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41.
42.
Fifteen tetraalkylammonium salts of the functionalized sulfonic acids N,N-bis(2-hydroxy- ethyl)-2-aminoethanesulfonic acid, 2-(cyclohexylamino)ethanesulfonic acid and 2-hydroxy-4- morpholinopropanesulfonic acid were synthesized and the eight organic salts that were liquid at room temperature were characterized by physical, spectroscopic and chromatographic methods. All liquid salts were viscous at room temperature but after dilution with a suitable cosolvent could be used as mobile phases in liquid chromatography. For this application, the rapid deterioration of silica-based column packings was more of a deterrent than the physical properties of the salts. The tetraalkylammonium sulfonates had wide liquid ranges and were stable as column packings up to 150–180°C, making them suitable for use in gas chromatography. Their solvent properties were characterized by solvatochromic parameters [ET(30), π*, α and β] and by thermodynamic parameters determined by gas chromatography. Good agreement was found between the predictions of the two methods. The liquid salts showed strong orientation and solvent hydrogen bond acceptor capacity with weak hydrogen bond donor capacity in spite of the functionalization of the anions. The most probable reason for the weak hydrogen bond donor capacity of the anions is the unavailability of these functional groups for solute interactions owing to their preferential involvement in the formation of anion association complexes. The chemically defined structure, unique solvent properties and wide usable temperature ranges make the tetraalkylammonium sulfonates useful stationary phases for gas chromatography. 相似文献
43.
The system constants of the solvation parameter model are used to prepare system maps for the retention of small neutral compounds on an ethyl-bridged, ocatadecylsiloxane-bonded superficially porous silica stationary phase (Kinetex EVO C18) for aqueous mobile phases containing 10–70% (v/v) methanol or acetonitrile. Electrostatic interactions (cation-exchange) are important for the retention of weak bases with acetonitrile–water but not methanol–water mobile phase compositions. Compared with a superficially porous octadecylsiloxane-bonded silica stationary phase (Kinetex C18) with a similar morphology but different topology statistically significant differences in selectivity at the 95% confidence level are observed for neutral compounds that vary by size and hydrogen-bond basicity with other intermolecular interactions roughly similar. These selectivity differences are dampened with acetonitrile–water mobile phases, but are significant for methanol–water mobile phase compositions containing <30% (v/v) methanol. A comparison of a totally porous ethyl-bridged, octadecylsiloxane-bonded silica stationary phase (XBridge C18) with Kinetex EVO C18 indicated that they are effectively selectivity equivalent. 相似文献
44.
45.
O'Connell-Rodwell CE Wood JD Kinzley C Rodwell TC Poole JH Puria S 《The Journal of the Acoustical Society of America》2007,122(2):823-830
The ability to discriminate between call types and callers as well as more subtle information about the importance of a call has been documented in a range of species. This type of discrimination is also important in the vibrotactile environment for species that communicate via vibrations. It has recently been shown that African elephants (Loxodonta africana) can detect seismic cues, but it is not known whether they discriminate seismic information from noise. In a series of experiments, familiar and unfamiliar alarm calls were transmitted seismically to wild African elephant family groups. Elephants respond significantly to the alarm calls of familiar herds (p=0.004) but not to the unfamiliar calls and two different controls, thus demonstrating the ability of elephants to discriminate subtle differences between seismic calls given in the same context. If elephants use the seismic environment to detect and discriminate between conspecific calls, based on the familiarity of the caller or some other physical property, they may be using the ground as a very sophisticated sounding board. 相似文献
46.
M.P. Escudier J. OLeary R.J. Poole 《International Journal of Heat and Fluid Flow》2007,28(6):1418-1428
Numerical calculations have been carried out for flow in a truncated cone generated by rotation of one endwall. For both convergent (radius increasing with approach to the rotating endwall) and divergent geometries, vortex breakdown is suppressed beyond a certain angle of inclination of the sidewall. At the same time Moffat eddies of increasing strength and extent appear in the corner between the sidewall and the non-rotating endwall. For the divergent geometry, a zone of recirculation appears on the sidewall and eventually merges with the Moffat eddies. The flow phenomena identified from streamline patterns are consistent with the calculated variation of pressure around the periphery of the computational domain. 相似文献
47.
