboratory rotary furnace. Iron-bearing waste materials in the form of dust, scale, and sludge were obtained from several Polish metallurgical plants as research material. A chemical analysis made it possible to select samples with sufficiently high iron content for testing. The assumed iron content limit in waste materials was 40 wt.% Fe. A sieve analysis of the samples used in the subsequent stages of the research was also performed. The tests carried out with the use of a CO as a reducer, at a temperature of 1000 °C, allowed to obtain high levels of metallization of the samples for scale 91.6%, dust 66.9%, and sludge 97.3%. These results indicate that in the case of sludge and scale, the degree of metallization meets the requirements for charge materials used in both blast furnace (BF) and electric arc furnace (EAF) steelmaking processes, while in the case of reduced dust, this material can be used as enriched charge in the blast furnace process. Reduction studies were also carried out using a gas mixture of CO and H2 (50 vol.% CO + 50 vol.% H2). The introduction of hydrogen as a reducing agent in reduction processes meets the urgent need of reducing CO2 emissions. The obtained results confirm the great importance and influence of the selection of the right amount of reducer on the achievement of a high degree of metallization and that these materials can be a valuable source of metallic charge for blast furnace and steelmaking processes. At an earlier stage of the established research program, experiments of the iron oxides reduction from iron-bearing waste materials in a stationary layer in a Tammann furnace were also conducted.  相似文献   
83.
Textile materials produced from a high tenacity industrial polyester fiber are most widely used in the mechanical rubber goods industry to reinforce conveyor belts, tire cords, and hoses. Reinforcement of textile rubber undergoes a vulcanization process to adhere the textile materials with the rubber and to enhance the physio-mechanical properties of the product. The vulcanization process has an influence on the textile material being used as a reinforcement. In this work, the effects of aging temperature and time on the high tenacity polyester yarn’s mechanical and surface structural properties were investigated. An experiment was carried out on a pre-activated high tenacity polyester yarn of different linear densities, by aging the yarn specimens under various aging temperatures of 140, 160, 200, and 220 °C for six, twelve, and thirty-five minutes of aging time. The tensile properties and surface structural change in the yarns pre- and post-aging were studied. The investigation illustrates that aging time and temperature influence the surface structure of the fiber, tenacity, and elongation properties of the yarn. Compared to unaged yarn, an almost five times higher percentage of elongation was obtained for the samples aged at 220 °C for 6 min, while the lowest tenacity was obtained for the sample subjected to aging under 220 °C for 35 min.  相似文献   
84.
Al-Zn-In alloys having 4.2% zinc content and various indium content in the range of 0.02–0.2% were tested with respect to the most important electrochemical properties of sacrificial anodes in a cathodic protection, i.e., the current capacity and potential of the operating anode. The distribution of In and Zn in the tested alloys was mapped by means of the EDX technique, which demonstrated that these elements dissolve well in the alloy matrix and are evenly distributed within it. The current capacity of such alloys was determined by means of the method of determining the mass loss during the dissolution by a current of known charge. The results obtained demonstrate that the current capacity of Al-Zn-In alloy decreases with the increase in the In content, which results in an increased consumption of anode material and shorter lifetime of anodes. With 0.02% In content, the capacity amounted to approx. 2500 Ah/kg, whereas the alloy with 0.2% In had as much as 30% lower capacity amounting to approx. 1750 Ah/kg. Microscopic examination for the morphology and surface profile of the samples after their exposure demonstrated that a higher indium content in the alloy results in a more uneven general corrosion pattern during the dissolution of such alloy, and the cavities (pits) appearing on the alloy surface are larger and deeper. As the indium content is increased from 0.02% to 0.05%, the Al-Zn-In alloy potential decreases by about 50 mV to −1100 mV vs. Ag/AgCl electrode, which is advantageous in terms of using this alloy as a sacrificial anode. When the indium content is further increased from 0.05% to 0.2%, the potential of the alloy is no longer changed to a more negative one. The results obtained from all these tests demonstrate that alloys containing up to 0.05% of In additive are practically applicable for cathodic protection.  相似文献   
85.
