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261.
This paper investigates the phenomenon of chaos synchronization of two different chaotic complex systems of the Chen and Lü type via the methods of active control and global synchronization. In this regard, it generalizes earlier work on the synchronization of two identical oscillators in cases where the drive and response systems are different, the parameter space is larger, and the dimensionality increases due to the complexification of the dependent variables. The idea of chaos synchronization is to use the output of the drive system to control the response system so that the output of the response system converges to the output of the drive system as time increases. Lyapunov functions are derived to prove that the differences in the dynamics of the two systems converge to zero exponentially fast, explicit expressions are given for the control functions and numerical simulations are presented to illustrate the success of our chaos synchronization techniques. We also point out that the global synchronization method is better suited for synchronizing identical chaotic oscillators, as it has serious limitations when applied to the case where the drive and response systems are different.  相似文献   
262.
Measurements of the electrical conductivity, Hall effect, thermnoelectric power were carried out in a wide temperature range (from about 170 to 475 K) for Ga2Se compound grown in single crystalline form. The present investigation revealed unusual observations in the Hall effect and the scattering mechanisms of the charge carriers indicating that Ga2Se is not a simple semiconductor. Also it showed that Ga2Se has a relatively high value of the thermoelectric power. A lot of physical parameters were deduced in the present study.  相似文献   
263.
The coupling of 1,2-bis(o-hydroxybenzamido)ethane 1 with two equivalents of the appropriate arenediazonium chloride in aqueous sodium hydroxide afforded the corresponding 1,2-bis(2-hydroxy-5-arylazobenzoylamino)ethanes 4–6 . The latter were converted to the corresponding dipotassium salts 7–9 , which were reacted with the appropriate dihalo compound or ditosylate in boiling DMF to give the corresponding 14-17-membered macrocyclic bis-azo-crowndilactams 10–18 in 58–65% yields. Compound 14 was N-alkylated to give the corresponding N,N′-dibenzyl derivative 19 .  相似文献   
264.
Electronic transport measurements were made on single crystal samples of Tl2Se3. The crystals were prepared by a special design based on Bridgman technique. The influence of temperature on the electrical conductivity, Hall effect, Hall mobility and the carrier concentration was investigated in the temperature range 200–400 K. The energy gap as well as the ionization energy were calculated. The scattering mechanism of the charge carrier was discussed in the same temperature range.  相似文献   
265.
Pexidartinib is the first drug approved by the U.S. Food and Drug Administration specifically to treat the rare joint tumor tenosynovial giant cell tumor. In the current study, a validated, selective, and sensitive UPLC-MS/MS assay was developed for the quantitative determination of pexidartinib in plasma samples using gifitinib as an internal standard (IS). Pexidartinib and IS were extracted by liquid-liquid extraction using methyl tert-butyl ether and separated on an acquity BEH C18 column kept at 40 °C using a mobile phase of 0.1% formic acid in acetonitrile: 0.1% formic acid in de-ionized water (70:30). The flow rate was 0.25 mL/min. Multiple reaction monitoring (MRM) was operated in electrospray (ESI)-positive mode at the ion transition of 418.06 > 165.0 for the analyte and 447.09 > 128.0 for the IS. FDA guidance for bioanalytical method validation was followed in method validation. The linearity of the established UPLC-MS/MS assay ranged from 0.5 to 1000 ng/mL with r > 0.999 with a limit of quantitation of 0.5 ng/mL. Moreover, the metabolic stability of pexidartinib in liver microsomes was estimated.  相似文献   
266.
6‐Amino‐2‐thioxotetrahydropyrimidine‐5‐carbonitrile derivative 2 was synthesized in a good yield via refluxing a mixture of arylidene 1 and thiourea in a highly basic sodium ethoxide solution. Subsequently, the synthesized pyrimidine‐2‐thione derivative 2 was allowed to interact with diversified nucleophiles and electrophiles under various reaction conditions in order to have a feasible access to further new and assorted fused heterocycles. Finally, the biological activity of the newly synthesized fused pyrimidines was screened in vitro against four different Gram‐positive and Gram‐negative bacterial strains. All the developed heterocycles were adequately characterized utilizing 1H‐NMR, 13C‐NMR, Fourier transform infrared, elemental analysis, and electrospray ionization–mass spectrum and tested for their antibacterial activity.  相似文献   
267.
