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931.
932.
Kyungnam Kim Dongsuk Yoo Hyekyoung Choi Dr. Sudarsan Tamang Jae‐Hyeon Ko Sungwoo Kim Prof. Yong‐Hyun Kim Prof. Sohee Jeong 《Angewandte Chemie (International ed. in English)》2016,55(11):3714-3718
Wet chemical synthesis of covalent III‐V colloidal quantum dots (CQDs) has been challenging because of uncontrolled surfaces and a poor understanding of surface–ligand interactions. We report a simple acid‐free approach to synthesize highly crystalline indium phosphide CQDs in the unique tetrahedral shape by using tris(dimethylamino) phosphine and indium trichloride as the phosphorus and indium precursors, dissolved in oleylamine. Our chemical analyses indicate that both the oleylamine and chloride ligands participate in the stabilization of tetrahedral‐shaped InP CQDs covered with cation‐rich (111) facets. Based on density functional theory calculations, we propose that fractional dangling electrons of the In‐rich (111) surface could be completely passivated by three halide and one primary amine ligands per the (2×2) surface unit, satisfying the 8‐electron rule. This halide–amine co‐passivation strategy will benefit the synthesis of stable III‐V CQDs with controlled surfaces. 相似文献
933.
In this paper we study the spectral properties of (m, C)-isometric operators. In particular, if \(T\in \mathcal{{L(H)}}\) is (m, C)-isometric operators, then the power of (m, C)-isometric operators is also (m, C)-isometric operators. Moreover, if \(T^{*}\) has the single-valued extension property, then T has the single-valued extension property. Finally, we investigate conditions for (m, C)-isometric operators to be (1, C)-isometric operators. 相似文献
934.
Field-amplified sample stacking (FASS) in capillary electrophoresis (CE) was used to determine the concentration of donepezil, an acetylcholinesterase inhibitor, in human plasma. A sample pretreatment by liquid-liquid extraction with isopropanol/n-hexane (v/v 3:97) and subsequent quantification by FASS-CE was used. Before sample loading, a water plug (0.5 psi, 6 s) was injected to permit FASS. Electrokinetic injection (7 kV, 90 s) was used to introduce sample cations. The separation condition for donepezil was performed in electrolyte solutions containing Tris buffer (60 mM, pH 4.0) with sodium octanesulfonate 40 mM and 0.01% polyvinyl alcohol as a dynamic coating to reduce analytes' interaction with capillary wall. The separation was performed at 28 kV and detected at 200 nm. Using atenolol as an internal standard, the linear ranges of the method for the determination of donepezil in human plasma were over a range of 1-50 ng/mL. The limit of detection was 0.1 ng/mL (S/N=3, sampling 90 s at 7 kV). One female volunteer (54 years old) was orally administered a single dose of 10 mg donepezil (Aricept, Eisai), and blood samples were drawn over a 60 h period for pharmacokinetic study. The method was also applied successfully to monitor donepezil in sixteen Alzheimer's disease patients' plasmas. 相似文献
935.
A cation-selective exhaustive injection and sweeping micellar EKC (CSEI-Sweep-MEKC) was established to analyze morphine and its four metabolites, including codeine, normorphine (NM), morphine-3-glucuronide (M3G), and morphine-6-glucuronide (M6G). After SPE, the urine samples were analyzed by this CE method. The phosphate buffer (75 mM, pH 2.5) containing 30% methanol was first filled into an uncoated fused-silica capillary (40 cm, 50 microm id), then a high-conductivity buffer (120 mM phosphate, 10.3 kPa for 99.9 s) followed. The pretreated urine sample was loaded by electrokinetic injection (10 kV, 600 s). The stacking and separation were performed by using phosphate buffer (25 mM, pH 2.5) containing 22% methanol and 100 mM SDS at -20 kV, and detected at 200 nm. During method validation, calibration plots were linear (r > or = 0.998) over a range of 30-3000 ng/mL for morphine, NM, and codeine, 100-2000 ng/mL for M6G, and 80-3200 ng/mL for M3G. The LODs (S/N = 5, sampling 600 s at 10 kV) were 10 ng/mL for morphine, NM, and codeine, 35 ng/mL for M6G, and 25 ng/mL for M3G. This stacking CE method could increase 2500-fold sensitivity of codeine, when comparing with CZE. Five addicts' urine specimens were analyzed. Their results were compared with those of LC-MS-MS, and showed good coincidence. This method could be feasible for monitoring morphine and its metabolites in forensic interest and pharmacokinetic investigations. 相似文献
936.
