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1.
We present a 3-12 GHz compact mixer-based reflectometer (CMR) and horn antenna system, and demonstrate its use in detecting backscatter signals with a free space calibration procedure. We evaluate the frequency-domain performance of the CMR-antenna system for measuring the complex reflection coefficient of a dielectric slab and compare it with that of a commercial vector network analyzer (VNA)-antenna setup. Time-domain responses are also investigated, and show the effectiveness of this calibration method. This low-cost, compact system eliminates the need for traditional mechanical standards and a VNA, is effective in reducing reflection artifacts, and allows for flexibility in the placement of reference planes; thus it is well suited for array-based imaging applications  相似文献   
2.
We report for the first time optical signal-to-noise penalties which lead to performance degradations in single-fiber long-reach optical access networks when compared to identical dual-fiber systems. A simplified architecture, with reduced optical amplifier count compared to previous work, for single-fiber operation of a symmetrical 10-Gb/s, 1024-way split, 110-km long-reach optical access network is presented and demonstrated. In addition, a possible solution to remove the optical signal-to-noise penalty is suggested  相似文献   
3.
Measurements of the dielectric breakdown strength of an arcing gap after current zero were made to determine the effects of arc chamber venting on the reverse recovery voltage needed to breakdown a recovering gap. The recovery conditions applied closely matched those created in a molded case circuit breaker under power line fault conditions. Three different vent sizes were used to determine the effect of gas pressure on the recovery characteristics of the plasma with recovery time between 170 /spl mu/s to 280 /spl mu/s, and currents from 3 kA/sub p/ to 15 kA/sub p/. Larger venting, providing increased cooling of the plasma, resulted in increased breakdown strength over the full range of currents. Based on the approximation that the recovering plasma breakdown strength is inversely proportional to plasma thermal temperature, breakdown voltage values were fitted to an exponential model to obtain plasma time constants and the initial holdoff voltage. Comparing these results to curve fits of E/p values showed E/p was a more accurate representation of the data. It is proposed to use E/p values when there is significant post current-zero chamber pressure. These results could be used as a guide to predicting molded case breaker interruption performance, especially for small arc chambers and short gaps.  相似文献   
4.
Due to the salient characteristics such as the time-varying and error-prone wireless links, the dynamic and limited bandwidth, the time-varying traffic pattern and user locations, and the energy constraints, it is a challenging task to efficiently support heterogeneous traffic with different quality of service (CoS) requirements in multihop mobile ad hoc networks. In the last few years, many channel-dependent mechanisms are proposed to address this issue based on the cross-layer design philosophy. However, a lot of problems remain before more efficient solutions are found. One of the problems is how to alleviate the conflict between throughput and fairness for different prioritized traffic, especially how to avoid the bandwidth starvation problem for low-priority traffic when the high-priority traffic load is very high. In this paper, we propose a novel scheme named Courtesy Piggybacking to address this problem. With the recognition of interlayer coupling, our Courtesy Piggybacking scheme exploits the channel dynamics and stochastic traffic features to alleviate the conflict. The basic idea is to let the high-priority traffic help the low-priority traffic by sharing unused residual bandwidth with courtesy. Another noteworthy feature of the proposed scheme is its implementation simplicity: The scheme is easy to implement and is applicable in networks using either reservation-based or contention-based MAC protocols.  相似文献   
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Pressurized hot water extraction (PHWE) using a laboratory made system was applied for the extraction of thermally labile and reasonably polar components such as berberine in coptidis rhizoma, glycyrrhizin in radix glycyrrhizae/liquorice and baicalein in scutellariae radix. PHWE was carried out dynamically at a flow of 1 ml/min, temperature between 95 and 140 °C, an applied pressure of 10-20 bar and extraction time of 40 min. Extraction by PHWE was found to give efficiencies comparable to Soxhlet extraction for baicalein in scutellariae radix and sonication for berberine in coptidis rhizoma, and glycyrrhizin in radix glycyrrhizae. Effects of ethanol added into the water used in PHWE were explored. Pressurized liquid extraction (PLE) with methanol as solvent was used for extraction of baicalein in scutellariae radix. The marker compounds present in the various medicinal plant extracts were determined by gradient elution HPLC.  相似文献   
8.