The study analyzed potential applicability for asymmetric reinforcement of glulam beams using materials with a higher modulus of elasticity. Reinforcement elements included smooth and ribbed steel rods as well as basalt rods. These rods were placed only in the tensile zone, assuming that they will not only impart increased rigidity but first of all will reduce the scatter of bending strength values. What is significant, tests were conducted on timber with defects, as it is most commonly used in industrial practice. Analyses showed that this provides an increase in rigidity close to the assumed level. A significant increase in strength was observed. The manufactured beams reinforced with steel and basalt rods were characterized by mean bending strength amounting to 54 and 47 N/mm2, respectively. However, no significant improvement was found in the scatter of the observed variable. Beams reinforced with steel exhibit a 20% higher strength than unreinforced beams. The lower strength of beams reinforced with basalt bars may be related to the lower modulus of elasticity of the basalt itself.  相似文献   
86.
Foundation piles that are made by concrete 3D printers constitute a new alternative way of founding buildings constructed using incremental technology. We are currently observing very rapid development of incremental technology for the construction industry. The systems that are used for 3D printing with the application of construction materials make it possible to form permanent formwork for strip foundations, construct load-bearing walls and partition walls, and prefabricate elements, such as stairs, lintels, and ceilings. 3D printing systems do not offer soil reinforcement by making piles. The paper presents the possibility of making concrete foundation piles in laboratory conditions using a concrete 3D printer. The paper shows the tools and procedure for pile pumping. An experiment for measuring pile bearing capacity is described and an example of a pile deployment model under a foundation is described. The results of the tests and analytical calculations have shown that the displacement piles demonstrate less settlement when compared to the analysed shallow foundation. The authors indicate that it is possible to replace the shallow foundation with a series of piles combined with a printed wall without locally widening it. This type of foundation can be used for the foundation of low-rise buildings, such as detached houses. Estimated calculations have shown that the possibility of making foundation piles by a 3D printer will reduce the cost of making foundations by shortening the time of execution of works and reducing the consumption of construction materials.  相似文献   
87.
The objective of the reported project was to produce wood agglomerates from popular East European species to determine their strength and combustion properties. Closed-die pellets were produced from sawdust of six types of wood common on the East European market: pine, willow, oak, poplar, birch, and beech. The properties of pellets, determined by the type of wood, were influenced by the compaction pressure and the moisture content of the sawdust. The highest average pellet density was obtained for oak sawdust, while the lowest density was obtained for poplar pellets. Expansion of pellets after removing from the die was found to be dependent on the wood species, and as expected, on compaction pressure. The pellet expansion increased after 2 h of conditioning in the laboratory and with an increase in moisture content. The highest and the smallest strength were obtained for oak pellets and for birch sawdust, respectively. The strength of the pellets increased by more than 100% with an increase in the compaction pressure from 60 MPa to 120 MPa. The average strength decreased by 65% with increasing moisture content. For all tested materials, drop resistance remained at a high level, acceptable in industrial practice. The highest calorific value of 18.97 MJ/kg was obtained for pine pellets. The highest ash value of 1.52% was obtained for willow pellets and the lowest value of 0.32% for pine pellets.  相似文献   
88.
A new approach to the synthesis of asymmetrical cyclic compounds using a stilbene scaffold has been developed. The use of boron trifluoride diethyl etherate as the catalyst, both with and without paraformaldehyde, allows us to obtain new substituted dioxanes, oxanes, cyclic compounds or dimer. The analysis of products was run using experimental and theoretical methods.

A new approach to the synthesis of asymmetrical cyclic compounds using a stilbene scaffold has been developed.

