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991.
Miyaichi Y Nunomura N Kawata Y Kizu H Tomimori T Watanabe T Takano A Malla KJ 《Chemical & pharmaceutical bulletin》2006,54(1):136-138
From the underground parts of Eskemukerjea megacarpum HARA, two new stilbenes (14, 15) were isolated, together with a known coumarin, 5,7-dihydroxycoumarin (1), a tyramine derivative, trans-feruloyltyramine (2), two pyrogallol derivatives, gallic acid (3) and beta-glucogallin (4), four flavonoids, trifolin (5), hyperin (6), myricetin 3-O-beta-D-galactopyranoside (7), and myricitrin (8), five stilbenes, resveratorol (9), astringenin (10), piceid (11) astringin (12), and resveratorol 3-O-beta-D-(6-O-galloyl)glucopyranoside (13), a flavan-3-ol, (-)-epigallocatechin 3-O-gallate (16), two proanthocyanidins, catechin-(4alpha-->8)-epigallocatechin 3-O-gallate (17) and epicatechin 3-O-gallate-(4beta-->8)-epigallocatechin 3-O-gallate (18), and an anthocyanin, idaein (19). Compounds 14 and 15 were identified as (E)-3,5,3',4'-tetrahydroxystilbene 3-O-beta-D-(6-O-galloyl)glucopyranoside and (E)-3,5,4'-trihydroxystilbene 3-O-beta-D-(6-O-galloyl)glucopyranoside, respectively, based on spectral and chemical data. 相似文献
992.
Onuma K Watanabe A Kanzaki N Kubota T 《The journal of physical chemistry. B》2006,110(49):24876-24883
The intermolecular interaction and association dynamics of the Ynd1p protein were investigated using dynamic and time-resolved static light scattering measurements. The mutual diffusion coefficients of wild- and mutant-type (a single amino acid substitution) Ynd1p monomer were measured in 50 mM 2-(N-morpholino)ethanesulfonic acid (MES) buffer with 5 mM MnCl2 and 7.5% (v/v) ethylene glycol. Both translational diffusion coefficients at a zero protein concentration were (40.3 +/- 0.2) x 10(-12) m2/s at 20 degrees C and a pH of 7.0, so the hydrodynamic radius of the monomers was 4.1 +/- 0.1 nm. The measured intermolecular interaction between monomers, however, showed that the mutant-type Ynd1p had a stronger attractive force. Time-resolved static light scattering measurements showed that the association of mutant-type Ynd1p yielded a larger number of aggregates than that of wild-type Ynd1p. The time dependence of aggregate gyration radius differed between the two types. Fractal dimension analysis using scattering intensity data suggested that the inner structure of the aggregates changed from loose to rigid with time. Although this phenomenon is common for wild and mutant types, the differences in the number of aggregates yielded in the initial stages and in the intermolecular interaction affected the quality of the final grown crystals. That is, single crystals of Ynd1p grew in the mutant-type protein solution and polycrystals of Ynd1p grew in the wild-type protein solution. 相似文献
993.
Watanabe E Miyake S Baba K Eun H Endo S 《Analytical and bioanalytical chemistry》2006,386(5):1441-1448
This work describes the fundamental ability of a commercial ELISA to determine acetamiprid and the application of the ELISA
to residue analysis in fruit and vegetable samples. The ELISA exhibited satisfactory sensitivity (I
50 0.6 ng/g; limit of detection 0.053 ng/g) and a high selectivity for acetamiprid versus other neonicotinoid analogs (thiacloprid
amide). Methanol, which influenced the sensitivity of the ELISA the least, was selected as the extractant for the ELISA analysis.
Simple dilution of sample extracts with water eliminated matrix interferences. Average recoveries from the acetamiprid-spiked
agricultural samples were >95% using a simple extraction method. Analytical results obtained from the ELISA were comparable
to those obtained from the reference HPLC method (r>0.99). The ELISA applied to the residue analysis of acetamiprid in agricultural products is a rapid, simple, and cost-effective
method, and could be successfully applied to the detection of acetamiprid before the distribution of produce. 相似文献
994.
Hayakawa T Goseki R Kakimoto MA Tokita M Watanabe J Liao Y Horiuchi S 《Organic letters》2006,8(24):5453-5456
Wholly aromatic rod-rod type di- and triblock molecules, oligo(ether sulfone)-b-oligo(ether ketone)s (OES-OEK), were synthesized to study a solid-state self-assembled nanostructure. The OES and OEK segments in the block molecules form segregated crystalline domains. The energy-filtering transmission electron microscopy images revealed that the di- and triblock OES-OEK co-oligomers formed lamellar nanostructures with a periodicity of approximately 9 and 13 nm, respectively. [structure: see text]. 相似文献
995.