Enantioselective ester hydrolysis catalyzed by imprinted polymers   总被引:4,自引:0,他引:4  
Highly cross-linked network polymers prepared by molecular imprinting catalyzed enantioselectively the hydrolysis of N-tert-butoxycarbonyl phenylalanine-p-nitrophenyl ester (BOCPheONP). The templates were designed to allow incorporation of the key catalytic elements, found in the proteolytic enzyme chymotrypsin, into the polymer active sites. Three model systems were evaluated. These were constructed from a chiral phosphonate analogue of phenylalanine (series A, C) or L-phenylalanine (series B) attached by a labile ester linkage to an imidazole-containing vinyl monomer. Free radical copolymerization of the template with methacrylic acid (MAA) and ethylene glycol dimethacrylate (EDMA) gave a highly cross-linked network polymer. The templates could be liberated from the polymers by hydrolysis, giving catalytically active sites envisaged to contain an enantioselective binding site, a site complementary to a transition state like structure (series A, C), and a hydroxyl, imidazole, and carboxylic acid group at hydrogen bond distance. As predicted, the enantiomer of BOCPheONP complementary to the configuration of the template was preferentially hydrolyzed with D-selectivity for the series A polymers (kD/kL = 1.9) and L-selectivity for the series B polymers (kL/kD = 1.2). The maximum rate enhancement, when compared with a control polymer, prepared using a benzoyl-substituted imidazole monomer as template, was 2.5, and comparing with the imidazole monomer in solution, a maximum rate enhancement of 10 was observed. The catalytic activity was higher for polymers subjected to the nucleophilic treatment. This was explained by a higher site density and flexibility of the polymer matrix caused by this treatment. In a comparison of template rebinding to polymers imprinted with a template containing either a carboxylate (planar ground state structure) or a phosphonate (tetrahedral transition state like structure) functionality, it was observed that imprinted polymers are able to discriminate between a transition state like and a ground state structure for transesterification. However the influence of transition state stabilization on the observed rate enhancements remains obscure. Only at acidic pH's was catalysis observed, whereas at basic pH's the polymers inhibit the reaction. At a later stage, the catalytic activity of the polymers for nonactivated D- and L-phenylalanine ethyl esters was investigated. A rate enhancement of up to 3 was observed when compared to the blank. Most important, however, the polymers imprinted with a D template preferentially hydrolyzed the D-ethyl ester and exhibited saturation kinetics.  相似文献   
9.
An SCF perturbation method for investigating the effects of an arbitrary change in nuclear configuration on the electronic structure of a molecule is reported. Illustrative calculations for CO2 and CH3OH are presented. It is found that, when taken to second order, the error in the calculated change in energy which results from a change in nuclear configuration is typically in the range of 0.1 to 7%.  相似文献   
10.
A "ring expansion-annulation strategy" for the synthesis of substituted azulenes is described based on the reaction of beta'-bromo-alpha-diazo ketones with rhodium carboxylates. The key transformation involves an intramolecular Buchner reaction followed by beta-elimination of bromide, tautomerization, and in situ trapping of the resulting 1-hydroxyazulene as a carboxylate or triflate ester. Further synthetic elaboration of the azulenyl halide and sulfonate annulation products can be achieved by employing Heck, Negishi, Stille, and Suzuki coupling reactions. Reaction of the azulenyl triflate 84 with pinacolborane provides access to the azulenylboronate 91, which participates in Suzuki coupling reactions with alkenyl and aryl iodides. The application of these coupling reactions to the synthesis of biazulenes, terazulene 101, and related oligoazulenes is described, as well as the preparation of the azulenyl amino acid derivative 110.  相似文献   
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