Various macrocycles have been widely investigated due to their interesting conformational characteristics and abundant host–guest properties. New macrocyclic receptors with high selectivity in molecular recognition are being looked for,1 because they have many possible applications in the construction of diverse supramolecular systems.2–15 In particular, various drug-delivery systems for tumours are being tested and looked at. Development of most solid tumours is strictly associated with the formation of their own functional vascular supply, the network of which is typically obtained in the process of angiogenesis from the host''s normal vascular system. The particular occurrence of tumour neo-vasculature is regarded as a well-fitting target for cancer cell annihilation. Two forms of vascular targeting agents (VTAs) can be distinguished. The first category concerns the substances that inhibit the angiogenesis process (they are referred to as the angiogenesis inhibitors, AIs). The second variant (referred to as the vascular disrupting agents, VDAs),16 are the compounds harmful to the already-established vessels. Combretastatins CA1P (OXi4503) and CA4P (a subtype of natural phenols) are new vascular disrupting and vascular targeting agents.16 They exhibit significant abilities of gastric tumour metastasis inhibition and of antitumor immune reactivity enhancement.17 These compounds additionally contain a notable characteristic of differentiated methoxy groups in the framework. Continuing our study concerning the synthesis and searching the biological activity of stilbenes18 and drug-delivery systems for tumours, we directed our attention to the new substituted dioxanes, oxanes, and cyclic compounds. We conducted studies on the reaction of substituted stilbenes and paraformaldehyde in the presence of a Lewis acid as the catalyst (BF3·OEt2) (and2).2). The acid-catalyzed condensation of olefins with aldehydes, the Prins reaction, is generally used for the preparation of 1,3-dioxanes.19 The major products of the classical Prins reaction are normally 1,3-dioxanes, 1,3-glycols, or unsaturated alcohols depending on the reaction conditions19 (Fig. 1). The aza-Prins cyclization, which is the nitrogen version of the reaction, is of particular interest. The reaction permits rapid access to azaheterocycles and the wide applicability and usefulness of the aza-Prins reaction have been demonstrated by the synthesis of a variety of complex natural products.20The compounds of (7–10) obtained from the reaction of suitable stilbene derivatives (1–4) with paraformaldehyde and BF3·OEt2 as the catalysta
EntryR1R2R3R4R5Yield (%)
1/7HBrHHH25
2/8HBrHHNO220
3/9OCH3HOCH3NO2NO2A little
4/10HOCH3HHBr25
Open in a separate windowaTr-room temperature, stoichiometry of substates 1 mmol : 1 mmol, BF3·OEt2-2 mmol, time reaction-3 h (above 3 h increased the yield of the polymeric product).The compound of (11) obtained from reaction of (4) with BF3·OEt2 as the catalyst and paraformaldehyde. Products (12 and 13) were achieved also without paraformaldehyde
EntryR1R2R3R4R5R6Yield (%)
4/11HOCH3HHBrH60
5/12HOCH3HHOCH3H70
6/13OCH3OCH3OCH3HBrH80
Open in a separate windowOpen in a separate windowFig. 1Prins reaction.It is known that catalyst influence stereocontrol of Prins cyclization. For example, in Prins cyclization various aldehydes and dienyl alcohols catalyzed by a confined chiral imidodiphosphoric acid (IDP), the 2,3-disubstituted tetrahydrofurans, are obtained products with excellent diastereo- and enantioselectivities.20e In the case of rhenium(vii) complex, an effective catalyst for Prins cyclizations using aromatic and α and β-unsaturated aldehydes, the substituted 4-hydroxytetrahydropyran products are formed stereoselectively.20d Therefore, we assumed that the reaction with the stilbenes would also be stereoselective. The reaction of bromostilbene (1), 4-bromo-4′-nitrostilbene (2) and 3,5-dimethoxy-2′,4′-dinitrostilbene (3) with paraformaldehyde occurs according to the Prins mechanism and are obtained 1,3-dioxanes (7–9) (). 