Processing technique and storage conditions are the main factors that affect the phytochemical profile of Not-from-Concentrate (NFC) juice, which could decrease the nutritional and bioactive properties of the corresponding juice. The aim of this study was to evaluate the quality changes that occurred in NFC mango juice after Ohmicsonication (OS) and during storage in comparison to other processing methods such as sonication (S), thermosonication (TS), ohmic heating (OH), and conventional heating (CH). Quality attributes such as polyphenoloxidase (PPO) and pectinmethylesterase (PME) activities, ascorbic acid and hydroxymethyl furfural (HMF) contents, total phenolics, total flavonoids, total carotenoids, electric conductivity, color values and microbial load (total plate count, mold, yeast, and psychrophilic bacteria) were examined. OS and OH treatments demonstrated the highest inactivation of PPO (100%), while CH and TS displaying inhibitions 89% and 90%, respectively and only S treatment exhibited insufficient inactivation of both PPO and microbial load. However, the inhibition of PME followed the order OS (96.5%) > OH (94.9%) > TS (92.5%) > CH (88.5%). The best treatment, with the highest retention of phytochemical contents (ascorbic acid, total carotenoids, antioxidant activity, total flavonoids, and total phenolic content) for NFC mango juice and during storage was obtained with OS treated samples compared to other treatments (in the order from the lowest to highest percentage, OS < OH < TS < CH). Consequently, the results indicated that OS could be applied as a new mild thermal treatment in the production of mango juice with improved quality properties of stored NFC mango juice.  相似文献   
268.
Single crystals of GaTe were prepared in our laboratory by a special modified Bridgman technique method. Measurements of the electrical conductivity and Hall effect between 210 and 450 K were carried out on GaTe samples in two crystallographic directions. The Hall coefficient is positive and varies with the crystallographic direction. A unique mobility behaviour and strong anistropy in the carrier mobility were observed. The Hall mobilities parallel and perpendicular to the C-axis, at room temperature, were 12 cm/V · s and 25.12 cm2/V ·s, respectively. The free carrier concentration lies between 1013 − 1014 cm−3 at room temperature.  相似文献   
269.
Piperazine-based dithiocarbamates serve as important scaffolds for numerous pharmacologically active drugs. The current study investigates the design and synthesis of a series of dithiocarbamates with a piperazine unit as well as their biological activities. Under ultrasound conditions, the corresponding piperazine-1-carbodithioates 5a–5j were synthesized from monosubstituted piperazine 2 and N-phenylacetamides 4a–4j in the presence of sodium acetate and carbon disulfide in methanol. The structures of the newly synthesized piperazines were confirmed, and their anti-lung carcinoma effects were evaluated. A cytotoxic assay was performed to assess the hemolytic and thrombolytic potential of the synthesized piperazines 5a–5j. The types of substituents on the aryl ring were found to affect the anticancer activity of piperazines 5a–5j. Piperazines containing 2-chlorophenyl (5b; cell viability = 25.11 ± 2.49) and 2,4-dimethylphenyl (5i; cell viability = 25.31 ± 3.62) moieties demonstrated the most potent antiproliferative activity. On the other hand, piperazines containing 3,4-dichlorophenyl (5d; 0.1%) and 3,4-dimethylphenyl (5j; 0.1%) rings demonstrated the least cytotoxicity. The piperazine with the 2,5-dimethoxyphenyl moiety (5h; 60.2%) showed the best thrombolytic effect. To determine the mode of binding, in silico modeling of the most potent piperazine (i.e., 5b) was performed, and the results were in accordance with those of antiproliferation. It exhibits a similar binding affinity to PQ10 and an efficient conformational alignment with the lipophilic site of PDE10A conserved for PQ10A.  相似文献   
270.
Molecular Diversity - A new series of 6-substituted quinolin-2-one thiosemicarbazides 6a–j has been synthesized. The structure of the target compounds was proved by different spectroscopic...  相似文献   
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