Huang TK Chen YC Ko HC Huang HW Wang CH Lin HK Chen FR Kai JJ Lee CY Chiu HT 《Langmuir : the ACS journal of surfaces and colloids》2008,24(11):5647-5649
A simple galvanic reduction for direct growth of Au nanowires on silicon wafers is developed. The nanowires were prepared by reacting HAuCl4aq with Sns in the presence of CTACaq (cetyltrimethylammonium chloride) and NaNO3aq, which were important to the product morphology development. The nanowire diameter was 50-100 nm, and the length was more than 20 microm. 相似文献
937.
Hydrodynamic flows in electrowetting 总被引:2,自引:0,他引:2
Hydrodynamic flows are generated inside a droplet in electrowetting when an ac voltage is applied. To discover the characteristics and origin of the flows, we investigated the flow pattern for a sessile droplet for various needle-electrode positions, electrolyte concentrations, and applied electrical frequencies. Two distinct types of flows were observed under current experimental conditions. In the typical experimental condition, a quite fast flow appears in the low-frequency range of about 10 Hz to 15 kHz. A different type of flow is observed in the high-frequency range of about 35 to 256 kHz, but this frequency range depends significantly on the electrolyte concentration. Most typically, the flow directions are different for the two flows. A shape oscillation of a droplet was observed in the low-frequency range by a high-speed camera. The flow in the low-frequency range is insensitive to the conductivity of the solution and may be caused by the interfacial oscillation of the droplet. The flow at high frequency is very sensitive to the conductivity of the solution and electrode position, so the high-frequency flow is believed to be caused by some electrohydrodynamic effect. 相似文献
938.
Minimalism in fabrication of self-organized nanogels holding both anti-cancer drug and targeting moiety 总被引:1,自引:0,他引:1
Kim S Park KM Ko JY Kwon IC Cho HG Kang D Yu IT Kim K Na K 《Colloids and surfaces. B, Biointerfaces》2008,63(1):55-63
Recent researches to develop nano-carrier systems in anti-cancer drug delivery have focused on more complicated design to improve therapeutic efficacy and to reduce side effects. Although such efforts have great impact to biomedical science and engineering, the complexity has been a huddle because of clinical and economic problems. In order to overcome the problems, a simplest strategy to fabricate nano-carriers to deliver doxorubicin (DOX) was proposed in the present study. Two significant subjects (i) formation of nanoparticles loading and releasing DOX and (ii) binding specificity of them to cells, were examined. Folic acid (FA) was directly coupled with pullulan (Pul) backbone by ester linkage (FA/Pul conjugate) and the degree of substitution (DS) was varied, which were confirmed by 1H NMR and UV spectrophotometry. Light scattering results revealed that the nanogels possessed two major size distributions around 70 and 270 nm in an aqueous solution. Their critical aggregation concentrations (CACs) were less than 10 microg/mL, which are lower than general critical micelle concentrations (CMCs) of low-molecular-weight surfactants. Transmission electron microscopy (TEM) images showed well-dispersed nanogel morphology in a dried state. Depending on the DS, the nanogels showed different DOX-loading and releasing profiles. The DOX release rate from FA8/Pul (with the highest DS) for 24h was slower than that from FA4/or FA6/Pul, indicating that the FA worked as a hydrophobic moiety for drug holding. Cellular uptake of the nanogels (KB cells) was also monitored by confocal microscopy. All nanogels were internalized regardless of the DS of FA. Based on the results, the objectives of this study, to suggest a new method overcoming the complications in the drug carrier design, were successfully verified. 相似文献
939.
940.
M. Rodová M. Liška K. Nitsch Z. Kožíšek 《Journal of Thermal Analysis and Calorimetry》2008,91(1):181-185
Solidification of molten zinc chloride was studied both experimentally and theoretically. By isothermal thermal analysis the
time needed for the melt to crystallize at a given temperature ranging between 453 and 553 K was determined and the data obtained
were compared with those of a calculated TTT curve. The extremum coordinates (temperature T
N, time t
N) of the curve, critical cooling rate v
CR, interfacial energy σ, and an additional parameter of kinetics barrier for nucleation ɛ were determined as T
N=508 K, t
N=7.29 s, v
CR=11.38 K s−1, σ=0.11956 J m−2 and ɛ=0.5712. By non-isothermal method the critical cooling rate of glass formation was determined as 1.25 K s−1. 相似文献