13C NMR resonances were assigned unequivocally, based on the combined information from 1D to 2D NMR (gCOSY, gHSQC and gHMBC) experiments. Coupling constants (1H–1H) were measured directly from resolution-enhanced 1D spectra and confirmed, when necessary, by homo-decoupling. gHSQC and gHMBC analysis allowed the assignment of the compounds regiochemistry. The stereochemistry of the obtained products was determined by coupling constants from 1H NMR spectra (see ESI). All coupling constants in (7, 8, 10) for protons H4–H5, H5–H6 are about 10 Hz (axial–axial position, a–a), because the benzene rings are predominantly in the equatorial position. In the case of the product (11), the coupling constants for protons H2–H3 and H3–H4 are about 10 Hz (protons in a–a position and benzene rings in equatorial position) but the coupling constants for protons H4–H5 are about 4 Hz. This shows that the remaining H5 proton is predominantly in the equatorial position in relation to the H4. For compounds (12, 13) the coupling constants for protons H1–H2, H2–H3 and H3–H4 are about 10–11 Hz (the coupling for H3–H4′ is about 4 Hz). This shows that all the rings are predominantly in equatorial position in relation to the previous one. The stereochemistry of products depends on the reaction mechanism. In all instances, substrates (1–4) were converted to 1,3-dioxanes (7–10) in the Prins reactions (Fig. 2). Accordingly, the stilbene is attacked by an activated formaldehyde species (complex H2CO·BF3·OEt2) in the first step of the reaction. Since a cyclization to a four-membered oxetane is disfavoured, the second formaldehyde molecule is connected, leading to 1,3-dioxane. The cyclization precursor (for substrates 1–4) is presumably the chiral carbenium ion I. The two faces of the carbenium ion are diastereotopic due to the communicating stereogenic center. A differentiation results from the difference in size of the hydrogen atom and the phenyl moiety. The hydrogen atom assumes the pseudoaxial position in the transition state of cyclization, as is presented in Fig. 2. The supposition of the carbenium ion intermediate is consistent with the observed stereoconvergency of the reaction for the 1-phenylpropen-1-en.20 Another main product was obtained with 4-bromo-4′-methoxystilbene (11) in addition to Prins (10).Open in a separate windowFig. 2Putative intermediate I en route to the formation compounds 1,3-dioxanes (7–10).The compound (11) is built with two scaffolds of 4-bromo-4′-methoxystilbene and one molecule of formaldehyde. It can be observed that the regiochemistry and stereochemistry for the one molecule of stilbene are the same for (11) and (10). It is worth noting that due to the steric bulk of Lewis acid (2,6-di-tert-butylphenoxy)difluoroborane, a potential electrophilic complex H2CO·BF2·OAr (Bach and Löbel21) is sensitive towards the substitution patterns in β-substituted styrenes. Whereas 1-phenylprop-1-ene showed reactivity, other bulk styrenes did not react at all. The catalyst BF3·OEt2 is not so steric-limited and probably in Prins reaction product (10) is obtained. The stereochemistry of the obtained products was determined by coupling constants from 1H NMR spectra. The course of reaction toward product (10) relates to the mesomeric effect of the methoxy group, which stabilizes the positive charge on carbon atom α compared to the rest of the molecule. The mechanism of reaction for product (11) is unknown. Presumably, the product is obtained from carbenium ion II (Fig. 3). It is formed from one molecule of formaldehyde, one molecule of stilbene derivative and BF3·OEt2. This intermediate reacts with the next polarizable molecule of substituted stilbene. The hypothesis of II carbenium ion intermediate is compliant with the regiochemical course of reaction toward product (11). As it was already mentioned, the stereochemistry for the first molecule of stilbene is the same for (11) and (10) (protons H2–H3 and H3–H4 are in the axial–axial position, and the H5 proton is in the equatorial position). Probably, the arrangement of the second stilbene molecule depends on hindrances in the forming product. In turn, asymmetrical cyclic products (12, 13) are created from symmetrical (5) and asymmetrical (6) substrates.Open in a separate windowFig. 