Jackson DR Mohareb A MacNeil J Razul MS Marangoni DG Poole PH 《The Journal of chemical physics》2011,134(20):204503
Using a 2D lattice model, we conduct Monte Carlo simulations of micellar aggregation of linear-chain amphiphiles having two solvophilic head groups. In the context of this simple model, we quantify how the amphiphile architecture influences the critical micelle concentration (CMC), with a particular focus on the role of the asymmetry of the amphiphile structure. Accordingly, we study all possible arrangements of the head groups along amphiphile chains of fixed length N = 12 and 16 molecular units. This set of idealized amphiphile architectures approximates many cases of symmetric and asymmetric gemini surfactants, double-headed surfactants, and boloform surfactants. Consistent with earlier results, we find that the number of spacer units s separating the heads has a significant influence on the CMC, with the CMC increasing with s for s < N/2. In comparison, the influence of the asymmetry of the chain architecture on the CMC is much weaker, as is also found experimentally. 相似文献
48.
Modglin JD Erdely VK Lin CY Coote ML Poole JS 《The journal of physical chemistry. A》2011,115(51):14687-14696
The energetics and kinetics of the reaction of variously substituted benzyl radicals with a model alkene were calculated at the G3(MP2)-RAD//B3-LYP/6-31G(d) level of theory to determine whether such reactions are amenable to Hammett analysis. The reactions were studied both in the gas phase and in toluene solution in the temperature range 298-353 K; calculations include 1D-hindered rotor corrections for low frequency torsional modes, and the solvation energies were calculated using COSMO-RS at the BP/TZP level of theory. The addition reaction was found to be dominated by radical stabilization effects, but under circumstances where olefin substituent effects were decoupled from aryl substituent effects, a modest polar effect comes into play, which is enhanced by solvation. Reasonable correlations with empirical substituent parameters such as Hammett σ and σ(?) are observed for the enthalpy of activation, but additional entropic factors act to decrease the degree of correlation with respect to free energies and rate coefficients, confirming hypotheses from earlier experimental work. Substituent effects on the reverse β-fragmentation reaction, and potential cyclization of the 3-phenylpropyl radicals formed by addition are also discussed. 相似文献
49.
Nirudodhi S Parsonage D Karplus PA Poole LB Maier CS 《International journal of mass spectrometry》2011,302(1-3):93-100
This is the first comprehensive HX-MS study of a "robust" 2-Cys peroxiredoxin (Prx), namely Salmonella typhimurium AhpC (StAhpC). Prx proteins control intracellular peroxide levels and are abundant antioxidant proteins in eukaryotes, archaea and bacteria. Crystal structural analyses and structure/activity studies of several bacterial and mammalian 2-Cys Prxs have revealed that the activity of 2-Cys Prxs is regulated by redox-dependent oligmerization and a sensitivity of the active site cysteine residue to overoxidation. The propensity to overoxidation is linked to the conformational flexibility of the peroxidatic active site loop. The HX-MS results emphasize the modulation of the conformational motility of the active site loop by disulfide formation. To obtain information on the conformational impact of decamer formation on the active site loop motility, mutants with Thr77 substituted by Ile, a decamer-disrupting mutation or by Val, a decamer-stabilizing mutation, were studied. For the isoleucine mutant, enhanced mobility was observed for regions encompassing the α4 helix located in the dimer-dimer interface and regions surrounding the peroxidatic loop. In contrast, the T77V mutation resulted in an increase in conformational stability in most regions of the protein except for the active site loop and the region encompassing the resolving cysteine. 相似文献
50.