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51.
Casanova J Lamata L Egusquiza IL Gerritsma R Roos CF García-Ripoll JJ Solano E 《Physical review letters》2011,107(26):260501
We propose the quantum simulation of fermion and antifermion field modes interacting via a bosonic field mode, and present a possible implementation with two trapped ions. This quantum platform allows for the scalable add up of bosonic and fermionic modes, and represents an avenue towards quantum simulations of quantum field theories in perturbative and nonperturbative regimes. 相似文献
52.
Barber ZW Giorgetta FR Roos PA Coddington I Dahl JR Reibel RR Greenfield N Newbury NR 《Optics letters》2011,36(7):1152-1154
The optical frequency sweep of an actively linearized, ultrabroadband, chirped laser source is characterized through optical heterodyne detection against a fiber-laser frequency comb. Frequency sweeps were measured over approximately 5 THz bandwidths from 1530 nm to 1570 nm. The dominant deviation from linearity resulted from the nonzero dispersion of the fiber delay used as a reference for the sweep linearization. Removing the low-order dispersion effects, the residual sweep nonlinearity was less than 60 kHz rms, corresponding to a constant chirp with less than 15 ppb deviation across the 5 THz sweep. 相似文献
53.
54.
Jixin Qiao Petra Lagerkvist Ilia Rodushkin Susanna Salminen-Paatero Per Roos Syverin Lierhagen Karl Andreas Jensen Emma Engstrom Yann Lahaye Lindis Skipperud 《Journal of Radioanalytical and Nuclear Chemistry》2018,315(3):565-580
Inductively coupled plasma mass spectrometry (ICP-MS) techniques are widely used for determination of long-lived radionuclides and their isotopic ratios in the nuclear fields. Uranium (U) and Plutonium (Pu) isotopes have been determined by many researchers with ICP-MS due to its relatively high sensitivity and short measurement time. In this work, an inter-laboratory comparison exercise among the Nordic countries was performed, focusing on the measurement of U and Pu isotopes in certified reference materials by ICP-MS. The performance and characters of different ICP-MS instruments are evaluated and discussed in this paper. 相似文献
55.
Summary A method for the determination of low relative molecular mass carboxylic acids (C1–C4) in water is reported. The acids are converted to p-bromophenacyl esters prior to a glass-capillary gas chromatographic separation. By utilizing electron-caputre detection the detectability is substantially improved compared to flame-ionization detection. A comparison of three different ways to treat the water samples and to produce the derivatives is made. It is shown that the , p-dibromoacetophenone reagent decomposes to a small extent which limits the utility of the reagent. Nevertheless a detection limit for formic acid of approximately 2.5 mgl–1 is obtained. The method is applied to the determination of formic and acetic acids in a paper kraft water sample. 相似文献
56.
Widely tunable continuous-wave Raman laser in diatomic hydrogen pumped by an external-cavity diode laser 总被引:1,自引:0,他引:1
What is to the authors' knowledge the first experimental demonstration of a nonresonant cw Raman laser pumped by a tunable external-cavity diode laser (ECDL) is presented. The ECDL is phase-frequency locked to a high-finesse Raman laser cavity containing diatomic hydrogen (H(2)) by the Pound-Drever-Hall locking technique. The Stokes lasing threshold occurs at a pump power of 400 +/- 30 muW, and a maximum photon conversion efficiency of 12.0 +/- 1.3% is achieved at 1.6 mW of pump power. A 40-nm tuning range of the cw Stokes emission, 1174-1214 nm, is obtained by tuning of the wavelength of the ECDL pump source. 相似文献
57.
β-Amino ester enolate reacts readily with selected aldehydes and ketones. Deprotection via the N-oxide provides good yields of the 2-substituted acrylate ester. 相似文献
58.
Simone Portmann Hiu Ying Kwan Regula Theurillat Andrea Schmitz Meike Mevissen Wolfgang Thormann 《Journal of chromatography. A》2010,1217(51):7942-7948
Ketamine, a phencyclidine derivative, is used for induction of anesthesia, as an anesthetic drug for short term surgical interventions and in subanesthetic doses for postoperative pain relief. Ketamine undergoes extensive hepatic first-pass metabolism. Enantioselective capillary electrophoresis with multiple isomer sulfated β-cyclodextrin as chiral selector was used to identify cytochrome P450 enzymes involved in hepatic ketamine and norketamine biotransformation in vitro. The N-demethylation of ketamine to norketamine and subsequently the biotransformation of norketamine to other metabolites were studied via analysis of alkaline extracts of in vitro incubations of racemic ketamine and racemic norketamine with nine recombinantly expressed human cytochrome P450 enzymes and human liver microsomes. Norketamine was formed by CYP3A4, CYP2C19, CYP2B6, CYP2A6, CYP2D6 and CYP2C9, whereas CYP2B6 and CYP2A6 were identified to be the only enzymes which enable the hydroxylation of norketamine. The latter two enzymes produced metabolic patterns similar to those found in incubations with human liver microsomes. The kinetic data of ketamine N-demethylation with CYP3A4 and CYP2B6 were best described with the Michaelis–Menten model and the Hill equation, respectively. This is the first study elucidating the individual enzymes responsible for hydroxylation of norketamine. The obtained data suggest that in vitro biotransformation of ketamine and norketamine is stereoselective. 相似文献
59.
7-deaza-2,8-diaza-2'-deoxyadenosine (4) was synthesized from 8-aza-7-deaza-2'-deoxyadenosine (1) via the 1,N(6)-etheno derivative 5. Ring opening with sodium hydroxide followed by ring closure in the presence of sodium nitrite formed the tricyclic intermediate 5 from which the transiently introduced "etheno" moiety was removed with NBS. Compound 4 was converted to the phosphoramidite 11, which was employed in solid-phase oligonucleotide synthesis. Base pairing studies on 4, incorporated in a 12-mer duplex, showed that this adenine nucleoside analogue forms a strong base pair with dG but not with dT. This novel base pair is as stable as that of the canonical dA-dT pair. As a result of the absence of nitrogen-7 compound 4 is expected to form a face to face base pair with dG. 相似文献
60.
Roos C. W. van Lier Dr. A. Dowine de Bruijn Prof. Dr. Gerard Roelfes 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(4):1430-1437
Dehydroalanine (Dha) residues are attractive noncanonical amino acids that occur naturally in ribosomally synthesised and post-translationally modified peptides (RiPPs). Dha residues are attractive targets for selective late-stage modification of these complex biomolecules. In this work, we show the selective photocatalytic modification of dehydroalanine residues in the antimicrobial peptide nisin and in the proteins small ubiquitin-like modifier (SUMO) and superfolder green fluorescent protein (sfGFP). For this purpose, a new water-soluble iridium(III) photoredox catalyst was used. The design and synthesis of this new photocatalyst, [Ir(dF(CF3)ppy)2(dNMe3bpy)]Cl3, is presented. In contrast to commonly used iridium photocatalysts, this complex is highly water soluble and allows peptides and proteins to be modified in water and aqueous solvents under physiologically relevant conditions, with short reaction times and with low reagent and catalyst loadings. This work suggests that photoredox catalysis using this newly designed catalyst is a promising strategy to modify dehydroalanine-containing natural products and thus could have great potential for novel bioconjugation strategies. 相似文献