3Putative intermediate II en route to the formation compound (11).In this case, two stilbene molecules react with each other in the presence of Lewis acid as a catalyst and with paraformaldehyde (Fig. 4).Open in a separate windowFig. 4Suggested mechanism of creation of the cyclic stilbenes (12) and (13).When the reactions were carried out without paraformaldehyde products (12) and (13) were obtained. We concluded that the addition of these compounds did not affect the course of the reaction. Moreover, the product is not observed when there is no catalyst in the reaction. The substrates (5) or (6) react with the aromatic ring of the second stilbene in Diels–Alder cyclization (the diene moiety is activated by methoxy group, and the dienophile is catalyzed by the Lewis BF3·OEt2 acid). After the Diels–Alder reaction, the proton movement leads to the tetralin (12) and (13). Note that the presented syntheses allow the preparation of a wide range of polycyclic aromatic arenes as well as heteroarene structures. After optimization of the reaction conditions in the presence of BF3·OEt2 with respect to the reaction solvent, temperature, and catalyst amount, the cyclic compounds (12) and (13) were prepared in 90% and 85% yields, respectively. According to the method presented in ref. 22, where iodine was found to be an effective reagent for cross-coupling of olefins with aldehydes to produce 1,3-dioxane derivative, we examined this reaction with paraformaldehyde and (1–6). It is notable that only for substrate (5) the reaction proceeded and product (12) was obtained. Product (12), similarly to the reaction with BF3·OEt2, was created independently of the paraformaldehyde presence (yield 70% with paraformaldehyde or 90% without it). We concluded that BF3·OEt2 was a more effective reagent than iodine in the presented reactions. Because of the chemical activity of the olefin bond of 1,2-diphenylethylene, stilbene is not a suitable starting compound for synthesis of stilbene derivatives, which is why we explored dibenzo[b,f]oxepin (14a). Moreover, this structure is an important scaffold in medicinal chemistry and molecules with this skeleton exhibit medicinal and drug properties.16–18 With this aim in mind, we used in the synthesis methoxy dibenzo[b,f]oxepin and obtained dimer (15) (100% yield), in which the olefin bond was not reacting and the scaffold of Z-stilbene was preserved (Fig. 5). In order to expand the scope of this reaction, we examined the reaction of (14a) with (14b) (Fig. 5).Open in a separate windowFig. 5The formation of dimer (15) and product (16).This process was successfully conducted, which enables the incorporation of aryl groups (product 16, 60% yield) to the dibenzo[b,f]oxepin framework. Considering that the combination of experimental and computational work should allow a complete characterization of the compounds and in order to explain the selectivity of cyclization, we calculated energy minima of the reactants in solution and NMR parameters (see ESI). The optimum structure of 12, 13, 15, 16 using the DFT B3LYP/6-31G* method was calculated. The influence of the solvent was described using the polarizable continuum model (PCM). Proton and 13C carbon chemical shifts were calculated using GIAO-DFT method. The conclusions coming from comparison of the experimental and theoretical spectra have supported the adopted signal assignments and confirmed the structure.In summary, we have developed a new easy synthesis of asymmetrical cyclic compounds derivatives of tetralin with high yield. What is notable, when the asymmetrically substituted (also with different groups) stilbenes reacted, dioxanes and oxanes were created respectively. Our study has provided a very concise method of constructing the derivative dibenzo[b,f]oxepin framework. Such structures can be easily transformed into branched stilbene molecules. Furthermore, products (12), (13), (15) and (16) are interesting building blocks for synthesis and the biological activity of the obtained molecules will be investigated and tested for/as nanoplatforms system drug-delivery systems for tumours.23  相似文献   
89.
90.
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