Nakamura T Vinodkumar AM Sugimoto T Aoi N Baba H Bazin D Fukuda N Gomi T Hasegawa H Imai N Ishihara M Kobayashi T Kondo Y Kubo T Miura M Motobayashi T Otsu H Saito A Sakurai H Shimoura S Watanabe K Watanabe YX Yakushiji T Yanagisawa Y Yoneda K 《Physical review letters》2006,96(25):252502
An exclusive measurement has been made of the Coulomb dissociation of the two-neutron halo nucleus 11Li at 70 MeV/nucleon at RIKEN. Strong low-energy (soft) E1 excitation is observed, peaked at about Ex = 0.6 MeV with B(E1) = 1.42(18) e2fm2 for Erel < or = 3 MeV, which was largely missed in previous measurements. This excitation represents the strongest E1 transition ever observed at such low excitation energies. The spectrum is reproduced well by a three-body model with a strong two-neutron correlation, which is further supported by the E1 non-energy-weighted cluster sum rule. 相似文献
996.
Shimoyamada A Tsuda S Ishizaka K Kiss T Shimojima T Togashi T Watanabe S Zhang CQ Chen CT Matsushita Y Ueda H Ueda Y Shin S 《Physical review letters》2006,96(2):026403
We have performed a vacuum ultraviolet laser excited photoemission spectroscopy on a d-electron heavy-fermion-like material LiV2O4 single crystal. We observed a sharp peak structure in the density of states at approximately 4 meV above the Fermi level (E(F)). The evolution of the peak height corresponds well with the crossover behavior to the heavy-fermion-like state as observed in the thermal and transport properties. The position, shape, and temperature (T) dependence of the peak structure is quite similar to the Kondo resonance observed in conventional f-electron heavy Fermion compounds. 相似文献
997.
We propose a new oxidation rate equation for silicon supposing only a diffusion of oxidizing species but not including any rate-limiting step by interfacial reaction. It is supposed that diffusivity is suppressed in a strained oxide region near SiO(2)/Si the interface. The expression of a parabolic constant in the new equation is the same as that of the Deal-Grove model, while a linear constant makes a clear distinction with that of the model. The estimated thickness using the new expression is close to 1 nm, which compares well with the thickness of the structural transition layers. 相似文献
998.
We consider a singular Cauchy problem for the Euler–Poisson–Darboux equation of Fuchsian type in the time variable with ramified Cauchy data. In this paper we establish an expansion of the solutions in a series of hypergeometric functions and then investigate the nature of the singularities of the solutions. 相似文献
999.
Lithuanian Mathematical Journal - Abstract. We show that, under the long-tailedness of the densities of normalized Lévy measures, the densities of infinitely divisible distributions on the... 相似文献
1000.
Kenji Watanabe Shigeru Negi Dr. Yukio Sugiura Prof. Dr. Akiko Kiriyama Dr. Akino Honbo Katsumi Iga Prof. Dr. Eiichi N. Kodama Dr. Takeshi Naitoh Masao Matsuoka Prof. Dr. Koji Kano Prof. Dr. 《化学:亚洲杂志》2010,5(4):825-834
Interactions of multivalent anionic porphyrins and their iron(III) complexes with cationic peptides, V3Ba‐L and V3IIIB, which correspond to those of the V3 loop regions of the gp120 envelope proteins of the HIV‐1Ba‐L and HIV‐1IIIB strains, respectively, are studied by UV/Vis, circular dichroism, 1H NMR, and EPR spectroscopy, a microcalorimetric titration method, and anti‐HIV assays. Tetrakis(3,5‐dicarboxylatophenyl)porphyrin (P1), tetrakis[4‐(3,5‐dicarboxylatophenylmethoxy)phenyl]porphyrin (P2), and their ferric complexes (FeIIIP1 and FeIIIP2) were used as the multivalent anionic porphyrins. P1 and FeIIIP1 formed stable complexes with both V3 peptides (binding constant K>106 M ?1) through combined electrostatic and van der Waals interactions. Coordination of the His residues in V3Ba‐L to the iron center of FeIIIP1 also played an important role in the complex stabilization. As P2 and FeIIIP2 form self‐aggregates in aqueous solution even at low concentrations, detailed analysis of their interactions with the V3 peptides could not be performed. To ascertain whether the results obtained in the model system are applicable to a real biological system, anti‐HIV‐1BA‐L and HIV‐1IIIB activity of the porphyrins is examined by multiple nuclear activation of a galactosidase indicator (MAGI) and 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide (MTT) assays. There is little correlation between chemical analysis and actual anti‐HIV activity, and the size rather than the number of the anionic groups of the porphyrin is important for anti‐HIV activity. All the porphyrins show high selectivity, low cytotoxicity, and high viral activity. FeIIIP1 and FeIIIP2 are used for the pharmacokinetic study. Half‐lives of these iron porphyrins in serum of male Wistar rats are around 4 to 6 h owing to strong interaction of these porphyrins with serum albumin. 相似文献