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81.
Background
Growth cone migratory patterns show evidence of both deterministic and stochastic search modes. 相似文献82.
Gossauer A Nydegger F Kiss T Sleziak R Stoeckli-Evans H 《Journal of the American Chemical Society》2004,126(6):1772-1780
Two new types of optically active BODIPY fluorophores bearing chiral phenyl substituents either at the meso-position or at both external alpha-positions have been synthesized. Their chiroptical properties are strongly dependent both on the position of the chiral group and on the protonation of the chromophore. The solid-state structures of one of the difluoroboryl chelates bearing the chiral phenyl substituent at the meso-position (9a) as well as of the corresponding ligand (8a) and its perchlorate have been determined by X-ray diffraction analysis. These are, to the best of our knowledge, the first crystal structures of a dipyrrin free base and of a dipyrrin salt which have been obtained by X-ray diffraction analysis. Hence, for the first time, the helical structure of a protonated dipyrrin chromophore has been proved experimentally. 相似文献
83.
Alkali-stable, high-pI isoelectric membranes have been synthesized from quaternary ammonium derivatives of cyclodextrins and poly(vinyl alcohol), and bifunctional cross-linkers, such as glycerol-1,3-diglycidyl ether. The new, high-pI isoelectric membranes were successfully applied as cathodic membranes in isoelectric trapping separations in place of the hydrolytically more labile, polyacrylamide-based cathodic isoelectric membranes, and permitted the use of catholytes as alkaline as 1 M NaOH. The new high-pI isoelectric membranes have shown excellent mechanical stability, low electric resistance and long life times, even when subjected to electrophoresis with current densities as high as 80 mA/cm2. 相似文献
84.
85.
Alonso AM Horcajada R Groombridge HJ Mandalia R Motevalli M Utley JH Wyatt PB 《Chemical communications (Cambridge, England)》2004,(4):412-413
Electrochemical reduction of enantiomerically pure amino- and alkoxy-phenazine derivatives forms strongly basic radical anions which give asymmetric induction in the conversion of 3,4-epoxytetrahydrothiophene-1,1-dioxide into the allylic ester with facile regeneration of the phenazine. 相似文献
86.
Helen O. Leung Oluwatoyin M. Ibidapo Mary B. Bianchi 《Journal of Molecular Spectroscopy》2003,222(1):3-14
The rotational spectra of six isotopomers of the linear and bent isomers of HF-N2O have been collected in the 7-18 GHz region with a Fourier transform microwave spectrometer. The nuclear hyperfine structure in the spectra produced by HF spin-spin coupling interaction and nuclear quadrupole coupling interactions due to the D nucleus of DF and the nuclei of N2O have been resolved and analyzed. In the linear isomer, H in HF is bonded to the terminal N in N2O. The NF bond lengths are 2.9808(2) Å for the HF-containing isotopomers and 2.9732(2) Å for the DF-containing isotopomers. The zero point angles are 23.1° for HF and 31-34° for N2O. The hyperfine constants suggest that the HF bond is lengthened by 0.0105 Å upon complexation and that the electric field gradients of the two nitrogen nuclei in N2O are perturbed differently in the complex. In the bent isomer, the hydrogen bond is formed between HF and O in N2O. The intermolecular distances are 3.4942(2) Å for the HF-containing isotopomers and 3.4436(2) Å for the DF-containing isotopomers, with HF and N2O forming angles of 34° and 46°, respectively, with the intermolecular axis. The nuclear quadrupole coupling constants of the two nitrogen nuclei do not indicate electric field gradient perturbation in this isomer. 相似文献
87.
Skaropoulos NC Yagridou HD Chrissoulidis DP 《The Journal of the Acoustical Society of America》2003,113(6):3001-3011
An exact, analytical solution is developed for the problem of acoustic-wave scattering from a cluster of ideal, gaseous, spherical bubbles in an unbounded, homogeneous, host fluid. This solution takes into account all modes of oscillation of the bubbles as well as all interactions between them; it is applicable to a wide range of bubble sizes and excitation frequencies. In the low frequency regime, the theory of this paper is shown to reduce to the "monopole" approximation, the effect of higher-order modes being non-negligible only for very small bubble-to-bubble separations. A numerical study of interactive backscattering from small clusters, comprising up to three ideal bubbles, is presented. Interactions between the bubbles are shown to produce downward shifts in the resonance frequency of the cluster, when the scattering configuration is symmetric. Furthermore, asymmetries of the scattering configuration are shown to generate sharp resonances at frequencies above the resonance of the symmetric mode. The results of this paper agree with previous theoretical and experimental work. 相似文献
88.
Murrie M Biner D Stoeckli-Evans H Güdel HU 《Chemical communications (Cambridge, England)》2003,(2):230-231
The role of temperature in the formation of high nuclearity nickel(II) citrate spin clusters is explored, revealing how changes in structure and hence magnetic properties can be triggered through desolvation and ligand reorganisation. 相似文献
89.
Hervé G Hahn DU Hervé AC Goodworth KJ Hill AM Hailes HC 《Organic & biomolecular chemistry》2003,1(2):427-435
Methodologies to access water soluble large ringed calixarenes in good yield using efficient synthetic procedures have been investigated. Symmetrical partial functionalisations at the lower rim are described using activated [n]ethylene glycol chains and the addition behaviour contrasted with that of bromoalkanenitriles which proceeds with no observed regioselectivity. Full functionalisations of the calixarenes bearing hydrophilic groups are then investigated and a two-step procedure established which appears to be generally applicable for the addition of different [n]ethylene glycol chains. Furthermore, difunctionalisation under different reaction conditions are described. Throughout, strategies for the characterisation of these high mass compounds are outlined. 相似文献
90.
[reaction: see text] The conjugate addition of dithiols to bis-ynones generates a versatile masked 1,3,5-triketone platform. These functional units are useful intermediates for the synthesis of oxygen-containing heterocycles commonly found in polyketide natural products. The tetrahydropyranyl fragments of the marine macrolides Lyngbouilloside and Callipeltoside A have been synthesized with use of this methodology. 相似文献