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101.
Dr. Abdulghani Ismail Dr. Silvia Voci Lucie Descamps Dr. Arnaud Buhot Prof. Dr. Neso Sojic Dr. Loïc Leroy Dr. Aurélie Bouchet-Spinelli 《Chemphyschem》2021,22(11):1094-1100
This work depicts the original combination of electrochemiluminescence (ECL) and bipolar electrochemistry (BPE) to map in real-time the oxidation of silicon in microchannels. We fabricated model silicon-PDMS microfluidic chips, optionally containing a restriction, and monitored the evolution of the surface reactivity using ECL. BPE was used to remotely promote ECL at the silicon surface inside microfluidic channels. The effects of the fluidic design, the applied potential and the resistance of the channel (controlled by the fluidic configuration) on the silicon polarization and oxide formation were investigated. A potential difference down to 6 V was sufficient to induce ECL, which is two orders of magnitude less than in classical BPE configurations. Increasing the resistance of the channel led to an increase in the current passing through the silicon and boosted the intensity of ECL signals. Finally, the possibility of achieving electrochemical reactions at predetermined locations on the microfluidic chip was investigated using a patterning of the silicon oxide surface by etched micrometric squares. This ECL imaging approach opens exciting perspectives for the precise understanding and implementation of electrochemical functionalization on passivating materials. In addition, it may help the development and the design of fully integrated microfluidic biochips paving the way for development of original bioanalytical applications. 相似文献
102.
Kobra Mahdavipour Mahshid Khazaei Shadfar Hossein Rangani Jahromi Roberto Morandotti Rosario Lo Franco 《Entropy (Basel, Switzerland)》2022,24(3)
A witness of non-Markovianity based on the Hilbert–Schmidt speed (HSS), a special type of quantum statistical speed, has been recently introduced for low-dimensional quantum systems. Such a non-Markovianity witness is particularly useful, being easily computable since no diagonalization of the system density matrix is required. We investigate the sensitivity of this HSS-based witness to detect non-Markovianity in various high-dimensional and multipartite open quantum systems with finite Hilbert spaces. We find that the time behaviors of the HSS-based witness are always in agreement with those of quantum negativity or quantum correlation measure. These results show that the HSS-based witness is a faithful identifier of the memory effects appearing in the quantum evolution of a high-dimensional system with a finite Hilbert space. 相似文献
103.
P. Olivero G. Amato F. Bellotti S. Borini A. Lo Giudice F. Picollo E. Vittone 《The European Physical Journal B - Condensed Matter and Complex Systems》2010,75(2):127-132
In the present work we report about the investigation of the conduction mechanism of sp2 carbon micro-channels in single crystal diamond. The structures are fabricated with a technique which employs a MeV focused
ion-beam to damage diamond in conjunction with variable thickness masks. This process changes significantly the structural
properties of the target material, because the ion nuclear energy loss induces carbon conversion from sp3 to sp2 state mainly at the end of range of the ions (few micrometers). Furthermore, placing a mask with increasing thickness on
the sample it is possible to modulate the channels depth at their endpoints, allowing their electrical connection with the
surface. A single-crystal HPHT diamond sample was implanted with 1.8 MeV He+ ions at room temperature, the implantation fluence was set in the range 2.1×1016-6.3×1017 ions cm-2, determining the formation of micro-channels with a graded level of damage extending down to a depth of about 3 μm. After
deposition of metallic contacts at the channels’ endpoints, the electrical characterization was performed measuring the I-V
curves at variable temperatures in the 80-690 K range. The Variable Range Hopping model was used to fit the experimental data
in the ohmic regime, allowing the estimation of characteristic parameters such as the density of localized states at the Fermi
level. A value of 5.5×1017 states cm-3 eV-1 was obtained, in satisfactory agreement with values previously reported in literature. The power-law dependence between current
and voltage is consistent with the space charge limited mechanism at
moderate electric fields. 相似文献
104.
105.
We demonstrate that massless QED in three dimensions contains endemic infrared divergences. It is argued that these divergences do not affect observables; furthermore, it is possible to choose a gauge that renders the theory finite. 相似文献
106.
The magnetic behaviour and martensitic transformation at cryogenic temperatures (down to 4 K) of the austenite phase of the duplex stainless steel (DSS), 7MoPLUS, were studied. As regards the prediction of Neel temperature, the empirical expressions for austenitic stainless steels are not applicable to the austenite phase of 7MoPLUS, although the composition of the austenite phase falls within the composition ranges within which the expressions were developed. Regarding the prediction of martensitic point Ms, the applicability of ‘old’ and recently developed expressions has been examined. The recently developed expressions, which take into account more alloying elements and their interactions, are not suitable for the austenite phase of 7MoPLUS. But for the ‘old’, simpler expressions, they seem to be valid in the sense that they all predict high stability of the austenite phase. Results obtained from 7MoPLUS were qualitatively the same as those obtained from another DSS, designated as 2205. Reasons for the applicability and inapplicability of these empirical expressions are suggested. 相似文献
107.
Irradiation of 3-(4-substituted styryl)furans in basic media yielded a series of 7-substituted-2-methylnaphthalenes, including methoxy, isopropyl, ethyl, methyl, fluoro, and cyano substituents. This base-induced photorearrangement involves cis-trans photoisomerization, 6e photocyclization, base-induced elimination, and a Norrish Type I photoreaction and is a novel method to synthesize unsymmetrical 2,7-disubstituted naphthalenes. 相似文献
108.
109.
Jiunn-Liang Lin Jiunn-Guang Lo Ren-Shyan Liu Ai-Yih Wang 《Journal of Radioanalytical and Nuclear Chemistry》2010,285(3):531-538
Tolonium chloride is a common reagent in the diagnosis of oral premalignant and malignant lesions. This study establishes the optimal preparation of radioiodinated tolonium chloride (RTC) and evaluate its radiochemical and biological characteristics. Instant thin layer chromatography (ITLC), ion exchange chromatography (IC), paper electrophoresis, and the effect of pH on labeling efficiency revealed the chemical characterization of RTC. Biodistribution, blood clearance, urinary excretion, toxic effect, and Lugol’s solution effect on the thyroid uptake of RTC revealed RTCs biological characteristics. The optimal labeling condition was pH = 2.96 after 15 h stirring, the labeling efficiency was 60%. After purification by IC, the radiochemical purity of RTC was 94%, and the shelf life of RTC was at least 90 days. In the biodistribution study, the liver was major target organs, approximated 6.11% of injected dose accumulate in per gram of tissue (6.11% ID/g) at 10 min after injection. The tissue-to-blood radioactivity ratio significant (p < 0.05) increased with reaction time. In liver, the tissue-to-blood radioactivity ratio was 2.2 ± 0.51 at 10 min after injection, and increased to 22.4 ± 4.52 at 120 min after injection. The blood clearance study showed a significant decrease in blood radioactivity. The radioactivity in the blood was about 2.76% of the injected dose per milliliter blood at 10 min post-injection, but decreased to 0.12% at 120 min post-injection. Lugol’s solution does not affect the thyroid uptake of RTC. Almost all the administered RTC recovered at 60 h after injection, with 79% recovered in feces and 17% recovered in urine. This study shows that RTC is non-toxic, and may be suitable as a liver imaging agent. 相似文献
110.
Structural Manipulation of Ruthenium(II) Polypyridine Nitrone Complexes to Generate Phosphorogenic Bioorthogonal Reagents for Selective Cellular Labeling 下载免费PDF全文
Tommy Siu‐Ming Tang Dr. Hua‐Wei Liu Prof. Kenneth Kam‐Wing Lo 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(28):9649-9659
We report a new class of ruthenium(II) polypyridine complexes functionalized with a nitrone group as phosphorogenic bioorthogonal probes. These complexes were very weakly emissive owing to rapid C=N isomerization of the nitrone moiety, but exhibited significant emission enhancement upon strain‐promoted alkyne–nitrone cycloaddition (SPANC) reaction with bicyclo[6.1.0]nonyne (BCN)‐modified substrates. The modification of nitrone with a dicationic ruthenium(II) polypyridine unit at the α‐C‐position and a phenyl ring at the N‐position led to remarkably accelerated reaction kinetics, which are substantially greater (up to ≈278 fold) than those of other acyclic nitrone–BCN systems. Interestingly, the complexes achieved specific cell membrane/cytosol staining upon specific labeling of an exogenous substrate, BCN‐modified decane (BCN‐C10), in live cells. Importantly, the in situ generation of the more lipophilic isoxazoline adduct in the cytoplasm resulted in increased cytotoxicity, highlighting a novel approach to apply the SPANC labeling technique in drug activation. 相似文献